Page last updated: 2024-10-25

deferoxamine and Thalassemias

deferoxamine has been researched along with Thalassemias in 488 studies

Deferoxamine: Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
desferrioxamine B : An acyclic desferrioxamine that is butanedioic acid in which one of the carboxy groups undergoes formal condensation with the primary amino group of N-(5-aminopentyl)-N-hydroxyacetamide and the second carboxy group undergoes formal condensation with the hydroxyamino group of N(1)-(5-aminopentyl)-N(1)-hydroxy-N(4)-[5-(hydroxyamino)pentyl]butanediamide. It is a siderophore native to Streptomyces pilosus biosynthesised by the DesABCD enzyme cluster as a high affinity Fe(III) chelator.

Research Excerpts

ExcerptRelevanceReference
" The iron chelator deferiprone is frequently used in individuals with thalassemia syndromes, but data in patients with SCD are limited."9.51Deferiprone vs deferoxamine for transfusional iron overload in SCD and other anemias: a randomized, open-label noninferiority study. ( Adly, AAM; Alshehri, A; Badr, M; Ebeid, FSE; El-Beshlawy, A; Elalfy, MS; Hamdy, M; Inusa, B; Kanter, J; Kilinc, Y; Kwiatkowski, JL; Lee, D; Tricta, F; Williams, S, 2022)
"The possible healing effect of deferoxamine and pentoxifylline on persisting lower limb ulcers was studied in 51 patients with thalassemia major."9.07Effect of pentoxifylline on treatment of lower limb ulcers in patients with thalassemia major. ( Angastiniotis, C; Angelides, NS; Pavlides, N, 1992)
"Deferasirox (DFX) has recently been used to treat thalassemia with iron overload; however, its long-term effectiveness and safety await multi-year studies."9.01Effectiveness and Safety of Deferasirox in Thalassemia with Iron Overload: A Meta-Analysis. ( Chen, G; Dou, H; Qin, Y; Zhao, Y, 2019)
"To assess the effectiveness and safety of oral deferasirox in people with thalassaemia and iron overload."8.95Deferasirox for managing iron overload in people with thalassaemia. ( Allert, R; Bassler, D; Bollig, C; Meerpohl, JJ; Motschall, E; Niemeyer, CM; Rücker, G; Schell, LK, 2017)
"A meta-analysis was conducted to investigate the efficacy and safety of three main iron chelators, namely, deferoxamine (DFO), deferiprone (DFP) and deferasirox (DFX) for thalassemia major (TM) patients."8.89Comparative efficacy and safety of deferoxamine, deferiprone and deferasirox on severe thalassemia: a meta-analysis of 16 randomized controlled trials. ( Huang, L; Jiang, H; Xia, S; Zhang, W, 2013)
"To assess the effectiveness and safety of oral deferasirox in people with thalassaemia and secondary iron overload."8.88Deferasirox for managing iron overload in people with thalassaemia. ( Antes, G; Bassler, D; Fleeman, N; Meerpohl, JJ; Motschall, E; Niemeyer, CM; Rücker, G, 2012)
"Deferiprone (L1), and appropriate combinations with deferoxamine (DFO), can be used effectively for the treatment of thalassemia and other transfusional iron loading conditions."8.83Future chelation monotherapy and combination therapy strategies in thalassemia and other conditions. comparison of deferiprone, deferoxamine, ICL670, GT56-252, L1NAll and starch deferoxamine polymers. ( Kontoghiorghes, GJ, 2006)
"The role of the orally active iron (Fe) chelator deferiprone in the treatment of beta-thalassemia remains a controversial subject."8.81The controversial role of deferiprone in the treatment of thalassemia. ( Richardson, DR, 2001)
"The newly available iron chelator deferasirox (Exjade, Novartis) is expected to provide better long-term clinical outcomes and improved quality of life for patients with thalassemia than its predecessor, deferoxamine (Desferal, Novartis), because of its oral tablet form."7.79A pharmaco-economic evaluation of deferasirox for treating patients with iron overload caused by transfusion-dependent thalassemia in Taiwan. ( Chang, HH; Chung, KP; Ho, WL; Jou, ST; Lin, DT; Lin, KH; Lu, MY; Yang, SS; Yang, YL, 2013)
"The Thalassemia Clinical Research Network collected adherence information from 79 patients on deferoxamine and 186 on deferasirox from 2007 to 2009."7.77Iron chelation adherence to deferoxamine and deferasirox in thalassemia. ( Coates, T; Giardina, PJ; Haines, D; Kwiatkowski, J; Mednick, L; Neufeld, EJ; Olivieri, N; Pakbaz, Z; Porter, J; Sobota, A; Thompson, AA; Trachtenberg, F; Vichinsky, E; Yamashita, R, 2011)
"In this report we firstly describe a case of reactivation of hepatitis B virus (HBV) replication occurred in a patient affected by Thalassemia major which underwent a combined chelation therapy with desferioxamine (DFO) and deferiprone (DFP)."7.75Hepatitis B virus reactivation during combined therapy with deferiprone and desferioxamine in a hepatitis B surface antigen thalassemic carrier. ( Ammirabile, M; Cinque, P; Di Matola, T; Lanza Galeota, A; Prossomariti, L; Ricchi, P, 2009)
" The known predisposing factors of infection include prior splenectomy, iron overload and use of iron chelator such as deferoxamine (DFO)."7.75Effects of chelators (deferoxamine, deferiprone and deferasirox) on the growth of Klebsiella pneumoniae and Aeromonas hydrophila isolated from transfusion-dependent thalassemia patients. ( Chan, GC; Chan, S; Ha, SY; Ho, PL, 2009)
"Deferoxamine mesylate (DFO) reduces morbidity and mortality associated with transfusional iron overload."7.74Outcomes, utilization, and costs among thalassemia and sickle cell disease patients receiving deferoxamine therapy in the United States. ( Baladi, JF; Coates, TD; Delea, TE; Hagiwara, M; Phatak, PD; Thomas, SK, 2008)
"For the past 2-6 years, two groups of thalassemia patients, one of 16 patients on deferoxamine (DFO) monotherapy (35-80 mg/kg, 2-5 days/week) and the other group comprising 19 patients on a deferiprone (L1) and DFO combination therapy (L1 75-100 mg/kg/day and DFO 30-60 mg/kg, 1-5 days/week), have been studied and compared before and after the introduction of the combination therapy."7.74Long term comparative studies in thalassemia patients treated with deferoxamine or a deferoxamine/deferiprone combination. Identification of effective chelation therapy protocols. ( Economides, C; Eracleous, E; Kolnagou, A; Kontoghiorghes, GJ, 2008)
"A number of studies have shown that regular chelation therapy with deferoxamine is effective in patients with secondary hemochromatosis."7.69[Long-term efficacy of subcutaneous administration of deferoxamine in patients with secondary hemochromatosis]. ( Fujisawa, S; Kobayashi, M; Yano, K, 1996)
"To assess the effects of deferoxamine (DFO) on the kidneys, we studied 27 patients with thalassemia major on chronic subcutaneous (s."7.68The effects of subcutaneous deferoxamine administration on renal function in thalassemia major. ( Bentur, Y; Kochavi-Atiya, Y; Koren, G; Olivieri, NF, 1991)
"Metaphyseal irregularity and abnormal vertebral bodies resembling a bone dysplasia were seen in two of five children with thalassemia major who were begun on a regimen of hypertransfusion and chelation with deferoxamine before the age of 3 years."7.68Deferoxamine-induced bone dysplasia in patients with thalassemia major. ( Brill, PW; Cunningham-Rundles, S; Giardina, PJ; Winchester, P, 1991)
"To determine whether survival of patients with beta-thalassemia major has been prolonged by management that utilizes hypertransfusion and chelation with deferoxamine, we analyzed longevity by the Kaplan-Meier product-limit method."7.68Prolonged survival in patients with beta-thalassemia major treated with deferoxamine. ( Ehlers, KH; Engle, MA; Giardina, PJ; Hilgartner, MW; Lesser, ML, 1991)
"Eight patients with transfusion-dependent thalassemia major were given continuous intravenous infusions of the chelator, deferoxamine mesylate, to reduce iron overload."7.68Pulmonary syndrome in patients with thalassemia major receiving intravenous deferoxamine infusions. ( Freedman, MH; Grisaru, D; MacLusky, I; Olivieri, N; Thorner, PS, 1990)
"We examined the efficacy of long-term subcutaneous deferoxamine therapy in the prevention of iron-related cardiac disease in patients with thalassemia major who began treatment after the age of 10 years."7.67Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major. ( Colan, S; Freedman, MH; Nathan, DG; Olivieri, N; Propper, R; Rose, V; Sallan, D; Wolfe, L, 1985)
"We evaluated decreasing deferoxamine-induced urinary iron excretion during intensive chelation therapy in four children with thalassemia."7.66Response to long-term deferoxamine therapy in thalassemia. ( Cohen, A; Martin, M; Schwartz, E, 1981)
"Iron overload is the primary cause of mortality and morbidity in thalassemia major despite advances in chelation therapy."6.78Combined chelation therapy with deferasirox and deferoxamine in thalassemia. ( Evans, P; Harmatz, P; Kurio, G; Lal, A; Neumayr, L; Ng, V; Porter, J; Sweeters, N; Vichinsky, E, 2013)
" There was no significant difference in the proportion of patients with adverse events in the two therapy groups although the nature of the adverse events differed according to the chelation regimen."6.72A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemia. ( Fischer, R; Galanello, R; Kattamis, A; Ladis, V; Leoni, G; Lund, U; Piga, A; Tricta, F; Voi, V, 2006)
"The most frequent side effects were joint pain, stiffness or swelling in 6 patients (35."6.69Efficacy and side effects of deferiprone (L1) in thalassemia patients not compliant with desferrioxamine. ( Chamoun, FM; Khoriaty, AI; Koussa, S; Mourad, FH; Neeman, R; Saad, MA; Taher, A, 1999)
" Selected protocols using DFO, L1, and their combination can be designed for personalized chelation therapy in TI, which can effectively and safely remove all the excess toxic iron and prevent cardiac, liver, and other organ damage."6.53Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. ( Kontoghiorghe, CN; Kontoghiorghes, GJ, 2016)
"Iron overload is a major complication of transfusion-dependent thalassemia (TDT) and requires iron chelation (IC) therapy."5.62Using of deferasirox and deferoxamine in refractory iron overload thalassemia. ( Buaboonnam, J; Narkbunnam, N; Phuakpet, K; Pongtanakul, B; Sanpakit, K; Takpradit, C; Vathana, N; Viprakasit, V, 2021)
"Reversal of arrhythmia to sinus rhythm was noted in all patients."5.56Combined chelation with high-dose deferiprone and deferoxamine to improve survival and restore cardiac function effectively in patients with transfusion-dependent thalassemia presenting severe cardiac complications. ( Chao, YH; Chuang, TY; Li, JP; Weng, TF; Wu, KH, 2020)
" The iron chelator deferiprone is frequently used in individuals with thalassemia syndromes, but data in patients with SCD are limited."5.51Deferiprone vs deferoxamine for transfusional iron overload in SCD and other anemias: a randomized, open-label noninferiority study. ( Adly, AAM; Alshehri, A; Badr, M; Ebeid, FSE; El-Beshlawy, A; Elalfy, MS; Hamdy, M; Inusa, B; Kanter, J; Kilinc, Y; Kwiatkowski, JL; Lee, D; Tricta, F; Williams, S, 2022)
"Deferoxamine was given intravenously for 12 months and subcutaneously in the next 18 months."5.26[Role and therapeutic use of deferoxamine in iron overload due to thalassemia (author's transl)]. ( Bachelot, C; Bost, M; Joannard, A; Lévy, G, 1980)
"  Transfusional iron overload in patients with thalassaemia could be reduced to normal body iron range levels using effective deferiprone/deferoxamine combinations."5.14Reduction of body iron stores to normal range levels in thalassaemia by using a deferiprone/deferoxamine combination and their maintenance thereafter by deferiprone monotherapy. ( Kleanthous, M; Kolnagou, A; Kontoghiorghes, GJ, 2010)
" The following prospective, randomized trial was carried out to determine the effectiveness, in children and young adults, of combined deferiprone (DFP) and deferoxamine (DFO) in reducing transfusional iron overload compared to either drug alone and to assess the safety and tolerability of DFP."5.13Iron chelation in thalassemia: combined or monotherapy? The Egyptian experience. ( El-Beshlawy, A; Eltagui, M; Hamdy, M; Hoffbrand, AV; Manz, C; Mostafa, A; Naja, M; Shaker, O; Sharaf, I; Sobh, H; Taher, A; Tarabishi, C; Youssry, I, 2008)
"The possible healing effect of deferoxamine and pentoxifylline on persisting lower limb ulcers was studied in 51 patients with thalassemia major."5.07Effect of pentoxifylline on treatment of lower limb ulcers in patients with thalassemia major. ( Angastiniotis, C; Angelides, NS; Pavlides, N, 1992)
"Deferasirox (DFX) has recently been used to treat thalassemia with iron overload; however, its long-term effectiveness and safety await multi-year studies."5.01Effectiveness and Safety of Deferasirox in Thalassemia with Iron Overload: A Meta-Analysis. ( Chen, G; Dou, H; Qin, Y; Zhao, Y, 2019)
"To compare the efficacy and safety of desferrioxamine (DFO), deferiprone (DFP), deferasirox (DFX) and silymarin in patients with either thalassemia or sickle cell disorder through network meta-analysis."4.98Efficacy and safety of iron chelators in thalassemia and sickle cell disease: a multiple treatment comparison network meta-analysis and trial sequential analysis. ( Sivaramakrishnan, G; Sridharan, K, 2018)
"To assess the effectiveness and safety of oral deferasirox in people with thalassaemia and iron overload."4.95Deferasirox for managing iron overload in people with thalassaemia. ( Allert, R; Bassler, D; Bollig, C; Meerpohl, JJ; Motschall, E; Niemeyer, CM; Rücker, G; Schell, LK, 2017)
"Desferrioxamine is the recommended first-line therapy for iron overload in people with thalassaemia major and deferiprone or deferasirox are indicated for treating iron overload when desferrioxamine is contraindicated or inadequate."4.89Desferrioxamine mesylate for managing transfusional iron overload in people with transfusion-dependent thalassaemia. ( Brunskill, SJ; Chowdhury, O; Doree, C; Fisher, SA; Gooding, S; Roberts, DJ, 2013)
"In the absence of data from randomised controlled trials, there is no evidence to suggest the need for a change in current treatment recommendations; namely that deferiprone is indicated for treating iron overload in people with thalassaemia major when desferrioxamine is contraindicated or inadequate."4.89Oral deferiprone for iron chelation in people with thalassaemia. ( Brunskill, SJ; Chowdhury, O; Doree, C; Fisher, SA; Gooding, S; Roberts, DJ, 2013)
"A meta-analysis was conducted to investigate the efficacy and safety of three main iron chelators, namely, deferoxamine (DFO), deferiprone (DFP) and deferasirox (DFX) for thalassemia major (TM) patients."4.89Comparative efficacy and safety of deferoxamine, deferiprone and deferasirox on severe thalassemia: a meta-analysis of 16 randomized controlled trials. ( Huang, L; Jiang, H; Xia, S; Zhang, W, 2013)
"To assess the effectiveness and safety of oral deferasirox in people with thalassaemia and secondary iron overload."4.88Deferasirox for managing iron overload in people with thalassaemia. ( Antes, G; Bassler, D; Fleeman, N; Meerpohl, JJ; Motschall, E; Niemeyer, CM; Rücker, G, 2012)
"We found no reason to change current treatment recommendations, namely deferiprone is indicated for treating iron overload in people with thalassaemia major when desferrioxamine is contraindicated or inadequate."4.84Oral deferiprone for iron chelation in people with thalassaemia. ( Brunskill, SJ; Doree, C; Howard, J; Hyde, CJ; Roberts, DJ; Williams, S, 2007)
"The iron chelators deferoxamine (DFO) and deferiprone (L1) have demonstrated their ability to normalize cardiac function in patients with iron overload-induced cardiac disease."4.84Effects of chelation therapy on cardiac function improvement in thalassemia patients: literature review and the Taiwanese experience. ( Peng, CT; Tsai, CH; Wu, KH, 2008)
"Deferiprone (L1), and appropriate combinations with deferoxamine (DFO), can be used effectively for the treatment of thalassemia and other transfusional iron loading conditions."4.83Future chelation monotherapy and combination therapy strategies in thalassemia and other conditions. comparison of deferiprone, deferoxamine, ICL670, GT56-252, L1NAll and starch deferoxamine polymers. ( Kontoghiorghes, GJ, 2006)
"Therapy with either deferiprone (DFP) or deferoxamine (DFO) is inadequate in achieving negative iron balance in many patients with thalassemia."4.82Combined therapy with deferoxamine and deferiprone. ( Kattamis, A, 2005)
"In patients with thalassemia, the assessment of liver iron concentration (LIC) can be used to initiate chelation treatment with desferrioxamine (DFO), deferiprone (DFP), or novel chelators (deferasirox); to adjust chelation dose according to the actual blood transfusion rate; and to monitor chelation efficacy."4.82Monitoring long-term efficacy of iron chelation treatment with biomagnetic liver susceptometry. ( Fischer, R; Harmatz, P; Nielsen, P; Piga, A, 2005)
"The role of the orally active iron (Fe) chelator deferiprone in the treatment of beta-thalassemia remains a controversial subject."4.81The controversial role of deferiprone in the treatment of thalassemia. ( Richardson, DR, 2001)
" Such is the case for iron chelating agents used in transfusion-dependent patients of Thalassemia, of which deferoxamine (DFO) is the most widely used."4.31Lifting the iron curtain of vision. ( Rosin, B; Sahel, JA, 2023)
"We report two cases of bilateral macular pattern dystrophy in transfusion dependent patients undergoing chronic chelation therapy with deferoxamine due to thalassemias."3.88Pattern dystrophies in patients treated with deferoxamine: report of two cases and review of the literature. ( Georgakopoulos, CD; Kostopoulou, EV; Makri, OE; Tsapardoni, F, 2018)
" Time after splenectomy >10 years, deferoxamine therapy, and iron overload may be clinical risk factors for severe bacterial infection in patients with NTDT."3.81Severe bacterial infections in patients with non-transfusion-dependent thalassemia: prevalence and clinical risk factors. ( Chansung, K; Jetsrisuparb, A; Sirijerachai, C; Teawtrakul, N; Wanitpongpun, C, 2015)
"A 34-year-old man with thalassemia major complained of nyctalopia and decreased vision following high-dose intravenous deferoxamine to treat systemic iron overload."3.80Deferoxamine retinopathy: spectral domain-optical coherence tomography findings. ( Chen, YH; Lai, CC; Wu, CH; Wu, WC; Yang, CP, 2014)
"The newly available iron chelator deferasirox (Exjade, Novartis) is expected to provide better long-term clinical outcomes and improved quality of life for patients with thalassemia than its predecessor, deferoxamine (Desferal, Novartis), because of its oral tablet form."3.79A pharmaco-economic evaluation of deferasirox for treating patients with iron overload caused by transfusion-dependent thalassemia in Taiwan. ( Chang, HH; Chung, KP; Ho, WL; Jou, ST; Lin, DT; Lin, KH; Lu, MY; Yang, SS; Yang, YL, 2013)
" The generic drugs deferiprone, deferoxamine and their combination offer a safer, less expensive and complete treatment of iron overload in thalassaemia and other iron loading conditions."3.79A record number of fatalities in many categories of patients treated with deferasirox: loopholes in regulatory and marketing procedures undermine patient safety and misguide public funds? ( Kontoghiorghes, GJ, 2013)
" The complete treatment of transfusional iron overload in thalassaemia using the deferiprone (L1) and deferoxamine combination is a paradigm to be followed in the treatment of many other metal toxicity conditions."3.79The proceedings of the 20th International Conference on Chelation held in the USA: advances on new and old chelation therapies. ( Kontoghiorghes, GJ, 2013)
"The Thalassemia Clinical Research Network collected adherence information from 79 patients on deferoxamine and 186 on deferasirox from 2007 to 2009."3.77Iron chelation adherence to deferoxamine and deferasirox in thalassemia. ( Coates, T; Giardina, PJ; Haines, D; Kwiatkowski, J; Mednick, L; Neufeld, EJ; Olivieri, N; Pakbaz, Z; Porter, J; Sobota, A; Thompson, AA; Trachtenberg, F; Vichinsky, E; Yamashita, R, 2011)
"In iron overload conditions, plasma contains non-transferrin bound iron species, collectively referred to as plasma NTBI."3.76Mechanisms for the shuttling of plasma non-transferrin-bound iron (NTBI) onto deferoxamine by deferiprone. ( Eccleston, J; Evans, P; Hider, RC; Kayyali, R; Porter, JB, 2010)
"Deferiprone (DFP) has been evaluated in a wide range of disorders, but most data come from transfusion-dependent thalassemia."3.76Deferiprone. ( Longo, F; Massano, D; Piga, A; Roggero, S; Salussolia, I; Serra, M, 2010)
"In this report we firstly describe a case of reactivation of hepatitis B virus (HBV) replication occurred in a patient affected by Thalassemia major which underwent a combined chelation therapy with desferioxamine (DFO) and deferiprone (DFP)."3.75Hepatitis B virus reactivation during combined therapy with deferiprone and desferioxamine in a hepatitis B surface antigen thalassemic carrier. ( Ammirabile, M; Cinque, P; Di Matola, T; Lanza Galeota, A; Prossomariti, L; Ricchi, P, 2009)
" The introduction of effective chelation therapy protocols using primarily deferiprone (L1) in combination with deferoxamine (DFO) resulted in the reduction of iron overload induced cardiac failures, which is the main cause of death in thalassemia major."3.75Advances in the prevention and treatment are changing thalassemia from a fatal to a chronic disease. experience from a Cyprus model and its use as a paradigm for future applications. ( Kolnagou, A; Kontoghiorghes, GJ, 2009)
" The known predisposing factors of infection include prior splenectomy, iron overload and use of iron chelator such as deferoxamine (DFO)."3.75Effects of chelators (deferoxamine, deferiprone and deferasirox) on the growth of Klebsiella pneumoniae and Aeromonas hydrophila isolated from transfusion-dependent thalassemia patients. ( Chan, GC; Chan, S; Ha, SY; Ho, PL, 2009)
"Non-transferrin-bound iron (NTBI) is detectable in plasma of beta-thalassemia patients with transfusional iron overload."3.74Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasma. ( Fucharoen, S; Phisalaphong, C; Porter, JB; Srichairatanakool, S; Thephinlap, C, 2007)
"Deferoxamine mesylate (DFO) reduces morbidity and mortality associated with transfusional iron overload."3.74Outcomes, utilization, and costs among thalassemia and sickle cell disease patients receiving deferoxamine therapy in the United States. ( Baladi, JF; Coates, TD; Delea, TE; Hagiwara, M; Phatak, PD; Thomas, SK, 2008)
"For the past 2-6 years, two groups of thalassemia patients, one of 16 patients on deferoxamine (DFO) monotherapy (35-80 mg/kg, 2-5 days/week) and the other group comprising 19 patients on a deferiprone (L1) and DFO combination therapy (L1 75-100 mg/kg/day and DFO 30-60 mg/kg, 1-5 days/week), have been studied and compared before and after the introduction of the combination therapy."3.74Long term comparative studies in thalassemia patients treated with deferoxamine or a deferoxamine/deferiprone combination. Identification of effective chelation therapy protocols. ( Economides, C; Eracleous, E; Kolnagou, A; Kontoghiorghes, GJ, 2008)
"The incidence of cardiomyopathy was monitored in a 6-year follow-up study involving 56 transfused thalassemia patients treated with deferoxamine (DFO), deferiprone (L1) or their combination."3.73Low serum ferritin levels are misleading for detecting cardiac iron overload and increase the risk of cardiomyopathy in thalassemia patients. The importance of cardiac iron overload monitoring using magnetic resonance imaging T2 and T2*. ( Economides, C; Eracleous, E; Kolnagou, A; Kontoghiorghes, GJ, 2006)
"In patients with thalassemia major (TM) who are non-compliant with long-term deferoxamine (DFO) chelation, survival is limited mainly because of cardiac complications of transfusional siderosis."3.72Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation. ( Berant, M; Hershko, C; Miskin, H; Tamary, H; Yaniv, I, 2003)
"We studied the changing pattern of the distribution of ferritin levels in 430 regularly-transfused patients with thalassemia in an attempt to evaluate compliance of chelation with deferoxamine."3.71Variations of ferritin levels over a period of 15 years as a compliance chelation index in thalassemic patients. ( Berdousi, H; Dinopoulos, A; Kattamis, A; Kattamis, C; Ladis, V, 2001)
"Compliance with parenteral administration of deferoxamine is often poor in thalassemic patients with iron overload."3.71Long-term administration of high-dose deferoxamine 2 days per week in thalassemic patients. ( Becker, A; Girot, R; Hagège, I; Kanfer, A; Kerdaffrec, T, 2001)
"A number of studies have shown that regular chelation therapy with deferoxamine is effective in patients with secondary hemochromatosis."3.69[Long-term efficacy of subcutaneous administration of deferoxamine in patients with secondary hemochromatosis]. ( Fujisawa, S; Kobayashi, M; Yano, K, 1996)
"We reviewed the linear growth and growth plate morphology in all children with homozygous beta thalassemia followed in Toronto, for whom monthly height percentiles were available before, and for a 36-month period after, the initiation of nightly subcutaneous deferoxamine therapy."3.68Growth failure and bony changes induced by deferoxamine. ( Bailey, JD; Freedman, MH; Harris, J; Khattak, S; Koren, G; Olivieri, NF; Reilly, BJ; Templeton, DM, 1992)
"The effect of the iron chelator deferoxamine (DFO) on resistance to infection with Listeria monocytogenes in mice with a condition analogous to human beta-thalassemia was studied."3.68Deferoxamine increases the susceptibility of beta-thalassemic, iron-overloaded mice to infection with Listeria monocytogenes. ( Ampel, NM; Bejarano, GC; Saavedra, M, 1992)
"Deferoxamine is still today the only preventive and curative treatment of transfusional hemochromatosis."3.68[Intensifying iron chelating therapy with desferrioxamine using implantable venous access catheters (Port-A-Cath)]. ( Clairicia, M; de Montalembert, M; Girot, R; Hannedouche, T; Jan, D; Sidi, D, 1992)
"To assess the effects of deferoxamine (DFO) on the kidneys, we studied 27 patients with thalassemia major on chronic subcutaneous (s."3.68The effects of subcutaneous deferoxamine administration on renal function in thalassemia major. ( Bentur, Y; Kochavi-Atiya, Y; Koren, G; Olivieri, NF, 1991)
" We describe a case of this unusual condition in a 17-year-old male patient with thalassemia intermedia requiring transfusion, who was also taking deferoxamine."3.68Yersinia enterocolitica infection with ileal perforation associated with iron overload and deferoxamine therapy. ( deSa, D; Gately, J; Mazzoleni, G; Riddell, RH, 1991)
"Metaphyseal irregularity and abnormal vertebral bodies resembling a bone dysplasia were seen in two of five children with thalassemia major who were begun on a regimen of hypertransfusion and chelation with deferoxamine before the age of 3 years."3.68Deferoxamine-induced bone dysplasia in patients with thalassemia major. ( Brill, PW; Cunningham-Rundles, S; Giardina, PJ; Winchester, P, 1991)
"To determine whether survival of patients with beta-thalassemia major has been prolonged by management that utilizes hypertransfusion and chelation with deferoxamine, we analyzed longevity by the Kaplan-Meier product-limit method."3.68Prolonged survival in patients with beta-thalassemia major treated with deferoxamine. ( Ehlers, KH; Engle, MA; Giardina, PJ; Hilgartner, MW; Lesser, ML, 1991)
"Daily subcutaneous infusion of deferoxamine in thalassemia and other transfusion dependent-patients can successfully treat iron overload, but most patients, mainly young children and teenagers may not comply with this method."3.68[Intravenous administration of deferoxamine in over-night hospitalization: efficacy and good psychological tolerance in thalassemic children]. ( Bachelot, C; Plantaz, D, 1990)
"The use of deferoxamine for iron chelation in transfusion-dependent thalassemia major is limited by serious neurotoxicity (hearing and vision loss)."3.68Comparison of deferoxamine pharmacokinetics between asymptomatic thalassemic children and those exhibiting severe neurotoxicity. ( Bentur, Y; Carley, H; Freedman, MH; Koren, G; Olivieri, N; Tesoro, A, 1990)
"Eight patients with transfusion-dependent thalassemia major were given continuous intravenous infusions of the chelator, deferoxamine mesylate, to reduce iron overload."3.68Pulmonary syndrome in patients with thalassemia major receiving intravenous deferoxamine infusions. ( Freedman, MH; Grisaru, D; MacLusky, I; Olivieri, N; Thorner, PS, 1990)
"Beginning chelation treatment with deferoxamine before the age of puberty can help children with transfusion-dependent thalassemia major to attain normal sexual maturation."3.68Effect of age at the start of iron chelation therapy on gonadal function in beta-thalassemia major. ( Andrews, DF; Bronspiegel-Weintrob, N; Freedman, MH; Holland, FJ; Olivieri, NF; Tyler, B, 1990)
"Sixteen patients (age range, 3 to 17 years) with transfusion-dependent beta-thalassemia major were studied prospectively, beginning at the onset of chelation therapy with deferoxamine (desferrioxamine)."3.67A prospective evaluation of iron chelation therapy in children with severe beta-thalassemia. A six-year study. ( Gonzalez-Crussi, F; Honig, GR; Ingrisano, C; Lloyd-Still, JD; Maurer, HS, 1988)
"Of 89 patients receiving nightly subcutaneous deferoxamine for transfusion-dependent thalassemia major or Diamond-Blackfan anemia, 13 presented with visual loss or deafness of acute onset or both."3.67Visual and auditory neurotoxicity in patients receiving subcutaneous deferoxamine infusions. ( Buncic, JR; Chew, E; Gallant, T; Harrison, RV; Keenan, N; Logan, W; Mitchell, D; Olivieri, NF; Ricci, G; Skarf, B, 1986)
"We examined the efficacy of long-term subcutaneous deferoxamine therapy in the prevention of iron-related cardiac disease in patients with thalassemia major who began treatment after the age of 10 years."3.67Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major. ( Colan, S; Freedman, MH; Nathan, DG; Olivieri, N; Propper, R; Rose, V; Sallan, D; Wolfe, L, 1985)
"We evaluated decreasing deferoxamine-induced urinary iron excretion during intensive chelation therapy in four children with thalassemia."3.66Response to long-term deferoxamine therapy in thalassemia. ( Cohen, A; Martin, M; Schwartz, E, 1981)
" Deferoxamine-induced urinary excretion of iron was considerably less than that reported in patients with thalassemia major who were receiving regular blood transfusions."3.66Iron burden in sickle cell anemia. ( O'Brien, RT, 1978)
"The iron-chelating agent, deferoxamine, was studied in 16 patients with thalassemia major."3.66Iron chelation therapy with deferoxamine in Cooley anemia. ( Cohen, A; Schwartz, E, 1978)
"Iron overload is the primary cause of mortality and morbidity in thalassemia major despite advances in chelation therapy."2.78Combined chelation therapy with deferasirox and deferoxamine in thalassemia. ( Evans, P; Harmatz, P; Kurio, G; Lal, A; Neumayr, L; Ng, V; Porter, J; Sweeters, N; Vichinsky, E, 2013)
" There was no significant difference in the proportion of patients with adverse events in the two therapy groups although the nature of the adverse events differed according to the chelation regimen."2.72A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemia. ( Fischer, R; Galanello, R; Kattamis, A; Ladis, V; Leoni, G; Lund, U; Piga, A; Tricta, F; Voi, V, 2006)
"The most frequent side effects were joint pain, stiffness or swelling in 6 patients (35."2.69Efficacy and side effects of deferiprone (L1) in thalassemia patients not compliant with desferrioxamine. ( Chamoun, FM; Khoriaty, AI; Koussa, S; Mourad, FH; Neeman, R; Saad, MA; Taher, A, 1999)
" During the course of the trial, several possible adverse effects have been encountered."2.67Efficacy and possible adverse effects of the oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one (L1) in thalassemia major. ( al-Refaie, FN; Hoffbrand, AV; Kontoghiorghes, GJ; Nortey, P; Wickens, DG; Wonke, B, 1992)
" Selected protocols using DFO, L1, and their combination can be designed for personalized chelation therapy in TI, which can effectively and safely remove all the excess toxic iron and prevent cardiac, liver, and other organ damage."2.53Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. ( Kontoghiorghe, CN; Kontoghiorghes, GJ, 2016)
"Thalassemia is a chronic inherited blood disorder that reduces hemoglobin production, causing chronic hemolytic anemia."2.53Clinical Management of Patients With Thalassemia Syndromes. ( Haines, D; Martin, M, 2016)
"Iron overload has many different causes, both genetic and environmental."2.48Iron mobilization using chelation and phlebotomy. ( Aaseth, J; Andersen, O; Flaten, TP; Kontoghiorghes, GJ, 2012)
"Thalassemia is an autosomal recessive disorder associated with defective synthesis of the α- or β-chain of hemoglobin."2.48Hematopoietic stem cell transplantation for thalassemia. ( Elborai, Y; Lehmann, L; Uwumugambi, A, 2012)
"Iron overload is a major cause of morbidity and mortality in transfusion-dependent anemias."2.46An update on disordered iron metabolism and iron overload. ( Ward, R, 2010)
"Monitoring of iron overload has advanced with the increasing use of MRI techniques to estimate iron balance (changes in liver iron concentration) and extrahepatic iron distribution (myocardial T2*)."2.46Iron overload in thalassemia and related conditions: therapeutic goals and assessment of response to chelation therapies. ( Porter, JB; Shah, FT, 2010)
"Thalassemia is anemia of variable severity, arising from mutations of genes encoding the hemoglobin alpha and beta chains."2.44Mechanisms of and obstacles to iron cardiomyopathy in thalassemia. ( Chang, JS; Lin, HS; Peng, CT; Tsai, CH; Wu, KH, 2008)
"Deferiprone is a three-times-daily oral iron chelator, but has limited availability in the United States."2.44Consequences and costs of noncompliance with iron chelation therapy in patients with transfusion-dependent thalassemia: a literature review. ( Baladi, JF; Coates, TD; Delea, TE; Edelsberg, J; Phatak, PD; Sofrygin, O; Thomas, SK, 2007)
" Increasing DFO dosing does not increase NTBI removal, but instead leads to a greater rebound in NTBI on cessation of intravenous infusion."2.43Recent insights into interactions of deferoxamine with cellular and plasma iron pools: Implications for clinical use. ( Davis, BA; Evans, P; Hair, T; Porter, JB; Rafique, R; Shah, FT; Srichairatanakool, S, 2005)
"If untreated, iron overload is responsible for heart, liver and endocrine diseases."2.42Pharmacotherapy of iron overload in thalassaemic patients. ( Ceci, A; De Mattia, D; De Sanctis, V; Felisi, M, 2003)
" This substance is well absorbed orally and has been shown to enhance the excretion of ferric ion in iron loaded rats."2.36[Iron chelation. Biological significance and medical application]. ( Peter, HH, 1983)
"Hemochromatosis is a syndrome which, when fully expressed, is manifested by melanoderma , diabetes mellitus, and liver cirrhosis, with iron overload involving parenchymal and reticuloendothelial cells in many organ systems."2.36Iron overload disorders: natural history, pathogenesis, diagnosis, and therapy. ( Kellermeyer, RW; McLaren, GD; Muir, WA, 1983)
" In the United States, deferiprone has been approved for three times daily dosing since 2011 and has recently gained approval for twice-daily administration."1.91An evaluation of deferiprone as twice-a-day tablets or in combination therapy for the treatment of transfusional iron overload in thalassemia syndromes. ( Badawy, SM; Shah, A; Shah, R, 2023)
"Iron overload is a major complication of transfusion-dependent thalassemia (TDT) and requires iron chelation (IC) therapy."1.62Using of deferasirox and deferoxamine in refractory iron overload thalassemia. ( Buaboonnam, J; Narkbunnam, N; Phuakpet, K; Pongtanakul, B; Sanpakit, K; Takpradit, C; Vathana, N; Viprakasit, V, 2021)
"Reversal of arrhythmia to sinus rhythm was noted in all patients."1.56Combined chelation with high-dose deferiprone and deferoxamine to improve survival and restore cardiac function effectively in patients with transfusion-dependent thalassemia presenting severe cardiac complications. ( Chao, YH; Chuang, TY; Li, JP; Weng, TF; Wu, KH, 2020)
"Iron overload was assessed by the T2* technique."1.48The effect of desferrioxamine chelation versus no therapy in patients with non transfusion-dependent thalassaemia: a multicenter prospective comparison from the MIOT network. ( Allò, M; Campisi, S; Gamberini, MR; Lisi, R; Mangione, M; Meloni, A; Missere, M; Peluso, A; Pepe, A; Pistoia, L; Positano, V; Renne, S; Ricchi, P; Spasiano, A; Spiga, A, 2018)
"Cardiac iron overload was induced to a greater extent than in a previous study by feeding the mice with an iron-enriched diet for 4 months."1.43Dual T-type and L-type calcium channel blocker exerts beneficial effects in attenuating cardiovascular dysfunction in iron-overloaded thalassaemic mice. ( Chattipakorn, N; Chattipakorn, SC; Fucharoen, S; Kumfu, S, 2016)
"Thalassemia is a congenital blood disorder requiring chronic blood transfusions and daily iron chelation therapy."1.38Beliefs about chelation among thalassemia patients. ( Grady, R; Haines, D; Horne, R; Kwiatkowski, JL; Mednick, L; Neufeld, EJ; Olivieri, N; Pakbaz, Z; Quinn, CT; Sobota, A; Thompson, AA; Trachtenberg, FL; Yamashita, R, 2012)
"Thalassemia is a chronic hereditary disease in which patients with severe disease present with anemia during their first year of life."1.37Health-related quality of life in Thai thalassemic children treated with iron chelation. ( Pankaew, T; Torcharus, K, 2011)
"Dental caries were significantly higher in thalassemics."1.33Physical growth patterns and dental caries in thalassemia. ( Dewan, P; Gomber, S, 2006)
"Body disproportion and severe degree of osteopenia (BMD SDSBA -2."1.31Persistence of delayed adrenarche in boys with thalassemia. ( De Martinis, F; De Terlizzi, F; Di Maio, S; Esposito, G; Filosa, A, 2001)
"6 patients who developed liver cirrhosis before or after their thalassemia was cured by bone marrow transplantation (age at transplantation, 11 to 25 years)."1.31Reversibility of cirrhosis in patients cured of thalassemia by bone marrow transplantation. ( Angelucci, E; Lucarelli, G; Muretto, P, 2002)
" The results show that L1 is less toxic than DF to normal bone marrow myeloid progenitors (ID50:130 mumol/l versus 7."1.29Differential toxicity of alpha-keto hydroxypyridine iron chelators and desferrioxamine to human haemopoietic precursors in vitro. ( al-Refaie, FN; Cunningham, JM; Hoffbrand, AV; Hunter, AE; Sheppard, LN, 1994)
"To determine the frequency of eye and auditory complications and their relationship to drug dosage and iron stores in patients receiving deferoxamine, we studied 52 regularly transfused patients who received deferoxamine by subcutaneous or intravenous infusion in doses from 26 to 136 mg/kg/day, and whose serum ferritin levels of 185 to 17,775 micrograms/L reflected a wide range of iron stores."1.28Vision and hearing during deferoxamine therapy. ( Cohen, A; Konkle, DF; Martin, M; Mizanin, J; Schwartz, E, 1990)
"Forty-seven patients with thalassaemia have been studied to define risk factors for development of sensorineural hearing loss, and to establish guidelines for safe chelation."1.28Desferrioxamine ototoxicity: evaluation of risk factors in thalassaemic patients and guidelines for safe dosage. ( East, CA; Hazell, JW; Huehns, ER; Jaswon, MS; Porter, JB, 1989)
" The dosage and the route of administration (IV, IM, SC) were adapted to the amount of iron transfused and to the nature of the disease."1.28[Treatment of post-transfusion iron overload by deferoxamine]. ( de Montalembert, M; Girot, R; Hannedouche, T; Llados, A, 1989)
"Successful pregnancy is described in a patient with beta-thalassaemia major, transfusion-dependent from four months of age and treated with desferrioxamine from 13 years of age."1.27Successful pregnancy in beta-thalassaemia major. ( Martin, K, 1983)
" The incidence of such changes is not related to drug dosage or to ferritin level but to abnormality of the extended glucose tolerance test."1.27Ocular changes in patients undergoing long-term desferrioxamine treatment. ( Arden, GB; Huehns, ER; Kennedy, C; Wonke, B, 1984)
"Among our patients, conductive hearing loss was not more frequent than in patients without beta thalassemia."1.27Hearing loss and desferrioxamine in homozygous beta-thalassemia. ( Albera, R; Bianco, L; Gabutti, V; Lacilla, M; Morra, B; Pia, F; Piga, A, 1988)
" However, the desferrioxamine dosage was similar in both our groups (less than 60 mg/kg a day), and lower in the affected group than other authors have reported."1.27Hearing loss attributed to desferrioxamine in patients with beta-thalassaemia major. ( Barratt, PS; Toogood, IR, 1987)
"The liver iron content of patients with liver cirrhosis was within the normal range."1.27Comparison between serum ferritin and computed tomographic densities of liver, spleen, kidney and pancreas in beta-thalassaemia major. ( Babiker, MA; Hafeez, MH; Karrar, ZA; Patel, PJ, 1987)
" Since dose-response curves were highly variable the treatment schedule should be tailored to the individual needs of each patient."1.26Iron chelation in transfusion-dependent thalassemia with chronic hepatitis. ( Cao, A; Cornacchia, G; Cossu, P; De Virgiliis, S; Frau, F; Lobrano, R; Loi, A; Loi, E; Nucaro, A; Sanna, G; Toccafondi, C, 1982)
"Since patients with thalassemia are not growth hormone deficient, the data suggest the possibility of defective hepatic biosynthesis of somatomedin."1.26Depressed serum somatomedin activity in beta-thalassemia. ( Graziano, JH; Hilgartner, MW; Levine, LS; Markenson, AL; New, MI; Saenger, P; Schwartz, E, 1980)
"Deferoxamine was given intravenously for 12 months and subcutaneously in the next 18 months."1.26[Role and therapeutic use of deferoxamine in iron overload due to thalassemia (author's transl)]. ( Bachelot, C; Bost, M; Joannard, A; Lévy, G, 1980)

Research

Studies (488)

TimeframeStudies, this research(%)All Research%
pre-1990288 (59.02)18.7374
1990's71 (14.55)18.2507
2000's65 (13.32)29.6817
2010's54 (11.07)24.3611
2020's10 (2.05)2.80

Authors

AuthorsStudies
Kwiatkowski, JL3
Hamdy, M2
El-Beshlawy, A2
Ebeid, FSE1
Badr, M1
Alshehri, A1
Kanter, J1
Inusa, B1
Adly, AAM1
Williams, S2
Kilinc, Y1
Lee, D1
Tricta, F3
Elalfy, MS1
Kolnagou, A12
Kleanthous, M3
Kontoghiorghes, GJ23
Rosin, B1
Sahel, JA1
Shah, R1
Shah, A1
Badawy, SM1
Geneen, LJ1
Dorée, C4
Estcourt, LJ1
Chuang, TY1
Li, JP1
Weng, TF1
Wu, KH3
Chao, YH1
Takpradit, C1
Viprakasit, V3
Narkbunnam, N1
Vathana, N1
Phuakpet, K1
Pongtanakul, B1
Sanpakit, K1
Buaboonnam, J1
Shafie, AA1
Wong, JHY1
Ibrahim, HM1
Mohammed, NS1
Chhabra, IK1
Zardkhoni, SZ1
Moghaddam, AG1
Rad, F1
Ghatee, MA1
Omidifar, N1
Ghaedi, M1
Etemadfar, P1
Hadjidemetriou, M1
Bollig, C1
Schell, LK1
Rücker, G2
Allert, R1
Motschall, E2
Niemeyer, CM2
Bassler, D2
Meerpohl, JJ2
Sridharan, K1
Sivaramakrishnan, G1
Ricchi, P2
Meloni, A1
Pistoia, L1
Spasiano, A1
Spiga, A1
Allò, M1
Gamberini, MR2
Lisi, R1
Campisi, S2
Peluso, A1
Missere, M1
Renne, S1
Mangione, M1
Positano, V1
Pepe, A3
Wahidiyat, PA1
Yosia, M1
Sari, TT1
Georgakopoulos, CD1
Tsapardoni, F1
Kostopoulou, EV1
Makri, OE1
Taher, AT2
Origa, R1
Perrotta, S1
Kouraklis, A1
Ruffo, GB1
Kattamis, A5
Goh, AS1
Huang, V1
Zia, A1
Herranz, RM1
Porter, JB9
Hider, RC2
Hoffbrand, AV17
Dou, H1
Qin, Y1
Chen, G1
Zhao, Y1
Ho, WL1
Chung, KP1
Yang, SS1
Lu, MY1
Jou, ST1
Chang, HH1
Yang, YL1
Lin, DT1
Lin, KH1
Olivieri, NF10
Brittenham, GM2
Fisher, SA2
Brunskill, SJ3
Gooding, S2
Chowdhury, O2
Roberts, DJ4
Xia, S1
Zhang, W1
Huang, L1
Jiang, H1
Al-Kloub, MI1
Salameh, TN1
Froelicher, ES1
Wu, CH1
Yang, CP1
Lai, CC1
Wu, WC1
Chen, YH1
Tanphaichitr, A1
Kusuwan, T1
Limviriyakul, S1
Atipas, S1
Pooliam, J1
Sangpraypan, T1
Tanphaichitr, VS1
Karimi, M1
Haghpanah, S1
Adly, AA1
Ebeid, FS1
Teawtrakul, N1
Jetsrisuparb, A2
Sirijerachai, C1
Chansung, K1
Wanitpongpun, C1
Kumfu, S2
Chattipakorn, SC2
Fucharoen, S4
Chattipakorn, N2
Conte, R1
Ruggieri, L1
Gambino, A1
Bartoloni, F1
Baiardi, P1
Bonifazi, D1
Bonifazi, F1
Felisi, M2
Giannuzzi, V1
Padula, R1
Putti, MC1
Del Vecchio, GC2
Maggio, A3
Filosa, A3
Iacono, A1
Mangiarini, L1
Ceci, A2
Kontoghiorghe, CN1
Yadav, SP1
Martin, M5
Haines, D3
El-Shazly, AA1
Ebeid, WM1
Elkitkat, RS1
Deghedy, MR1
Cappellini, MD2
Furlan, L1
Graziadei, G1
Colombo, G1
Forzenigo, LV1
Solbiati, M1
Peng, CT2
Chang, JS1
Tsai, CH2
Lin, HS1
Cinque, P1
Lanza Galeota, A1
Di Matola, T1
Ammirabile, M1
Prossomariti, L2
Vitrano, A1
Capra, M2
Cuccia, L2
Gagliardotto, F1
Romeo, MA4
Magnano, C1
Caruso, V1
Argento, C1
Gerardi, C1
Violi, P1
Malizia, R1
Cianciulli, P1
Rizzo, M1
D'Ascola, DG1
Quota, A1
Fidone, C1
Rigano, P2
D'Amico, G2
Morabito, A2
Gluud, C1
Dahlui, M1
Hishamshah, MI1
Rahman, AJ1
Aljunid, SM1
Yazman, D1
Economides, C4
Eracleous, E4
Chan, GC2
Chan, S1
Ho, PL1
Ha, SY2
Efstathiou, A1
Michaelides, Y2
Berdoukas, V3
Carson, S1
Nord, A1
Dongelyan, A1
Gavin, S1
Hofstra, TC1
Wood, JC2
Coates, T3
Komvilaisak, P1
Wiangnon, S1
Jetsrisuparb, C1
Fragatou, S1
Tsourveloudis, I1
Manesis, G1
Evans, P3
Kayyali, R1
Eccleston, J1
Hershko, C12
Piga, A12
Roggero, S3
Salussolia, I1
Massano, D1
Serra, M1
Longo, F3
Terpos, E1
Voskaridou, E1
Ward, R1
Shah, FT2
Farmaki, K1
Lee, WS1
Toh, TH1
Chai, PF1
Soo, TL1
Trachtenberg, F1
Vichinsky, E2
Pakbaz, Z2
Mednick, L2
Sobota, A2
Kwiatkowski, J1
Thompson, AA2
Porter, J2
Giardina, PJ8
Olivieri, N5
Yamashita, R2
Neufeld, EJ2
Mavrogeni, S1
Torcharus, K1
Pankaew, T1
Antes, G1
Fleeman, N1
Flaten, TP1
Aaseth, J1
Andersen, O1
Gaur, A1
Elborai, Y1
Uwumugambi, A1
Lehmann, L1
Lal, A1
Sweeters, N1
Ng, V1
Neumayr, L1
Kurio, G1
Harmatz, P2
Trachtenberg, FL1
Quinn, CT1
Grady, R1
Horne, R1
Davis, BA2
Miskin, H1
Yaniv, I1
Berant, M1
Tamary, H1
Bansal, V1
Elgarbly, I1
Ghanchi, FD1
Atkinson, PL1
Neocleous, K1
REWALD, EF1
WOEHLER, F2
RAY, RN1
CHATTERJEA, JB1
GHOSH, SK1
CARLOS, AG1
SOARES, AD1
SCOVILLE, B1
BORCHERS, HG1
SCHAUER, A1
REWALD, E1
SCURO, LA1
BROCCIA, G1
DOBRILLA, G1
TAGLIAMONTE, A1
ROMANO, C1
MASSIMO, L1
TORTOROLO, G1
STEINER, M1
BALDINI, M1
DAMESHEK, W1
ERLANDSON, ME1
GOLUBOW, J1
WEHMAN, J1
SMITH, CH1
SMITH, RS1
MOESCHLIN, S1
SCHNIDER, U1
RITTER, M1
CHANTRAINE, JM1
NEIMANN, N1
PIERSON, M1
MANCIAUX, M1
VERT, P1
SCHAACK, JC1
De Sanctis, V7
De Mattia, D2
Di Stefano, M1
Chiabotto, P1
Roggia, C1
Garofalo, F1
Lala, R1
Isaia, GC1
Gomber, S2
Saxena, R1
Madan, N1
Sodani, P2
Gaziev, D3
Polchi, P5
Erer, B3
Giardini, C4
Angelucci, E5
Baronciani, D4
Andreani, M2
Manna, M1
Nesci, S1
Lucarelli, B1
Clift, RA1
Lucarelli, G7
D'Angelo, E1
Mirra, N1
Rocca, A1
Carnelli, V1
Ng, DM1
Fong, DY1
Lau, YL1
Borgna-Pignatti, C4
Rugolotto, S1
De Stefano, P4
Zhao, H1
Forni, GL1
Ghilardi, R1
Cnaan, A1
Anderson, LJ1
Westwood, MA1
Holden, S1
Davis, B1
Prescott, E1
Wonke, B14
Walker, JM1
Pennell, DJ2
Marletto, F1
Sacchetti, L3
Rees, D1
Howard, J2
Hyde, C1
Alderson, P1
Brunskill, S1
Link, G5
Konijn, AM2
Cabantchik, ZI1
Rafique, R1
Srichairatanakool, S2
Hair, T1
Vinciguerra, T1
Gallo, V1
Gaziev, J1
Telfer, P2
Constantinidou, G1
Andreou, P1
Christou, S2
Modell, B9
Angastiniotis, M2
Fischer, R2
Nielsen, P1
Mudiyanse, RM1
Coen, PG1
Hadjigavriel, M1
Kolnakou, A1
Pangalou, E1
Pavlides, N2
Psiloines, M1
Simamonian, K1
Skordos, G1
Sitarou, M1
Galanello, R1
Leoni, G1
Ladis, V2
Voi, V1
Lund, U1
Dewan, P1
Hyde, CJ1
Payne, KA1
Desrosiers, MP1
Caro, JJ1
Baladi, JF3
Lordan, N1
Proskorovsky, I1
Ishak, K1
Rofail, D1
Delea, TE2
Edelsberg, J1
Sofrygin, O1
Thomas, SK2
Phatak, PD2
Coates, TD2
Thephinlap, C1
Phisalaphong, C1
Hagiwara, M1
Kidson-Gerber, GL1
Francis, S1
Lindeman, R1
Kontos, C1
Kyriacou, K1
Manz, C1
Naja, M1
Eltagui, M1
Tarabishi, C1
Youssry, I1
Sobh, H1
Sharaf, I1
Mostafa, A1
Shaker, O1
Taher, A2
Carcassi, U1
Bannerman, RM1
Keusch, G1
Kreimer-Birnbaum, M1
Vance, VK1
Vaughan, S1
Wöhler, F1
Gyftaki, H1
Kesse-Elias, M1
Constantoulakis, M2
Malamos, B1
Cohen, A11
Witzleben, C1
Schwartz, E12
Callender, ST8
Weatherall, DJ9
Kattamis, C3
Fitsialos, J1
Sinopoulou, C1
Smith, GN1
Davies, SC3
Marcus, RE3
Hungerford, JL1
Miller, MH1
Arden, GB2
Huehns, ER6
Bousquet, J1
Navarro, M1
Robert, G1
Aye, P1
Michel, FB1
Robins-Browne, RM1
Prpic, JK1
Gordts, B1
Rummens, E1
deMeirleir, L1
Butzler, JP1
Bantock, HM1
Underwood, SR1
Walton, S1
Broglia, AM1
Scharnetzky, M1
König, R4
Lakomek, M1
Tillmann, W7
Schröter, W8
Triadou, P3
Girot, R11
Lapoumeroulie, C1
Pomarede, R2
Constant, S2
Nienhuis, AW6
Anagnou, NP1
Ley, TJ1
Peter, HH1
Engle, MA3
Ehlers, KH4
O'Loughlin, JE1
Hilgartner, MW7
Propper, R2
Nathan, D2
North, ML1
Lang, JM1
Bergerat, JP1
Giron, C1
Oberling, F1
Mayer, S1
McLaren, GD1
Muir, WA1
Kellermeyer, RW1
Beck, W1
Roeser, HP1
Martin, K1
Bianco, I4
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Clinical Trials (14)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
The Efficacy and Safety of Ferriprox® for the Treatment of Transfusional Iron Overload in Patients With Sickle Cell Disease or Other Anemias[NCT02041299]Phase 4230 participants (Actual)Interventional2014-04-17Terminated (stopped due to Difficulties with additional recruitment as pool of potential patients was exhausted, and sufficient information for determination of study outcome measure was already obtained)
Quality of Life and Treatment Satisfaction in β-Thalassemia Patients Receiving Deferasirox[NCT03358498]75 participants (Anticipated)Observational2017-12-01Not yet recruiting
A Randomized, Open-label, Multicenter, Two Arm, Phase II Study to Investigate the Benefits of an Improved Deferasirox Formulation (Film-coated Tablet)[NCT02125877]Phase 2173 participants (Actual)Interventional2014-07-08Completed
Phase IV Study of the Use of Sequential DFP-DFO Versus DFP in Thalassemia Major Patients[NCT00733811]Phase 4213 participants (Actual)Interventional2000-09-30Completed
Safety of Deferasirox (ICL670) and Deferoxamine (Desferal or DFO) Combined Chelation Therapy in Patients With Transfusion Dependent Thalassemia and Iron Overload[NCT00901199]Phase 222 participants (Actual)Interventional2007-09-30Completed
A Longitudinal Cohort Study of Patients With Thalassemia in the Thalassemia Clinical Research Network[NCT00661804]416 participants (Actual)Observational2007-05-31Completed
Iron-mediated Vascular Disease in Sickle Cell Disease.[NCT01239901]150 participants (Actual)Observational2009-12-31Completed
Randomized Open-label Phase III Study With Deferiprone and/or Desferrioxamine in Iron Overloaded Patients[NCT00350662]Phase 395 participants (Actual)Interventional2002-01-31Completed
A Pilot Study of 5-Azacytidine and Oral Sodium Phenylbutyrate in Severe Thalassemia[NCT00005934]Phase 224 participants Interventional2000-06-30Completed
Effect of Hydroxyurea on the Level of Ineffective Erythropoiesis, Transfusion Requirement, and Fetal Hemoglobin Synthesis in Patients With Beta-Thalassemia-Intermedia[NCT00001958]Phase 2100 participants Interventional1999-12-31Completed
[NCT00000595]Phase 20 participants Interventional1978-01-31Completed
The Effect of Treatment With the Oral Iron Chelator Deferiprone on the Oxidative Stress of Blood Cells and on Iron Overload Status in Transfusion Dependent, Iron-overloaded Patients With Low Risk Myelodysplastic Syndrome[NCT02477631]Phase 219 participants (Actual)Interventional2016-02-29Completed
Double-blind, Randomized, Placebo Controlled, Dose-finding Phase 2 Clinical Trial of Intravenous Deferoxamine in Patients With Acute Ischemic Stroke Treated With Tissue Plasminogen Activator[NCT00777140]Phase 262 participants (Actual)Interventional2008-09-30Completed
Safety & Efficacy of Thalidomide in Children With Transfusion Dependent Thalassemia: a Quasi Randomized Control Trial in a Tertiary Care Hospital in Bangladesh[NCT06098014]Phase 360 participants (Anticipated)Interventional2023-03-08Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change From Baseline in Cardiac Iron

Cardiac iron is measured by MRI in milliseconds (ms). A score of less than 20 ms is indicative of cardiac iron overload. (NCT02041299)
Timeframe: Change from baseline to Week 52

Interventionmilliseconds (Least Squares Mean)
Deferiprone-0.022068
Deferoxamine-0.021773

Change From Baseline in Liver Iron Concentration (LIC)

LIC was measured by MRI. A score >7 mg/g dw is indicative of iron overload. (NCT02041299)
Timeframe: Change from baseline to Week 52

Interventionmg of iron per gram of liver dry weight (Least Squares Mean)
Deferiprone-4.13
Deferoxamine-4.38

Change From Baseline in Serum Ferritin

Serum ferritin provides a measure of iron level in the blood. Normal levels of serum ferritin are under 300 µg/L for females and 400 µg/L for males. (NCT02041299)
Timeframe: Change from baseline to Week 52

Interventionmicrograms per liter (Least Squares Mean)
Deferiprone-385.83
Deferoxamine-760.89

Change in Patient-reported Quality of Life, as Measured by the Short Form Health Survey (SF-36) or the Child Health Questionnaire (CHQ-PF50).

Adult patients completed the SF-36 questionnaire and minors completed the CHQ-PF50. These questionnaires yield a profile of functional health and well-being, based on 8 scales of physical and mental health measures: Physical Functioning, Role Limitations due to Physical Health, Bodily Pain, General Health Perceptions, Vitality, Social Functioning, Role Limitations due to Emotional Problems, and Mental Health (MH), and summary scores are produced for physical well-being and mental well-being. The summaries are scored from 0-100, with higher scores reflecting better outcomes. (NCT02041299)
Timeframe: Change from baseline to Week 52

,
Interventionscore on a scale (Mean)
SF-36 Physical SummarySF-36 Mental SummaryCHQ-PF50 Physical SummaryCHQ-PF50 Psychosocial Summary
Deferiprone43.144.729.342.5
Deferoxamine43.040.930.541.3

Area Under the Plasma Concentration-time Curve From Time Zero to the Last Quantifiable Concentration (AUClast)

Blood samples were collected to assess AUClast. (NCT02125877)
Timeframe: week 1, day 1: pre-dose (0 hour) and 1, 2, 3, 4, 8 and 24 hours post dose; week 3, day 1: pre-dose (0 hour) and 1, 2, 3, 4, 8 and 24 hours post dose

,
Interventionumol/L*h (Mean)
week1 (n=14,15)week 3 (n=13,15)
Deferasirox Dispersible Tablet (DFX-DT)11101590
Deferasirox Film-coated Tablet (DFX-FCT)10402110

Dererasirox Plasma Concentration

Blood samples were collected to assess deferasirox concentration. Dose-adjusted calculations are presented: (concentration/actual dose)*20 for participants on DFX-DT and (concentration/actual dose)*14 for participants on DFX-FCT. (NCT02125877)
Timeframe: Week 3, day 1, pre-dose (0 hour (h)) and 2 h post-dose; week 13, day 1, pre-dose (0 hour (h)) and 2 h post-dose; and week 21, day 1, pre-dose (0 hour (h)) and 2 h post-dose

,
Interventionumol/L (Mean)
week 3, pre-dose (n=63,70)week 3, 2 hours post-dose (n=67,76)week 13, pre-dose (n=69.56)week 13, 2 hours post-dose (n=74,59)week 21, pre-dose (n=54,59)week 21, 2 hours post-dose (n=59,64)
Deferasirox Dispersible Tablet (DFX-DT)39.680.837.178.746.689.8
Deferasirox Film-coated Tablet (DFX-FCT)27.395.531.392.543.1105

Frequency of Selected Gastro-intestinal (GI) Adverse Events

The percentage of participants with any GI adverse event, diarrhea, constipation, nausea, vomiting, abdominal pain was assessed. (NCT02125877)
Timeframe: 28 weeks

,
InterventionPercentage of participants (Number)
Any GI adverse eventAbdominal painConstipationDiarrheaNauseaVomiting
Deferasirox Dispersible Tablet (DFX-DT)61.626.715.134.926.722.1
Deferasirox Film-coated Tablet (DFX-FCT)58.626.48.033.327.617.2

Mean Domain Scores of the Modified Satisfaction With Iron Chelation Therapy (Modified SICT)

The modified SICT consisted of 13 items that represent 3 domains: adherence, satisfaction and concerns. The adherence domain consisted of 7 items, 6 which were measured using a 5-point response scale and was calculated by summing the 6 items. The score range from 6 to 30 and higher scores indicated worse adherence. The satisfaction domain consisted of 3 items, 2 which were measured using a 5-point response scale and was calculated by summing the 2 items. The score range from 2 to 10 and higher scores indicated worse satisfaction. The concerns domain consisted of 3 items to address any concerns or worries with his/her medication. All 3 items were measured on a 5-point response scale and were calculated by summing the 3 items. The score range from 3 to 15 and higher scores indicated fewer concerns. For all three domains, the meaningful difference between two treatment arms was determined to be 1 point. (NCT02125877)
Timeframe: weeks 2, 3, 13 and 24 (end of treatment or within 7 days of last dose)

,
Interventionscore on a scale (Mean)
week 2, adherence (n=70,70)week 2, satisfaction/preference (n=70,70)week 2, concerns (n=70,70)week 3, adherence (n=58,51)week 3, satisfaction/preference (n=58,51)week 3, concerns (n=58,51)week 13, adherence (n=59,64)week 13, satisfaction/preference (n=59,64)week 13, concerns (n=59,64)week 24, adherence (n=63,60)week 24, satisfaction/preference (n=63,60)week 24, concerns (n=63,60)
Deferasirox Dispersible Tablet (DFX-DT)10.35.212.910.95.412.411.25.412.712.55.811.8
Deferasirox Film-coated Tablet (DFX-FCT)7.62.813.87.72.614.07.82.913.67.52.913.7

Number of Participants With Weekly Average Compliance of Medication Consumption

A compliance questionnaire assessed whether the medication was taken. Weekly average compliance was calculated when there were at least four non-missing daily responses. (NCT02125877)
Timeframe: Weeks 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24

,
InterventionParticipants (Number)
week 1week 2week 3week 4week 5week 6week 7week 8week 9week 10week 11week 12week 13week 14week 15week 16week 17week 18week 19week 20week 21week 22week 23week 24
Deferasirox Dispersible Tablet (DFX-DT)566462585662555653525050495148484343404039383630
Deferasirox Film-coated Tablet (DFX-FCT)536456585851484645464241474242403938373636343324

Observed Maximum Plasma Concentration Following Drug Administration (Cmax)

Blood samples were collected to assess Cmax. (NCT02125877)
Timeframe: week 1, day 1: pre-dose (0 hour) and 1, 2, 3, 4, 8 and 24 hours post dose; week 3, day 1: pre-dose (0 hour) and 1, 2, 3, 4, 8 and 24 hours post dose

,
Interventionumol/L (Mean)
week 1 (n=14,15)week 3 (n=14,15)
Deferasirox Dispersible Tablet (DFX-DT)74.6118
Deferasirox Film-coated Tablet (DFX-FCT)79.3139

Overall Safety as Measured by Changes in Laboratory Values From Baseline

The percentage of participants with post-baseline laboratory values meeting specified criteria for notable/extended range was assessed. The following laboratory parameters were measured: platelet count, absolute neutrophils, serum creatinine , creatinine clearance, urinary protein/urinary creatinine ratio, alanine aminotransferase (ALT) and aspartate aminotransferase (AST). Note that within data categories, creat = creatinine, cons = consecutive, ULN = upper limit of normal and urin = urinary. (NCT02125877)
Timeframe: baseline (BL), 30 weeks

,
InterventionPercentage of participants (Number)
platelet count, notable range: <100 x 10^9/Lplatelet count, extended range: <50 x 10^9/Labsolute neutrophils, notable range: <1.5 x 10^9/Labsolute neut., extended range: <0.5 x 10^9/Lserum creat, 2 cons >33% incr. from BL and >ULNcreat clearance, notable range: 2 cons <60mL/mincreat clearance, extended range: 2 cons <40mL/minurin protein/urin creat ratio, 2 cons >1.0 mg/mgALT, notable range: >5 x ULN and >2 x BLALT, extended range: >10 x ULN and >2 x BLAST, notable range: >5 x ULN and >2 x BLAST, extended range: >10 x ULN and >2 x BL
Deferasirox Dispersible Tablet (DFX-DT)9.33.58.14.74.77.02.32.31.21.201.2
Deferasirox Film-coated Tablet (DFX-FCT)8.05.713.803.42.32.301.101.10

Overall Safety as Measured by Frequency of Adverse Events

The percentage of participants with adverse events, serious adverse events and deaths was assessed. (NCT02125877)
Timeframe: 28 weeks

,
InterventionPercentage of participants (Number)
Adverse eventsSAEsDeaths
Deferasirox Dispersible Tablet (DFX-DT)89.515.10
Deferasirox Film-coated Tablet (DFX-FCT)89.718.41.1

Palatability Questionnaire Score

"The palatability questionnaire consisted of 4 items. The first item measured the taste and aftertaste of the medication and were scored a on a 5-point response scale. The second item offered an additional response option of no aftertaste. The last 2 items referred to whether the medication was taken, i.e. swallowed or vomited, and how the participant perceived the amount of medication to be taken. The palatability summary score was calculated using a scoring matrix from items 1, 3 and 4 scores and the score ranges from 0 - 11. Higher scores indicated the best palatability. A meaningful difference between two treatment arms was determined to be 1 point." (NCT02125877)
Timeframe: weeks 2, 3, 13 and 24 (end of treatment or within 7 days of last dose)

,
Interventionscore on a scale (Mean)
week 2 (n=69,70)week 3 (n=57,51)week 13 (n=59,62)week 24 (n=63,60)
Deferasirox Dispersible Tablet (DFX-DT)9.08.89.38.8
Deferasirox Film-coated Tablet (DFX-FCT)10.810.810.810.9

Time to Reach the Maximum Plasma Concentration After Drug Administration (Tmax)

Blood samples were collected to assess Tmax. (NCT02125877)
Timeframe: week 1, day 1: pre-dose (0 hour) and 1, 2, 3, 4, 8 and 24 hours post dose; week 3, day 1: pre-dose (0 hour) and 1, 2, 3, 4, 8 and 24 hours post dose

,
Interventionhour (Median)
week 1 (n=14,15)week 3 (n=14,15)
Deferasirox Dispersible Tablet (DFX-DT)3.572.85
Deferasirox Film-coated Tablet (DFX-FCT)2.002.02

Weekly Average of Daily Scores of the Gastrointestinal (GI) Symptom Diary

The GI symptom diary consisted of 6 items, five which were scored using a 0 - 10 rating scale with item appropriate anchors to rate the symptom, for example, Pain in your belly: 0 = no pain and 10 = worst pain. The GI diary summary score was created using the 10 point response scale for the 5 items. The GI symptom daily diary had a minimum score of 0 and a maximum score of 50. The weekly average score for the 7 days was calculated for each individual item and the GI summary score was created from these weekly averages. Higher scores indicated worse symptoms. A meaningful difference between two treatment arms was determined to be 0.3 point. (NCT02125877)
Timeframe: weeks -1, 4, 8, 12, 16, 20, 24

,
Interventionscore on a scale (Mean)
week -1 (n=69,65)week 4 (n=60,64)week 8 (n=59,51)week 12 (n=51,45)week 16 (n=48,41)week 20 (n40,39)week 24 (n32,26)
Deferasirox Dispersible Tablet (DFX-DT)1.41.81.41.71.91.51.5
Deferasirox Film-coated Tablet (DFX-FCT)1.91.11.11.00.90.91.2

Weekly Dose Violation Rate

The dose violation is defined as a dose either missed completely or not taken in accordance with the timing instruction (no later than 12:00 pm. The rate was calculated as [number of dose violations/drug exposure (days)] x 100. (NCT02125877)
Timeframe: weeks 1, 4, 8, 12, 16, 20, 24

,
Interventionpercent dose violation (Mean)
week 1 (n=56,53)week 4 (n=58,58)week 8 (n=56,46)week 12 (n=50,41)week 16 (n=48,40)week 20 (n=40,36)week 24 (n=30,24)
Deferasirox Dispersible Tablet (DFX-DT)17.715.818.015.713.522.617.1
Deferasirox Film-coated Tablet (DFX-FCT)15.86.78.410.710.011.310.1

Change in Serum Creatinine During 12 Months Combined Chelation Therapy

Comparison of average serum creatinine over 12 months of combined chelation therapy compared with baseline serum creatinine. (NCT00901199)
Timeframe: 12 months

Interventionmg/dl (Mean)
Deferasirox (Exjade) and Desferal (DFO)0.09

Efficacy of Combined Treatment With Deferasirox and Deferoxamine Over 12 Months

Change in liver iron concentration from baseline to 12 months with the use of combined chelation therapy. The change was calculated as the liver iron concentration at 12 months minus the value at baseline. (NCT00901199)
Timeframe: 12 months

Interventionmg/g (Median)
Deferasirox (Exjade) and Desferal (DFO)-6.2

Reviews

82 reviews available for deferoxamine and Thalassemias

ArticleYear
Benefits and Risks in Polypathology and Polypharmacotherapy Challenges in the Era of the Transition of Thalassaemia from a Fatal to a Chronic or Curable Disease.
    Frontiers in bioscience (Elite edition), 2022, 07-12, Volume: 14, Issue:3

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Humans; Iron; Iron Chelating Agents; Pyridones; R

2022
Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia.
    The Cochrane database of systematic reviews, 2023, 03-06, Volume: 3

    Topics: Anemia, Sickle Cell; Chelating Agents; Chelation Therapy; Child; Deferoxamine; Drug-Related Side Eff

2023
Clinical Challenges with Iron Chelation in Beta Thalassemia.
    Hematology/oncology clinics of North America, 2023, Volume: 37, Issue:2

    Topics: beta-Thalassemia; Deferiprone; Deferoxamine; Humans; Iron; Iron Chelating Agents; Iron Overload; Pyr

2023
Deferasirox for managing iron overload in people with thalassaemia.
    The Cochrane database of systematic reviews, 2017, 08-15, Volume: 8

    Topics: Administration, Oral; Benzoates; Clinical Trials, Phase II as Topic; Clinical Trials, Phase III as T

2017
Efficacy and safety of iron chelators in thalassemia and sickle cell disease: a multiple treatment comparison network meta-analysis and trial sequential analysis.
    Expert review of clinical pharmacology, 2018, Volume: 11, Issue:6

    Topics: Anemia, Sickle Cell; Benzoates; Deferasirox; Deferiprone; Deferoxamine; Drug Therapy, Combination; H

2018
Comparison of Deferiprone to Deferasirox and Deferoxamine to Cardiac and Hepatic T2* MRI in Thalassemia Patients: Evidence-based Case Report.
    Acta medica Indonesiana, 2018, Volume: 50, Issue:2

    Topics: Benzoates; Child; Deferasirox; Deferiprone; Deferoxamine; Drug Therapy, Combination; Heart; Humans;

2018
The Role of Deferiprone in Iron Chelation.
    The New England journal of medicine, 2018, 11-29, Volume: 379, Issue:22

    Topics: Anemia, Sickle Cell; Chelation Therapy; Deferiprone; Deferoxamine; Drug Therapy, Combination; Erythr

2018
Effectiveness and Safety of Deferasirox in Thalassemia with Iron Overload: A Meta-Analysis.
    Acta haematologica, 2019, Volume: 141, Issue:1

    Topics: Databases, Factual; Deferasirox; Deferoxamine; Dose-Response Relationship, Drug; Humans; Iron; Iron

2019
Management of the thalassemias.
    Cold Spring Harbor perspectives in medicine, 2013, Jun-01, Volume: 3, Issue:6

    Topics: Benzoates; Blood Transfusion; Deferasirox; Deferiprone; Deferoxamine; Ferritins; Humans; Iron; Iron

2013
Desferrioxamine mesylate for managing transfusional iron overload in people with transfusion-dependent thalassaemia.
    The Cochrane database of systematic reviews, 2013, Aug-21, Issue:8

    Topics: Benzoates; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents;

2013
Oral deferiprone for iron chelation in people with thalassaemia.
    The Cochrane database of systematic reviews, 2013, Aug-21, Issue:8

    Topics: Administration, Oral; Chelation Therapy; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; I

2013
Comparative efficacy and safety of deferoxamine, deferiprone and deferasirox on severe thalassemia: a meta-analysis of 16 randomized controlled trials.
    PloS one, 2013, Volume: 8, Issue:12

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Ferritins; Humans; Iron; Iron Chelating Agents; L

2013
Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes.
    Drug design, development and therapy, 2016, Volume: 10

    Topics: Benzoates; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents;

2016
Clinical Management of Patients With Thalassemia Syndromes.
    Clinical journal of oncology nursing, 2016, Jun-01, Volume: 20, Issue:3

    Topics: Benzoates; Chelation Therapy; Deferoxamine; Female; Humans; Iron Chelating Agents; Iron Overload; Ma

2016
Mechanisms of and obstacles to iron cardiomyopathy in thalassemia.
    Frontiers in bioscience : a journal and virtual library, 2008, May-01, Volume: 13

    Topics: Blood Pressure; Cardiomyopathies; Deferoxamine; Electrocardiography; Heart; Heart Failure; Humans; I

2008
An update on disordered iron metabolism and iron overload.
    Hematology (Amsterdam, Netherlands), 2010, Volume: 15, Issue:5

    Topics: Animals; Blood Transfusion; Deferiprone; Deferoxamine; Drug Therapy, Combination; Humans; Iron; Iron

2010
Iron overload in thalassemia and related conditions: therapeutic goals and assessment of response to chelation therapies.
    Hematology/oncology clinics of North America, 2010, Volume: 24, Issue:6

    Topics: Benzoates; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine; Ferritins; Humans; Iron; Iron

2010
Deferasirox for managing iron overload in people with thalassaemia.
    The Cochrane database of systematic reviews, 2012, Feb-15, Issue:2

    Topics: Benzoates; Clinical Trials, Phase II as Topic; Clinical Trials, Phase III as Topic; Deferasirox; Def

2012
Iron mobilization using chelation and phlebotomy.
    Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS), 2012, Volume: 26, Issue:2-3

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Humans; Iron; Iron Chelating Agents; Iron Overloa

2012
Hematopoietic stem cell transplantation for thalassemia.
    Immunotherapy, 2012, Volume: 4, Issue:9

    Topics: Blood Transfusion; Deferoxamine; Graft vs Host Disease; Hematopoietic Stem Cell Transplantation; Hum

2012
Results of long term iron chelation treatment with deferoxamine.
    Advances in experimental medicine and biology, 2002, Volume: 509

    Topics: Deferoxamine; Ear, Inner; Endocrine System Diseases; Eye; Heart Diseases; History, 20th Century; Hum

2002
Benefits and risks of deferiprone in iron overload in Thalassaemia and other conditions: comparison of epidemiological and therapeutic aspects with deferoxamine.
    Drug safety, 2003, Volume: 26, Issue:8

    Topics: Deferoxamine; Erythrocyte Transfusion; Humans; Iron Chelating Agents; Iron Overload; Risk; Thalassem

2003
Pharmacotherapy of iron overload in thalassaemic patients.
    Expert opinion on pharmacotherapy, 2003, Volume: 4, Issue:10

    Topics: Clinical Trials as Topic; Deferiprone; Deferoxamine; Drug Therapy, Combination; Ferritins; Humans; I

2003
Combined use of oral chelators and desferrioxamine in thalassemia.
    Hematology (Amsterdam, Netherlands), 2005, Volume: 10 Suppl 1

    Topics: Chelating Agents; Deferoxamine; Drug Therapy, Combination; Humans; Thalassemia; Treatment Outcome

2005
Desferrioxamine mesylate for managing transfusional iron overload in people with transfusion-dependent thalassaemia.
    The Cochrane database of systematic reviews, 2005, Oct-19, Issue:4

    Topics: Chelation Therapy; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; Iron Overload; Pyridone

2005
Advances in iron overload therapies. prospects for effective use of deferiprone (L1), deferoxamine, the new experimental chelators ICL670, GT56-252, L1NA11 and their combinations.
    Current medicinal chemistry, 2005, Volume: 12, Issue:23

    Topics: Benzoates; Carboxylic Acids; Deferasirox; Deferiprone; Deferoxamine; Drug Therapy, Combination; Hemo

2005
Objectives and mechanism of iron chelation therapy.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Animals; Benzoates; Cardiomyopathies; Cells, Cultured; Chelation Therapy; Clinical Trials as Topic;

2005
Recent insights into interactions of deferoxamine with cellular and plasma iron pools: Implications for clinical use.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Animals; Body Fluid Compartments; Chelation Therapy; Chemical Phenomena; Chemistry, Physical; Defero

2005
Combined therapy with deferoxamine and deferiprone.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Agranulocytosis; Biological Transport; Cardiomyopathies; Chelation Therapy; Clinical Trials as Topic

2005
Deferiprone: New insight.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Agranulocytosis; Cardiomyopathies; Clinical Trials as Topic; Deferiprone; Deferoxamine; Follow-Up St

2005
Quality of life in thalassemia.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Adolescent; Adult; Caregivers; Chelating Agents; Chelation Therapy; Child; Child, Preschool; Cyprus;

2005
Monitoring long-term efficacy of iron chelation treatment with biomagnetic liver susceptometry.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Algorithms; Benzoates; Blood Transfusion; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine;

2005
T2* magnetic resonance and myocardial iron in thalassemia.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Adult; Calibration; Cardiomyopathies; Chelation Therapy; Child; Cohort Studies; Combined Modality Th

2005
Future chelation monotherapy and combination therapy strategies in thalassemia and other conditions. comparison of deferiprone, deferoxamine, ICL670, GT56-252, L1NAll and starch deferoxamine polymers.
    Hemoglobin, 2006, Volume: 30, Issue:2

    Topics: Benzoates; Carboxylic Acids; Chelation Therapy; Clinical Trials as Topic; Deferasirox; Deferiprone;

2006
Oral deferiprone for iron chelation in people with thalassaemia.
    The Cochrane database of systematic reviews, 2007, Jul-18, Issue:3

    Topics: Chelation Therapy; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; Iron Overload; Pyridone

2007
Consequences and costs of noncompliance with iron chelation therapy in patients with transfusion-dependent thalassemia: a literature review.
    Transfusion, 2007, Volume: 47, Issue:10

    Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Cost of Illness; Deferiprone; Deferoxamine; Humans

2007
Ethical issues and risk/benefit assessment of iron chelation therapy: advances with deferiprone/deferoxamine combinations and concerns about the safety, efficacy and costs of deferasirox.
    Hemoglobin, 2008, Volume: 32, Issue:1-2

    Topics: Benzoates; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine; Drug Approval; Drug Therapy, C

2008
Effects of chelation therapy on cardiac function improvement in thalassemia patients: literature review and the Taiwanese experience.
    Hemoglobin, 2008, Volume: 32, Issue:1-2

    Topics: Cardiomyopathies; Chelation Therapy; Deferiprone; Deferoxamine; Ferritins; Humans; Iron; Iron Chelat

2008
Treatment of iron overload.
    Seminars in liver disease, 1984, Volume: 4, Issue:3

    Topics: Bloodletting; Carcinoma, Hepatocellular; Deferoxamine; Hemochromatosis; Humans; Liver; Liver Cirrhos

1984
Advances in thalassemia research.
    Blood, 1984, Volume: 63, Issue:4

    Topics: Animals; Base Sequence; Blood Transfusion; Bone Marrow Transplantation; Chemical Phenomena; Chemistr

1984
[Iron chelation. Biological significance and medical application].
    Schweizerische medizinische Wochenschrift, 1983, Oct-08, Volume: 113, Issue:40

    Topics: Animals; Bacterial Infections; Catechols; Deferoxamine; Diabetes Mellitus; Enterobactin; Female; Hum

1983
Clinical removal of iron.
    Annual review of medicine, 1982, Volume: 33

    Topics: Adult; Anemia, Sideroblastic; Bloodletting; Carcinoma, Hepatocellular; Deferoxamine; Diet; Erythropo

1982
Iron overload disorders: natural history, pathogenesis, diagnosis, and therapy.
    Critical reviews in clinical laboratory sciences, 1983, Volume: 19, Issue:3

    Topics: Anemia, Hypochromic; Biological Transport; Bloodletting; Chelating Agents; Deferoxamine; Disease Mod

1983
The role of ascorbic acid in the turnover of storage iron.
    Seminars in hematology, 1983, Volume: 20, Issue:2

    Topics: Adult; Animals; Ascorbic Acid; Deferoxamine; Ferritins; Guinea Pigs; Haplorhini; Hemochromatosis; He

1983
Clinical management of thalassemia. The status of new iron chelators.
    Annals of the New York Academy of Sciences, 1980, Volume: 344

    Topics: Animals; Chelating Agents; Chemical Phenomena; Chemistry; Cholic Acids; Deferoxamine; Drug Evaluatio

1980
[Recommendations for therapy of juvenile thalassemia major].
    Fortschritte der Medizin, 1980, Nov-27, Volume: 98, Issue:44

    Topics: Ascorbic Acid; Blood Transfusion; Child; Deferoxamine; Female; Germany, West; Greece; Hemosiderosis;

1980
Recognition and treatment of iron overload.
    Advances in internal medicine, 1980, Volume: 26

    Topics: Adult; Blood Grouping and Crossmatching; Bloodletting; Costs and Cost Analysis; Deferoxamine; Ethyle

1980
Problems related to treatment of beta-thalassaemia major.
    Paediatrician, 1982, Volume: 11, Issue:3-4

    Topics: Adolescent; Adult; Bone Diseases; Child; Child, Preschool; Deferoxamine; Encephalitis; Female; Hormo

1982
Chelation therapy in beta-thalassemia: the benefits and limitations of desferrioxamine.
    Seminars in hematology, 1995, Volume: 32, Issue:4

    Topics: Adolescent; Adult; Chelating Agents; Chelation Therapy; Child; Deferoxamine; Growth Disorders; Heari

1995
Results of long-term iron-chelating therapy.
    Acta haematologica, 1996, Volume: 95, Issue:1

    Topics: Adolescent; Adult; Deferoxamine; Female; Ferritins; Hemosiderosis; Humans; Iron Chelating Agents; Ma

1996
Iron chelators for thalassaemia.
    British journal of haematology, 1998, Volume: 101, Issue:3

    Topics: Administration, Oral; Aza Compounds; Chelating Agents; Deferiprone; Deferoxamine; Edetic Acid; Human

1998
Pathophysiology of iron overload.
    Annals of the New York Academy of Sciences, 1998, Jun-30, Volume: 850

    Topics: Animals; Cardiomyopathies; Deferoxamine; Free Radicals; Humans; Iron; Siderosis; Thalassemia; Transf

1998
The controversial role of deferiprone in the treatment of thalassemia.
    The Journal of laboratory and clinical medicine, 2001, Volume: 137, Issue:5

    Topics: Agranulocytosis; Arthralgia; Clinical Trials as Topic; Deferiprone; Deferoxamine; Drug Therapy, Comb

2001
Iron overload: clinical and pathologic aspects in pediatrics.
    Seminars in hematology, 1977, Volume: 14, Issue:1

    Topics: Abnormalities, Multiple; Adolescent; Adult; Ascorbic Acid Deficiency; Bloodletting; Child; Child, Pr

1977
Chelation therapy for the treatment of thalassemia.
    Seminars in hematology, 1977, Volume: 14, Issue:1

    Topics: Chelating Agents; Deferoxamine; Humans; Hydroxamic Acids; Hydroxybenzoates; Pentetic Acid; Rhodotoru

1977
Current problems of iron overload.
    Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer, 1979, Volume: 69

    Topics: Deferoxamine; Diet; Hemochromatosis; Humans; Iron; Thalassemia; Tissue Distribution

1979
Thalassemia major: molecular and clinical aspects. NIH Conference.
    Annals of internal medicine, 1979, Volume: 91, Issue:6

    Topics: Blood Transfusion; Chelating Agents; Deferoxamine; DNA; Genes; Globins; Heart; Hemoglobins; Humans;

1979
Advances in the use of iron-chelating agents for the treatment of iron overload.
    Progress in hematology, 1979, Volume: 11

    Topics: Adolescent; Adult; Anemia; Child; Child, Preschool; Deferoxamine; Female; Ferritins; Heart; Hemochro

1979
Management of thalassaemia major.
    British medical bulletin, 1976, Volume: 32, Issue:3

    Topics: Blood Transfusion; Child; Deferoxamine; Ethnicity; Female; Ferritins; Hemoglobins; Humans; Iron; Mal

1976
Thalassemia in Britain and Australia.
    Birth defects original article series, 1976, Volume: 12, Issue:8

    Topics: Adolescent; Australia; Chelating Agents; Deferoxamine; Humans; Iron; Liver; Puberty; Thalassemia; Tr

1976
Evaluation of desferrioxamine and ascorbic acid for the treatment of chronic iron overload.
    Birth defects original article series, 1976, Volume: 12, Issue:8

    Topics: Adolescent; Adult; Aged; Anemia; Ascorbic Acid; Deferoxamine; Drug Evaluation; Feces; Humans; Iron;

1976
Thalassemia.
    Annual review of medicine, 1975, Volume: 26

    Topics: Blood Transfusion; Bone Marrow Examination; Deferoxamine; Diagnosis, Differential; Erythrocyte Count

1975
Management of thalassemia major (Cooley's anemia).
    Hematology/oncology clinics of North America, 1991, Volume: 5, Issue:3

    Topics: Blood Transfusion; Bone Marrow Transplantation; Chelation Therapy; Deferoxamine; Humans; Iron; Thala

1991
The management of haemoglobinopathies.
    Bailliere's clinical haematology, 1991, Volume: 4, Issue:2

    Topics: Adolescent; Anemia, Sickle Cell; Bone Marrow Transplantation; Chelation Therapy; Child; Child, Presc

1991
Iron and lymphocytes: reciprocal regulatory interactions.
    Current studies in hematology and blood transfusion, 1991, Issue:58

    Topics: Animals; Bloodletting; CD4-CD8 Ratio; Chelation Therapy; Deferoxamine; Ferric Compounds; Hemochromat

1991
Iron chelation.
    Blood reviews, 1990, Volume: 4, Issue:1

    Topics: Administration, Oral; Chelation Therapy; Deferoxamine; Drug Design; Drug Evaluation; Free Radicals;

1990
Oral iron chelators.
    Seminars in hematology, 1990, Volume: 27, Issue:2

    Topics: Administration, Oral; Chelation Therapy; Deferoxamine; Humans; Iron Chelating Agents; Thalassemia; T

1990
Current status of iron chelation therapy with deferoxamine.
    Seminars in hematology, 1990, Volume: 27, Issue:2

    Topics: Chelation Therapy; Deferoxamine; Humans; Iron Chelating Agents; Thalassemia; Transfusion Reaction

1990
Desferrioxamine: its use in iron chelation in thalassemia.
    Indian pediatrics, 1990, Volume: 27, Issue:3

    Topics: Chelation Therapy; Child, Preschool; Deferoxamine; Humans; Iron; Thalassemia

1990
Current therapy of Cooley's anemia. A decade of experience with subcutaneous desferrioxamine.
    Annals of the New York Academy of Sciences, 1990, Volume: 612

    Topics: Blood Transfusion; Deferoxamine; Humans; Infusions, Parenteral; Splenectomy; Thalassemia

1990
[Iron-chelating treatment].
    Haematologica, 1989, Volume: 74, Issue:5 Suppl

    Topics: Chelation Therapy; Deferiprone; Deferoxamine; Erythropoiesis; Hemosiderosis; Humans; Iron; Iron Chel

1989
Beta-thalassaemia--the Johannesburg experience.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1989, Apr-15, Volume: 75, Issue:8

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Erythrocyte Transfusion

1989
Results of long-term subcutaneous desferrioxamine therapy.
    Bailliere's clinical haematology, 1989, Volume: 2, Issue:2

    Topics: Deferoxamine; Hemosiderosis; Humans; Infusion Pumps; Infusions, Intravenous; Thalassemia

1989
Biological and toxic properties of deferoxamine.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Cataract; Cell Division; Deferoxamine; DNA; Drug Hypersensitivity; Hearing Disorders; Humans; Pulmon

1989
Iron chelation.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Animals; Blood Transfusion; Cells, Cultured; Deferoxamine; Free Radicals; Heart; Humans; In Vitro Te

1989
Measurement of iron status.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Blood Transfusion; Deferoxamine; Ferritins; Humans; Intestinal Absorption; Iron; Iron Chelating Agen

1989
Management of beta-thalassemia major using transfusions and iron chelation with deferoxamine.
    Transfusion medicine reviews, 1988, Volume: 2, Issue:3

    Topics: Blood Component Transfusion; Blood Transfusion; Deferoxamine; Humans; Iron; Thalassemia

1988
Iron overload and iron chelation therapy in thalassaemia and sickle cell haemoglobinopathies.
    Acta haematologica, 1987, Volume: 78, Issue:2-3

    Topics: Anemia, Sickle Cell; Ascorbic Acid; Deferoxamine; Drug Administration Schedule; Forecasting; Humans;

1987
Modern management of thalassemia.
    Pediatric annals, 1985, Volume: 14, Issue:9

    Topics: Adolescent; Arrhythmias, Cardiac; Ascorbic Acid; Blood Transfusion; Child; Cholelithiasis; Deferoxam

1985
Transfusional iron overload.
    Clinical and laboratory haematology, 1985, Volume: 7, Issue:3

    Topics: Ascorbic Acid; Blood Transfusion; Deferoxamine; Endocrine Glands; Heart; Humans; Infusions, Parenter

1985
[Use of desferal in treatment of sideroses of different origin. (Literature review)].
    Problemy gematologii i perelivaniia krovi, 1968, Volume: 13, Issue:7

    Topics: Anemia; Anemia, Aplastic; Anemia, Sideroblastic; Animals; Bile; Child, Preschool; Deferoxamine; Hemo

1968
Clinical usefulness of iron chelating agents.
    Progress in hematology, 1969, Volume: 6

    Topics: Chelating Agents; Deferoxamine; Dimercaprol; Edetic Acid; Hemochromatosis; Humans; Iron; Iron Chelat

1969

Trials

29 trials available for deferoxamine and Thalassemias

ArticleYear
Deferiprone vs deferoxamine for transfusional iron overload in SCD and other anemias: a randomized, open-label noninferiority study.
    Blood advances, 2022, 02-22, Volume: 6, Issue:4

    Topics: Adolescent; Anemia, Sickle Cell; Blood Transfusion; Deferiprone; Deferoxamine; Female; Humans; Iron

2022
Patient-reported outcomes from a randomized phase II study of the deferasirox film-coated tablet in patients with transfusion-dependent anemias.
    Health and quality of life outcomes, 2018, Nov-19, Volume: 16, Issue:1

    Topics: Adult; Blood Transfusion; Chelation Therapy; Deferoxamine; Female; Humans; Iron Chelating Agents; Ir

2018
Long-term sequential deferiprone-deferoxamine versus deferiprone alone for thalassaemia major patients: a randomized clinical trial.
    British journal of haematology, 2009, Volume: 145, Issue:2

    Topics: Administration, Oral; Adolescent; Adult; Deferiprone; Deferoxamine; Drug Therapy, Combination; Femal

2009
Reduction of body iron stores to normal range levels in thalassaemia by using a deferiprone/deferoxamine combination and their maintenance thereafter by deferiprone monotherapy.
    European journal of haematology, 2010, Volume: 85, Issue:5

    Topics: Adult; Deferiprone; Deferoxamine; Drug Therapy, Combination; Female; Ferritins; Humans; Iron; Iron C

2010
Combined chelation therapy with deferasirox and deferoxamine in thalassemia.
    Blood cells, molecules & diseases, 2013, Volume: 50, Issue:2

    Topics: Adolescent; Adult; Benzoates; Chelation Therapy; Child; Deferasirox; Deferoxamine; Drug Synergism; F

2013
Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs.
    Journal of bone and mineral metabolism, 2004, Volume: 22, Issue:1

    Topics: Adolescent; Alkaline Phosphatase; Amino Acids; Body Weights and Measures; Bone and Bones; Bone Densi

2004
Comparative efficacy of desferrioxamine, deferiprone and in combination on iron chelation in thalassemic children.
    Indian pediatrics, 2004, Volume: 41, Issue:1

    Topics: Blood Transfusion; Child; Deferiprone; Deferoxamine; Drug Therapy, Combination; Ferritins; Humans; I

2004
New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years.
    Blood, 2004, Aug-15, Volume: 104, Issue:4

    Topics: Adolescent; Age Factors; Antineoplastic Agents; Bone Marrow Transplantation; Chelating Agents; Child

2004
Comparison of subcutaneous infusion needles for transfusion-dependent thalassemia patients by the intrapersonal cross-over assessment model.
    American journal of hematology, 2004, Volume: 76, Issue:4

    Topics: Adolescent; Adult; Chelation Therapy; Child; Cross-Over Studies; Deferoxamine; Edema; Equipment Desi

2004
A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemia.
    Haematologica, 2006, Volume: 91, Issue:9

    Topics: Adolescent; Adult; Deferiprone; Deferoxamine; Drug Therapy, Combination; Female; Humans; Iron Overlo

2006
Iron chelation in thalassemia: combined or monotherapy? The Egyptian experience.
    Annals of hematology, 2008, Volume: 87, Issue:7

    Topics: Adolescent; Adult; Chelation Therapy; Child; Child, Preschool; Deferiprone; Deferoxamine; Drug Admin

2008
Oral desferrioxamine in young patients with thalassaemia.
    Lancet (London, England), 1981, Jan-03, Volume: 1, Issue:8210

    Topics: Administration, Oral; Child, Preschool; Deferoxamine; Hemosiderosis; Humans; Thalassemia; Transfusio

1981
Survival and desferrioxamine in thalassaemia major.
    British medical journal (Clinical research ed.), 1982, Apr-10, Volume: 284, Issue:6322

    Topics: Adolescent; Adult; Child; Child, Preschool; Clinical Trials as Topic; Deferoxamine; Dose-Response Re

1982
Growth velocity monitoring of the efficacy of different therapeutic protocols in a group of thalassaemic children.
    European journal of pediatrics, 1995, Volume: 154, Issue:3

    Topics: Chelation Therapy; Child; Child, Preschool; Chronic Disease; Deferoxamine; Female; Ferritins; Follow

1995
Phlebotomy to reduce iron overload in patients cured of thalassemia by bone marrow transplantation. Italian Cooperative Group for Phlebotomy Treatment of Transplanted Thalassemia Patients.
    Blood, 1997, Aug-01, Volume: 90, Issue:3

    Topics: Adolescent; Bone Marrow Transplantation; Chelation Therapy; Child; Combined Modality Therapy; Defero

1997
Combined therapy with deferiprone and desferrioxamine.
    British journal of haematology, 1998, Volume: 103, Issue:2

    Topics: Adolescent; Adult; Aged; beta-Thalassemia; Deferiprone; Deferoxamine; Dose-Response Relationship, Dr

1998
Efficacy and side effects of deferiprone (L1) in thalassemia patients not compliant with desferrioxamine.
    Acta haematologica, 1999, Volume: 101, Issue:4

    Topics: Adolescent; Adult; Arthralgia; Child; Deferiprone; Deferoxamine; Female; Ferritins; Follow-Up Studie

1999
Subcutaneous infusion and intramuscular injection of desferrioxamine in patients with transfusional iron overload.
    Lancet (London, England), 1976, Dec-11, Volume: 2, Issue:7998

    Topics: Adolescent; Adult; Anemia, Sideroblastic; Blood Transfusion; Child; Circadian Rhythm; Deferoxamine;

1976
Chelation therapy in beta-thalassemia major. I. Intravenous and subcutaneous deferoxamine.
    The Journal of pediatrics, 1978, Volume: 92, Issue:4

    Topics: Adolescent; Adult; Age Factors; Antipyrine; Child; Child, Preschool; Deferoxamine; Dose-Response Rel

1978
Editorial: "Propper" use of desferrioxamine.
    The New England journal of medicine, 1976, Jun-24, Volume: 294, Issue:26

    Topics: Clinical Trials as Topic; Deferoxamine; Humans; Infusions, Parenteral; Thalassemia

1976
Effect of pentoxifylline on treatment of lower limb ulcers in patients with thalassemia major.
    Angiology, 1992, Volume: 43, Issue:7

    Topics: Adult; Deferoxamine; Female; Humans; Leg Ulcer; Male; Pentoxifylline; Recurrence; Thalassemia

1992
Efficacy and possible adverse effects of the oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one (L1) in thalassemia major.
    Blood, 1992, Aug-01, Volume: 80, Issue:3

    Topics: Adult; Deferiprone; Deferoxamine; Female; Ferritins; Follow-Up Studies; Humans; Iron; Iron Chelating

1992
Pituitary function in thalassemic patients and the effect of chelation therapy.
    Acta endocrinologica, 1991, Volume: 124, Issue:1

    Topics: Adult; Chelation Therapy; Deferoxamine; Female; Ferritins; Follicle Stimulating Hormone; Follow-Up S

1991
Comparison of oral iron chelator L1 and desferrioxamine in iron-loaded patients.
    Lancet (London, England), 1990, Nov-24, Volume: 336, Issue:8726

    Topics: Adolescent; Adult; Anemia, Aplastic; Animals; Blood Transfusion; Child; Cohort Studies; Combined Mod

1990
Studies of the oral chelator 1,2-dimethyl-3-hydroxypyrid-4-one in thalassemia patients.
    Seminars in hematology, 1990, Volume: 27, Issue:2

    Topics: Administration, Oral; Adolescent; Adult; Chelation Therapy; Child; Deferiprone; Deferoxamine; Drug A

1990
Evaluation of the oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one (L1) in iron-loaded patients.
    Annals of the New York Academy of Sciences, 1990, Volume: 612

    Topics: Administration, Oral; Adult; Deferiprone; Deferoxamine; Humans; Iron; Iron Chelating Agents; Pyridon

1990
Noncompliance with iron chelation therapy in patients with beta thalassaemia.
    Journal of psychosomatic research, 1989, Volume: 33, Issue:6

    Topics: Administration, Cutaneous; Adolescent; Adult; Blood Transfusion; Child; Clinical Trials as Topic; De

1989
Effective chelation of iron in beta thalassaemia with the oral chelator 1,2-dimethyl-3-hydroxypyrid-4-one.
    British medical journal (Clinical research ed.), 1987, Dec-12, Volume: 295, Issue:6612

    Topics: Administration, Oral; Adolescent; Adult; Aged; Ascorbic Acid; Clinical Trials as Topic; Deferiprone;

1987
Long-term chelation therapy in thalassaemia major: effect on liver iron concentration, liver histology, and clinical progress.
    British medical journal, 1974, Apr-06, Volume: 2, Issue:5909

    Topics: Biopsy; Blood Transfusion; Chelating Agents; Child; Deferoxamine; Diethylamines; Female; Humans; Iro

1974

Other Studies

377 other studies available for deferoxamine and Thalassemias

ArticleYear
Lifting the iron curtain of vision.
    EMBO molecular medicine, 2023, 02-08, Volume: 15, Issue:2

    Topics: Deferoxamine; Humans; Iron Chelating Agents; Lifting; Thalassemia

2023
An evaluation of deferiprone as twice-a-day tablets or in combination therapy for the treatment of transfusional iron overload in thalassemia syndromes.
    Expert review of hematology, 2023, Volume: 16, Issue:2

    Topics: Benzoates; Blood Transfusion; Deferasirox; Deferoxamine; Humans; Iron Chelating Agents; Iron Overloa

2023
Combined chelation with high-dose deferiprone and deferoxamine to improve survival and restore cardiac function effectively in patients with transfusion-dependent thalassemia presenting severe cardiac complications.
    Annals of hematology, 2020, Volume: 99, Issue:10

    Topics: Arrhythmias, Cardiac; Blood Transfusion; Chelation Therapy; Deferiprone; Deferoxamine; Drug Evaluati

2020
Using of deferasirox and deferoxamine in refractory iron overload thalassemia.
    Pediatrics international : official journal of the Japan Pediatric Society, 2021, Volume: 63, Issue:4

    Topics: Benzoates; beta-Thalassemia; Deferasirox; Deferoxamine; Humans; Iron Chelating Agents; Iron Overload

2021
Economic burden in the management of transfusion-dependent thalassaemia patients in Malaysia from a societal perspective.
    Orphanet journal of rare diseases, 2021, 04-07, Volume: 16, Issue:1

    Topics: Benzoates; Blood Transfusion; Cost of Illness; Cross-Sectional Studies; Deferasirox; Deferoxamine; H

2021
Serum Zinc Level in β-Thalassemia Major: A Retrospective Study in Southwest Iran.
    Hemoglobin, 2021, Volume: 45, Issue:2

    Topics: Adult; Benzoates; beta-Thalassemia; Cross-Sectional Studies; Deferasirox; Deferiprone; Deferoxamine;

2021
Thalassemia: Yesterday, Today, Tomorrow.
    American journal of hematology, 2017, Volume: 92, Issue:6

    Topics: Attitude of Health Personnel; Attitude to Health; Chelation Therapy; Cyprus; Deferiprone; Deferoxami

2017
The aim of iron chelation therapy in thalassaemia.
    European journal of haematology, 2017, Volume: 99, Issue:5

    Topics: beta-Thalassemia; Chelation Therapy; Deferoxamine; Humans; Iron; Iron Chelating Agents; Iron Overloa

2017
Chelation protocols for the elimination and prevention of iron overload in thalassaemia.
    Frontiers in bioscience (Landmark edition), 2018, 01-01, Volume: 23, Issue:6

    Topics: Benzoates; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine; Drug Therapy, Combination; Hum

2018
The effect of desferrioxamine chelation versus no therapy in patients with non transfusion-dependent thalassaemia: a multicenter prospective comparison from the MIOT network.
    Annals of hematology, 2018, Volume: 97, Issue:10

    Topics: Adolescent; Adult; Aged; Chelation Therapy; Child; Deferoxamine; Female; Follow-Up Studies; Heart; H

2018
Pattern dystrophies in patients treated with deferoxamine: report of two cases and review of the literature.
    BMC ophthalmology, 2018, Sep-12, Volume: 18, Issue:1

    Topics: Deferoxamine; Electroretinography; Female; Humans; Infusions, Subcutaneous; Middle Aged; Retina; Ret

2018
A pharmaco-economic evaluation of deferasirox for treating patients with iron overload caused by transfusion-dependent thalassemia in Taiwan.
    Journal of the Formosan Medical Association = Taiwan yi zhi, 2013, Volume: 112, Issue:4

    Topics: Benzoates; Child, Preschool; Deferasirox; Deferoxamine; Health Care Costs; Humans; Iron Chelating Ag

2013
A record number of fatalities in many categories of patients treated with deferasirox: loopholes in regulatory and marketing procedures undermine patient safety and misguide public funds?
    Expert opinion on drug safety, 2013, Volume: 12, Issue:5

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; Iron Overload; Mar

2013
Impact of psychosocial status and disease knowledge on deferoxamine adherence among thalassaemia major adolescents.
    International journal of nursing practice, 2014, Volume: 20, Issue:3

    Topics: Adolescent; Cross-Sectional Studies; Deferoxamine; Female; Humans; Male; Patient Compliance; Thalass

2014
Deferoxamine retinopathy: spectral domain-optical coherence tomography findings.
    BMC ophthalmology, 2014, Jul-02, Volume: 14

    Topics: Adult; Deferoxamine; Dose-Response Relationship, Drug; Fluorescein Angiography; Fundus Oculi; Humans

2014
Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agents.
    Hemoglobin, 2014, Volume: 38, Issue:5

    Topics: Adolescent; Adult; Benzoates; Chelation Therapy; Child; Child, Preschool; Deferasirox; Deferiprone;

2014
The effects of economic sanctions on disease specific clinical outcomes of patients with thalassemia and hemophilia in Iran.
    Health policy (Amsterdam, Netherlands), 2015, Volume: 119, Issue:2

    Topics: Adolescent; Adult; Benzoates; Child; Child, Preschool; Deferasirox; Deferoxamine; Female; Ferritins;

2015
Cultural preferences and limited public resources influence the spectrum of thalassemia in Egypt.
    Journal of pediatric hematology/oncology, 2015, Volume: 37, Issue:4

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Consanguinity; Culture; Deferoxamine;

2015
Severe bacterial infections in patients with non-transfusion-dependent thalassemia: prevalence and clinical risk factors.
    International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2015, Volume: 39

    Topics: Adolescent; Adult; Bacterial Infections; Child; Deferoxamine; Female; Ferritins; Humans; Iron Overlo

2015
Dual T-type and L-type calcium channel blocker exerts beneficial effects in attenuating cardiovascular dysfunction in iron-overloaded thalassaemic mice.
    Experimental physiology, 2016, Volume: 101, Issue:4

    Topics: Animals; Benzoates; Calcium Channel Blockers; Calcium Channels, L-Type; Calcium Channels, T-Type; Ca

2016
The Italian multiregional thalassemia registry: Centers characteristics, services, and patients' population.
    Hematology (Amsterdam, Netherlands), 2016, Volume: 21, Issue:7

    Topics: Adult; Ambulatory Care Facilities; Blood Transfusion; Chelation Therapy; Deferiprone; Deferoxamine;

2016
Effects of iron overload condition on liver toxicity and hepcidin/ferroportin expression in thalassemic mice.
    Life sciences, 2016, Apr-01, Volume: 150

    Topics: Animals; bcl-2-Associated X Protein; Calcium Channel Blockers; Calcium Channels, L-Type; Calcium Cha

2016
Combination of Oral Iron Chelators for Thalassemia.
    Indian pediatrics, 2016, Volume: 53, Issue:3

    Topics: beta-Thalassemia; Deferoxamine; Humans; Iron; Iron Chelating Agents; Iron Overload; Thalassemia

2016
ELECTRORETINOGRAPHIC AND VISUAL-EVOKED POTENTIAL CHANGES IN RELATION TO CHELATION MODALITY IN CHILDREN WITH THALASSEMIA.
    Retina (Philadelphia, Pa.), 2017, Volume: 37, Issue:6

    Topics: Administration, Oral; Adolescent; Benzoates; Cross-Sectional Studies; Deferasirox; Deferoxamine; Dos

2017
Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes.
    Drug design, development and therapy, 2016, Volume: 10

    Topics: Benzoates; Chelation Therapy; Deferoxamine; Drug Therapy, Combination; Humans; Iron; Iron Chelating

2016
K. pneumoniae liver abscess following deferoxamine subcutaneous self-injection.
    American journal of hematology, 2017, Volume: 92, Issue:5

    Topics: Administration, Oral; Amoxicillin-Potassium Clavulanate Combination; Deferoxamine; Female; Glucoseph

2017
Hepatitis B virus reactivation during combined therapy with deferiprone and desferioxamine in a hepatitis B surface antigen thalassemic carrier.
    International journal of hematology, 2009, Volume: 89, Issue:2

    Topics: Adult; Blood Transfusion; Deferiprone; Deferoxamine; Hepatitis B; Hepatitis B virus; Humans; Iron Ch

2009
Quality of life in transfusion-dependent thalassaemia patients on desferrioxamine treatment.
    Singapore medical journal, 2009, Volume: 50, Issue:8

    Topics: Adolescent; Adult; Blood Transfusion; Child; Cross-Sectional Studies; Deferoxamine; Female; Follow-U

2009
Advances in the prevention and treatment are changing thalassemia from a fatal to a chronic disease. experience from a Cyprus model and its use as a paradigm for future applications.
    Hemoglobin, 2009, Volume: 33, Issue:5

    Topics: Chelation Therapy; Chronic Disease; Cyprus; Deferiprone; Deferoxamine; Female; Ferritins; Genetic Te

2009
Uses and limitations of serum ferritin, magnetic resonance imaging T2 and T2* in the diagnosis of iron overload and in the ferrikinetics of normalization of the iron stores in thalassemia using the International Committee on Chelation deferiprone/deferoxa
    Hemoglobin, 2009, Volume: 33, Issue:5

    Topics: Adolescent; Adult; Chelation Therapy; Child; Deferiprone; Deferoxamine; Diagnosis, Differential; Dru

2009
A new era in iron chelation therapy: the design of optimal, individually adjusted iron chelation therapies for the complete removal of iron overload in thalassemia and other chronically transfused patients.
    Hemoglobin, 2009, Volume: 33, Issue:5

    Topics: Blood Transfusion; Chelation Therapy; Clinical Protocols; Deferiprone; Deferoxamine; Drug Therapy, C

2009
Effects of chelators (deferoxamine, deferiprone and deferasirox) on the growth of Klebsiella pneumoniae and Aeromonas hydrophila isolated from transfusion-dependent thalassemia patients.
    Hemoglobin, 2009, Volume: 33, Issue:5

    Topics: Aeromonas hydrophila; Benzoates; Blood Transfusion; Deferasirox; Deferiprone; Deferoxamine; Gram-Neg

2009
Risk/benefit assessment, advantages over other drugs and targeting methods in the use of deferiprone as a pharmaceutical antioxidant in iron loading and non iron loading conditions.
    Hemoglobin, 2009, Volume: 33, Issue:5

    Topics: Animals; Antioxidants; Benzoates; Chelation Therapy; Copper; Deferasirox; Deferiprone; Deferoxamine;

2009
Combining two orally active iron chelators for thalassemia.
    Annals of hematology, 2010, Volume: 89, Issue:11

    Topics: Administration, Oral; Adolescent; Adult; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; P

2010
Retrospective study on the combination of desferrioxamine and deferasirox for treatment of iron-overloaded thalassemic patients: first evidence of more than 2 years.
    Journal of pediatric hematology/oncology, 2010, Volume: 32, Issue:5

    Topics: Adolescent; Adult; Benzoates; Child; Deferasirox; Deferoxamine; Drug Therapy, Combination; Female; F

2010
Incidence of hepatocellular carcinoma in a thalassemia unit.
    Hemoglobin, 2010, Volume: 34, Issue:3

    Topics: Adult; Aged; Antibodies; Carcinoma, Hepatocellular; Chelation Therapy; Deferoxamine; Female; Hepatit

2010
Mechanisms for the shuttling of plasma non-transferrin-bound iron (NTBI) onto deferoxamine by deferiprone.
    Translational research : the journal of laboratory and clinical medicine, 2010, Volume: 156, Issue:2

    Topics: Adult; Chromatography, High Pressure Liquid; Deferiprone; Deferoxamine; Female; Ferric Compounds; Hu

2010
Pathogenesis and management of iron toxicity in thalassemia.
    Annals of the New York Academy of Sciences, 2010, Volume: 1202

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Homeostasis; Humans; Iron; Iron Chelating Agents;

2010
Deferiprone.
    Annals of the New York Academy of Sciences, 2010, Volume: 1202

    Topics: Deferiprone; Deferoxamine; Humans; Iron; Iron Chelating Agents; Liver; Pyridones; Randomized Control

2010
Treatment options for thalassemia patients with osteoporosis.
    Annals of the New York Academy of Sciences, 2010, Volume: 1202

    Topics: Antineoplastic Agents; Bone Density Conservation Agents; Calcitonin; Clinical Trials as Topic; Defer

2010
Iron chelation in thalassemia: time to reconsider our comfort zones.
    Expert review of hematology, 2011, Volume: 4, Issue:1

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Drug Therapy, Combination; Ferritins; Humans; Iro

2011
Self-reported level of and factors influencing the compliance to desferrioxamine therapy in multitransfused thalassaemias.
    Journal of paediatrics and child health, 2011, Volume: 47, Issue:8

    Topics: Adolescent; Adolescent Behavior; Blood Transfusion; Caregivers; Child; Child Behavior; Child, Presch

2011
Iron chelation adherence to deferoxamine and deferasirox in thalassemia.
    American journal of hematology, 2011, Volume: 86, Issue:5

    Topics: Adolescent; Adult; Age Factors; Benzoates; Chelation Therapy; Child; Child, Preschool; Deferasirox;

2011
Evaluation of myocardial and hepatic iron loading by MRI T2* in multi-transfused patients with repeated blood loss as compared to thalassaemia major patients and controls.
    Blood transfusion = Trasfusione del sangue, 2011, Volume: 9, Issue:3

    Topics: Blood Transfusion; Child, Preschool; Deferoxamine; Female; Gastrointestinal Hemorrhage; Humans; Infa

2011
Health-related quality of life in Thai thalassemic children treated with iron chelation.
    The Southeast Asian journal of tropical medicine and public health, 2011, Volume: 42, Issue:4

    Topics: Adolescent; Age Factors; Benzoates; Child; Child, Preschool; Cross-Sectional Studies; Deferasirox; D

2011
Thalassemia: cardiac iron and chelators.
    Indian pediatrics, 2012, Volume: 49, Issue:4

    Topics: Benzoates; Deferasirox; Deferoxamine; Heart Diseases; Humans; Iron Chelating Agents; Iron Overload;

2012
The proceedings of the 20th International Conference on Chelation held in the USA: advances on new and old chelation therapies.
    Toxicology mechanisms and methods, 2013, Volume: 23, Issue:1

    Topics: Chelating Agents; Chelation Therapy; Deferiprone; Deferoxamine; Edetic Acid; Humans; Iron Overload;

2013
Beliefs about chelation among thalassemia patients.
    Health and quality of life outcomes, 2012, Dec-07, Volume: 10

    Topics: Adolescent; Adult; Chelation Therapy; Child; Child, Preschool; Deferoxamine; Female; Ferritins; Heal

2012
Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation.
    European journal of haematology, 2003, Volume: 70, Issue:6

    Topics: Adolescent; Adult; Arrhythmias, Cardiac; Catheterization, Central Venous; Chelation Therapy; Deferox

2003
Bull's eye maculopathy with deferoxamine.
    European journal of haematology, 2003, Volume: 70, Issue:6

    Topics: Adult; Deferoxamine; Female; Humans; Iron Chelating Agents; Macular Degeneration; Thalassemia

2003
Do we need more iron-chelating drugs?
    Lancet (London, England), 2003, Aug-09, Volume: 362, Issue:9382

    Topics: Benzoates; Deferasirox; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; Iron Overload; Pyr

2003
[PREVENTION OF HYPERACTIVE ERYTHROPOIESIS AS A THERAPEUTIC CRITERION IN THALASSEMIA AND OTHER CORPUSCULAR ANEMIAS. PRELIMINARY NOTE].
    Prensa medica argentina, 1963, Feb-15, Volume: 50

    Topics: Anemia; Blood Transfusion; Deferoxamine; Erythropoiesis; Humans; Hydroxamic Acids; Infant; Splenomeg

1963
THE TREATMENT OF HAEMOCHROMATOSIS WITH DESFERRIOXAMINE.
    Acta haematologica, 1963, Volume: 30

    Topics: Anemia; Anemia, Macrocytic; Deferoxamine; Diabetes Mellitus; Ferritins; Hemochromatosis; Hemoglobins

1963
DESFERRIOXAMINE IN HB-E-THALASSAEMIA DISEASE.
    Bulletin of the Calcutta School of Tropical Medicine, 1963, Volume: 11

    Topics: Chelating Agents; Deferoxamine; Hemoglobinopathies; Hemoglobins; Hemoglobins, Abnormal; Humans; Hydr

1963
[THE USE OF DESFERRIOXAMINE IN THE TREATMENT OF HEMOCHROMATOSIS].
    Jornal do medico, 1964, Apr-25, Volume: 53

    Topics: Anemia; Anemia, Aplastic; Blood Chemical Analysis; Body Fluids; Deferoxamine; Hemochromatosis; Hydro

1964
[ERYTHROBLASTOPHTHISIS].
    Medizinische Klinik, 1964, Mar-20, Volume: 59

    Topics: Adrenal Cortex Hormones; Androgens; Blood Cell Count; Blood Transfusion; Deferoxamine; Electrocardio

1964
SUBSTITUTIVE-INHIBITORY THERAPY IN CONSTITUTIONAL NON-SPHEROCYTIC ERYTHROCYTIC DISEASE.
    Acta haematologica, 1964, Volume: 31

    Topics: Anemia; Anemia, Hemolytic; Anemia, Hemolytic, Congenital Nonspherocytic; Blood Transfusion; Deferoxa

1964
[A NEW TEST FOR ASCERTAINMENT OF STATES OF SIDEROSIS: THE DESFERRIOXAMINE TEST. PRELIMINARY RESULTS].
    Il Policlinico. Sezione pratica, 1964, Jul-20, Volume: 71

    Topics: Anemia; Anemia, Hypochromic; Biomedical Research; Deferoxamine; Hematologic Diseases; Hemochromatosi

1964
[PRELIMINARY NOTE ON THE THERAPEUTIC USE OF DESFERRIOXAMINE IN COOLEY'S DISEASE].
    Minerva pediatrica, 1964, Jun-30, Volume: 16

    Topics: Blood Transfusion; Child; Deferoxamine; Hemochromatosis; Humans; Hydroxamic Acids; Infant; Iron; Tha

1964
ENZYMATIC DEFECTS OF HEME SYNTHESIS IN THALASSEMIA.
    Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119

    Topics: Amino Acid Oxidoreductases; Bone Marrow Examination; Deferoxamine; Drug Therapy; Erythropoiesis; Hem

1964
METABOLISM OF IRON, CALCIUM AND MAGNESIUM IN HOMOZYGOUS THALASSEMIA.
    Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119

    Topics: Adolescent; beta-Thalassemia; Blood; Blood Transfusion; Calcium; Child; Deferoxamine; Drug Therapy;

1964
CHELATING AGENTS IN THE DIAGNOSIS AND TREATMENT OF IRON OVERLOAD IN THALASSEMIA.
    Annals of the New York Academy of Sciences, 1964, Oct-07, Volume: 119

    Topics: Adolescent; Blood Transfusion; Chelating Agents; Child; Deferoxamine; Diagnosis; Drug Therapy; Human

1964
TREATMENT OF PRIMARY AND SECONDARY HEMOCHROMATOSIS AND ACUTE IRON POISONING WITH A NEW POTENT IRON ELIMINATING AGENT (DESFERRIOXAMINE B-DFOM).
    Nederlands tijdschrift voor geneeskunde, 1964, Aug-22, Volume: 108

    Topics: Anemia; Anemia, Aplastic; Anemia, Hemolytic; Anemia, Macrocytic; Deferoxamine; Guinea Pigs; Heavy Me

1964
[TREATMENT OF HEMOSIDEROSIS SECONDARY TO MULTIPLE TRANSFUSIONS, WITH SPECIAL REFERENCE TO COOLEY'S HEMOLYTIC ANEMIA].
    Hospital (Rio de Janeiro, Brazil), 1964, Volume: 66

    Topics: Anemia, Hemolytic; Blood Transfusion; Deferoxamine; Drug Therapy; Hemosiderosis; Humans; Thalassemia

1964
[TREATMENT OF HEMOCHROMATOSIS].
    Deutsche medizinische Wochenschrift (1946), 1965, Feb-19, Volume: 90

    Topics: Deferoxamine; Drug Therapy; Hemochromatosis; Hemosiderosis; Humans; Porphyrias; Thalassemia

1965
[TREATMENT OF SECONDARY HEMOCHROMATOSIS WITH DESFERRIOXAMINE B].
    Acta paediatrica Belgica, 1964, Volume: 18

    Topics: Child; Deferoxamine; Drug Therapy; Hemochromatosis; Humans; Infant; Thalassemia

1964
[TREATMENT OF HEMOCHROMATOSIS CAUSED BY COOLEY'S ANEMIA BY DESFERRIOXAMINE. PRELIMINARY RESULTS].
    La Medecine infantile, 1965, Volume: 72

    Topics: beta-Thalassemia; Deferoxamine; Hemochromatosis; Humans; Thalassemia

1965
Independent clinical trials.
    Lancet (London, England), 2004, Mar-27, Volume: 363, Issue:9414

    Topics: Anemia, Sickle Cell; Deferiprone; Deferoxamine; Drug Industry; Financial Support; Humans; Multicente

2004
Combined therapy with desferrioxamine and deferiprone: a new protocol for iron chelation in thalassemia.
    Journal of pediatric hematology/oncology, 2004, Volume: 26, Issue:7

    Topics: Adolescent; Adult; Alanine Transaminase; Child; Deferoxamine; Drug Therapy, Combination; Female; Fer

2004
Adherence to deferoxamine therapy: heeding Hippocrates and Osler.
    American journal of hematology, 2004, Volume: 76, Issue:4

    Topics: Adult; Child; Cross-Over Studies; Deferoxamine; Humans; Iron Chelating Agents; Iron Overload; Needle

2004
Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine.
    Haematologica, 2004, Volume: 89, Issue:10

    Topics: Adult; Age Factors; Arrhythmias, Cardiac; Blood Transfusion; Chelation Therapy; Cohort Studies; Defe

2004
Myocardial iron clearance during reversal of siderotic cardiomyopathy with intravenous desferrioxamine: a prospective study using T2* cardiovascular magnetic resonance.
    British journal of haematology, 2004, Volume: 127, Issue:3

    Topics: Adult; Cardiomyopathies; Case-Control Studies; Deferoxamine; Female; Humans; Infusions, Intravenous;

2004
Bone marrow transplantation in adults with thalassemia: Treatment and long-term follow-up.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Adolescent; Adult; Azathioprine; Bone Marrow Transplantation; Busulfan; Chelation Therapy; Clinical

2005
Effective new treatments of iron overload in thalassaemia using the ICOC combination therapy protocol of deferiprone (L1) and deferoxamine and of new chelating drugs.
    Haematologica, 2006, Volume: 91, Issue:6 Suppl

    Topics: Deferiprone; Deferoxamine; Drug Therapy, Combination; Humans; Iron Chelating Agents; Iron Overload;

2006
Low serum ferritin levels are misleading for detecting cardiac iron overload and increase the risk of cardiomyopathy in thalassemia patients. The importance of cardiac iron overload monitoring using magnetic resonance imaging T2 and T2*.
    Hemoglobin, 2006, Volume: 30, Issue:2

    Topics: Administration, Oral; Adult; Arrhythmias, Cardiac; Cardiomyopathies; Chelation Therapy; Combined Mod

2006
Thalassemia treatment and prevention in Uva Province, Sri Lanka: a public opinion survey.
    Hemoglobin, 2006, Volume: 30, Issue:2

    Topics: Abortion, Eugenic; Adolescent; Adult; Blood Transfusion; Chelation Therapy; Combined Modality Therap

2006
Survival of medically treated thalassemia patients in Cyprus. Trends and risk factors over the period 1980-2004.
    Haematologica, 2006, Volume: 91, Issue:9

    Topics: Cyprus; Deferiprone; Deferoxamine; Drug Therapy, Combination; Female; Humans; Iron Chelating Agents;

2006
Physical growth patterns and dental caries in thalassemia.
    Indian pediatrics, 2006, Volume: 43, Issue:12

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferiprone; Deferoxamine; Dental Caries; Female; Ferrit

2006
Clinical and economic burden of infused iron chelation therapy in the United States.
    Transfusion, 2007, Volume: 47, Issue:10

    Topics: Adolescent; Adult; Blood Transfusion; Child; Cohort Studies; Deferoxamine; Female; Ferritins; Humans

2007
Curcumin contributes to in vitro removal of non-transferrin bound iron by deferiprone and desferrioxamine in thalassemic plasma.
    Medicinal chemistry (Shariqah (United Arab Emirates)), 2007, Volume: 3, Issue:5

    Topics: Chromatography, High Pressure Liquid; Curcumin; Deferiprone; Deferoxamine; Humans; Iron; Iron Chelat

2007
Outcomes, utilization, and costs among thalassemia and sickle cell disease patients receiving deferoxamine therapy in the United States.
    American journal of hematology, 2008, Volume: 83, Issue:4

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Cardiomyopathies; Chelation Therapy; Child; Child, Preschool

2008
Transfusion-dependent thalassaemia: a new era.
    The Medical journal of Australia, 2008, Jan-21, Volume: 188, Issue:2

    Topics: Benzoates; Cardiomyopathies; Deferasirox; Deferiprone; Deferoxamine; Drug Prescriptions; Erythrocyte

2008
Management and clinical outcomes of transfusion-dependent thalassaemia major in an Australian tertiary referral clinic.
    The Medical journal of Australia, 2008, Jan-21, Volume: 188, Issue:2

    Topics: Adult; Age Factors; Australia; Cardiomyopathies; Deferiprone; Deferoxamine; Diabetes Mellitus; Drug

2008
Myocyte damage and loss of myofibers is the potential mechanism of iron overload toxicity in congestive cardiac failure in thalassemia. Complete reversal of the cardiomyopathy and normalization of iron load by deferiprone.
    Hemoglobin, 2008, Volume: 32, Issue:1-2

    Topics: Cardiomyopathies; Chelation Therapy; Deferiprone; Deferoxamine; Female; Ferritins; Humans; Iron; Iro

2008
Long term comparative studies in thalassemia patients treated with deferoxamine or a deferoxamine/deferiprone combination. Identification of effective chelation therapy protocols.
    Hemoglobin, 2008, Volume: 32, Issue:1-2

    Topics: Adult; Chelation Therapy; Clinical Protocols; Deferiprone; Deferoxamine; Drug Therapy, Combination;

2008
[Modern therapeutic possibilities in Cooley's disease].
    Atti della Accademia dei fisiocritici in Siena. Sezione medico-fisica, 1966, Volume: 15, Issue:2

    Topics: Adolescent; Antibody Formation; Azathioprine; Betamethasone; Blood Transfusion; Child; Child, Presch

1966
Thalassemia intermedia, with iron overload, cardiac failure, diabetes mellitus, hypopituitarism and porphyrinuria.
    The American journal of medicine, 1967, Volume: 42, Issue:3

    Topics: Adult; Blood Transfusion; Deferoxamine; Diabetes Mellitus; Folic Acid; Folic Acid Deficiency; Heart

1967
[Therapeutic results in the treatment of primary and secondary hemochromatoses with Desferal].
    Blut, 1967, Volume: 15, Issue:1

    Topics: Anemia, Macrocytic; Blood Transfusion; Deferoxamine; Hemochromatosis; Hemosiderosis; Humans; Injecti

1967
Radioactive iron (59Fe) excretion through the urine and feces after intravenous iron-59 administration in congenital hemolytic anemias.
    Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 1967, Volume: 8, Issue:5

    Topics: Anemia, Sickle Cell; Deferoxamine; Feces; Humans; Iron Isotopes; Thalassemia

1967
Iron chelation with oral desferrioxamine.
    Lancet (London, England), 1980, Sep-27, Volume: 2, Issue:8196

    Topics: Administration, Oral; Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Humans; Iron; Thalas

1980
Iron chelation in red cell ghosts.
    Lancet (London, England), 1981, Jan-24, Volume: 1, Issue:8213

    Topics: Blood Transfusion; Deferoxamine; Erythrocyte Membrane; Erythrocytes; Humans; Thalassemia

1981
Ocular toxicity of high-dose intravenous desferrioxamine.
    Lancet (London, England), 1983, Jul-23, Volume: 2, Issue:8343

    Topics: Adolescent; Adult; Cataract; Child; Child, Preschool; Dark Adaptation; Deferoxamine; Female; Follow-

1983
Rapid desensitisation for desferrioxamine anaphylactoid reaction.
    Lancet (London, England), 1983, Oct-08, Volume: 2, Issue:8354

    Topics: Adult; Anaphylaxis; Deferoxamine; Desensitization, Immunologic; Female; Humans; Thalassemia; Time Fa

1983
Desferrioxamine and systemic yersiniosis.
    Lancet (London, England), 1983, Dec-10, Volume: 2, Issue:8363

    Topics: Animals; Deferoxamine; Humans; Iron; Mice; Thalassemia; Yersinia enterocolitica; Yersinia Infections

1983
Yersinia pseudotuberculosis septicaemia in thalassaemia major.
    Lancet (London, England), 1984, Jan-07, Volume: 1, Issue:8367

    Topics: Adolescent; Deferoxamine; Female; Humans; Sepsis; Thalassemia; Yersinia Infections; Yersinia pseudot

1984
High-dose chelation therapy in thalassaemia.
    Lancet (London, England), 1984, Feb-18, Volume: 1, Issue:8373

    Topics: Deferoxamine; Heart; Humans; Iron; Liver; Thalassemia

1984
Desferrioxamine to improve cardiac function in iron-overloaded patients with thalassemia major.
    Lancet (London, England), 1984, Feb-18, Volume: 1, Issue:8373

    Topics: Deferoxamine; Heart Diseases; Humans; Iron; Thalassemia; Transfusion Reaction

1984
Visual loss in patient on high-dose subcutaneous desferrioxamine.
    Lancet (London, England), 1984, Mar-24, Volume: 1, Issue:8378

    Topics: Child; Deferoxamine; Female; Humans; Injections, Subcutaneous; Thalassemia; Vision Disorders

1984
Prophylaxis of systemic yersinosis in thalassaemia major.
    Lancet (London, England), 1984, Apr-07, Volume: 1, Issue:8380

    Topics: Child; Deferoxamine; Female; Humans; Risk; Sepsis; Thalassemia; Yersinia Infections

1984
[Thalassaemia intermedia. Clinical and laboratory study. Therapeutic suggestions (author's transl)].
    La Nouvelle presse medicale, 1982, Jan-30, Volume: 11, Issue:4

    Topics: Age Factors; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Female; Fetal Hemoglobin; Hem

1982
Beta thalassemia and heart disease: three decades of gradual progress.
    Transactions of the American Clinical and Climatological Association, 1985, Volume: 96

    Topics: Blood Transfusion; Cardiomegaly; Child; Deferoxamine; Erythrocyte Transfusion; Heart Diseases; Human

1985
[Iron overload in a beta thalassemia heterozygote of the intermediate type in a subject of Alsation origin. Results of iron chelation treatment].
    Nouvelle revue francaise d'hematologie, 1984, Volume: 26, Issue:5

    Topics: Anemia; Deferoxamine; Female; Ferritins; Hemosiderosis; Heterozygote; HLA Antigens; HLA-A3 Antigen;

1984
[Puberty-specific gonadotropin rhythm in girls with homozygous beta-thalassemia during continuous subcutaneous desferrioxamine infusions and a simultaneous blood transfusion regimen].
    Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1983, Volume: 131, Issue:1

    Topics: Adolescent; Blood Transfusion; Deferoxamine; Female; Follicle Stimulating Hormone; Humans; Infusions

1983
Successful pregnancy in beta-thalassaemia major.
    Australian paediatric journal, 1983, Volume: 19, Issue:3

    Topics: Adult; Blood Transfusion; Deferoxamine; Female; Glucose; Humans; Hypoglycemia; Infant, Newborn; Infa

1983
A study of the mechanisms and sites of action of desferrioxamine in thalassaemia major.
    Acta haematologica, 1984, Volume: 71, Issue:2

    Topics: Child; Deferoxamine; Erythrocytes; Feces; Humans; Injections, Subcutaneous; Iron; Iron Chelating Age

1984
Allergy to desferrioxamine.
    Journal of inherited metabolic disease, 1984, Volume: 7, Issue:3

    Topics: Child; Deferoxamine; Drug Hypersensitivity; Female; Humans; Thalassemia

1984
[Effect of hematologic treatment on the growth and puberty of children with thalassemia major].
    Archives francaises de pediatrie, 1984, Volume: 41, Issue:4

    Topics: Adolescent; Blood Transfusion; Body Height; Child; Combined Modality Therapy; Deferoxamine; Female;

1984
Depletion of excessive liver iron stores with desferrioxamine.
    British journal of haematology, 1984, Volume: 58, Issue:2

    Topics: Adolescent; Child; Deferoxamine; Humans; Iron; Liver; Thalassemia

1984
Porphyria cutanea tarda in beta-thalassemia trait carriers.
    Dermatologica, 1984, Volume: 169, Issue:3

    Topics: Adult; Deferoxamine; Heterozygote; Humans; Liver Diseases; Male; Middle Aged; Porphyrias; Skin Disea

1984
[Deferoxamine in hemosiderosis. Fecal iron excretion during continuous subcutaneous infusion].
    Deutsche medizinische Wochenschrift (1946), 1984, Nov-02, Volume: 109, Issue:44

    Topics: Adolescent; Child; Child, Preschool; Deferoxamine; Feces; Hemosiderosis; Humans; Injections, Subcuta

1984
Ocular changes in patients undergoing long-term desferrioxamine treatment.
    The British journal of ophthalmology, 1984, Volume: 68, Issue:12

    Topics: Adolescent; Adult; Child; Deferoxamine; Electrooculography; Electroretinography; Female; Glucose Tol

1984
Thalassemia.
    Advances in pediatrics, 1984, Volume: 31

    Topics: Blood Transfusion; Chromosome Deletion; Deferoxamine; DNA; Erythrocyte Transfusion; Female; Gene Exp

1984
A successful pregnancy outcome in transfusion dependent thalassaemia major.
    The Australian & New Zealand journal of obstetrics & gynaecology, 1984, Volume: 24, Issue:1

    Topics: Adult; Blood Transfusion; Deferoxamine; Erythrocyte Transfusion; Female; Humans; Infant, Newborn; Ma

1984
Early left ventricular dysfunction and chelation therapy in thalassemia major.
    Annals of internal medicine, 1983, Volume: 99, Issue:4

    Topics: Adolescent; Adult; Blood Transfusion; Child; Coronary Vessels; Deferoxamine; Ferritins; Heart Ventri

1983
[Desferrioxamine in thalassemia].
    Harefuah, 1983, May-15, Volume: 104, Issue:10

    Topics: Adolescent; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Female; Humans; Infusions, Par

1983
Management of thalassaemia major.
    Archives of disease in childhood, 1983, Volume: 58, Issue:12

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Diagnosis, Differential

1983
Management of thalassaemia major.
    Archives of disease in childhood, 1983, Volume: 58, Issue:12

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Diagnosis, Differential

1983
Management of thalassaemia major.
    Archives of disease in childhood, 1983, Volume: 58, Issue:12

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Diagnosis, Differential

1983
Management of thalassaemia major.
    Archives of disease in childhood, 1983, Volume: 58, Issue:12

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Diagnosis, Differential

1983
[Our experience in the treatment of malleolar ulcers in thalassemia].
    Minerva medica, 1983, May-12, Volume: 74, Issue:20

    Topics: Adolescent; Adult; Bandages; Blood Transfusion; Deferoxamine; Female; Humans; Leg Ulcer; Pentoxifyll

1983
Use of the one sample t-test in the real world.
    Journal of chronic diseases, 1984, Volume: 37, Issue:2

    Topics: Deferoxamine; Ferritins; Humans; Research; Statistics as Topic; Thalassemia

1984
Iron absorption in non-transfused iron loading anaemias: prediction of risk for iron loading, and response to iron chelation treatment, in beta thalassaemia intermedia and congenital sideroblastic anaemias.
    Haematologia, 1984, Volume: 17, Issue:1

    Topics: Absorption; Administration, Oral; Age Factors; Anemia, Sideroblastic; Chelating Agents; Deferoxamine

1984
The simple rubber band technic for slow subcutaneous infusion of desferrioxamine.
    Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1984, Volume: 67, Issue:2

    Topics: Child; Deferoxamine; Humans; Infusions, Parenteral; Iron; Male; Methods; Thalassemia

1984
Pituitary-thyroid function in children with beta-thalassaemia major.
    Acta endocrinologica, 1981, Volume: 96, Issue:1

    Topics: Adolescent; Blood Transfusion; Child; Deferoxamine; Female; Humans; Male; Pituitary Gland, Anterior;

1981
Desferrioxamine-induced iron outputs in Cooley's anemia. Results and perspectives.
    Haematologica, 1981, Volume: 66, Issue:2

    Topics: Adolescent; Ascorbic Acid; Blood Transfusion; Child; Deferoxamine; Female; Humans; Iron; Male; Splen

1981
Delayed decrease in serum ferritin in polytransfused children with thalassemia major after continuous subcutaneous infusions of desferrioxamine.
    Acta haematologica, 1981, Volume: 66, Issue:2

    Topics: Blood Transfusion; Child; Child, Preschool; Deferoxamine; Ferritins; Humans; Infusions, Parenteral;

1981
Iron chelation in transfusion-dependent thalassemia with chronic hepatitis.
    Acta haematologica, 1982, Volume: 67, Issue:1

    Topics: Adolescent; Alanine Transaminase; Child; Child, Preschool; Chronic Disease; Deferoxamine; Female; Fe

1982
Survival and desferrioxamine in thalassaemia major.
    British medical journal (Clinical research ed.), 1982, May-08, Volume: 284, Issue:6326

    Topics: Adult; Ascorbic Acid; Deferoxamine; Humans; Iron; Thalassemia

1982
Intensive iron chelation therapy in beta-thalassemia major: some effects on iron metabolism and blood transfusion dependence.
    Acta haematologica, 1982, Volume: 68, Issue:2

    Topics: Adolescent; Adult; Aging; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Feces; Female; F

1982
The management of the improved prognosis in thalassemia major.
    Birth defects original article series, 1982, Volume: 18, Issue:7

    Topics: Adolescent; Adult; Attitude to Death; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Empl

1982
Subcutaneous desferrioxamine: the effect of three years' treatment on liver, iron, serum ferritin, and comments on echocardiography.
    Birth defects original article series, 1982, Volume: 18, Issue:7

    Topics: Adolescent; Ascorbic Acid Deficiency; Aspartate Aminotransferases; Child; Deferoxamine; Echocardiogr

1982
Therapy of HBsAg-negative chronic active hepatitis in transfusion-dependent thalassemia major.
    Birth defects original article series, 1982, Volume: 18, Issue:7

    Topics: Aspartate Aminotransferases; Child; Child, Preschool; Deferoxamine; Hepatitis B; Hepatitis B Surface

1982
Editorial retrospective. Iron loading in thalassemia--five years with the pump.
    The New England journal of medicine, 1983, Feb-24, Volume: 308, Issue:8

    Topics: Adolescent; Adult; Child; Deferoxamine; Humans; Iron; Thalassemia; Transfusion Reaction

1983
Pancreatic sonography in thalassemia major.
    Klinische Padiatrie, 1983, Volume: 195, Issue:2

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Hemosiderosis; Humans; Pancreatic Disease

1983
Effect of subcutaneous desferrioxamine on iron balance in young thalassemia major patients.
    The American journal of pediatric hematology/oncology, 1983,Spring, Volume: 5, Issue:1

    Topics: Age Factors; Child, Preschool; Deferoxamine; Dose-Response Relationship, Drug; Humans; Infant; Infus

1983
The management of iron chelation therapy.
    British journal of haematology, 1983, Volume: 54, Issue:4

    Topics: Anemia, Hemolytic, Congenital; Ascorbic Acid; Child; Child, Preschool; Deferoxamine; Drug Administra

1983
Iron overload: pathogenesis and treatment with chelating agents.
    Blut, 1983, Volume: 47, Issue:2

    Topics: Blood Transfusion; Bloodletting; Chelating Agents; Deferoxamine; Hemochromatosis; Humans; Infusions,

1983
[Obstetrical and hematological problems in a pregnant woman with intermediate beta-thalassemia].
    Minerva ginecologica, 1983, Volume: 35, Issue:4

    Topics: Adult; Blood Transfusion; Deferoxamine; Female; Humans; Pregnancy; Pregnancy Complications, Hematolo

1983
Thalassemia.
    Progress in clinical and biological research, 1983, Volume: 127

    Topics: Chelating Agents; Costs and Cost Analysis; Deferoxamine; Humans; Iron; Thalassemia; Transfusion Reac

1983
Current concepts in the overall management of thalassemia.
    Annals of the New York Academy of Sciences, 1980, Volume: 344

    Topics: Biological Transport; Blood Transfusion; Chelating Agents; Deferoxamine; Erythrocyte Transfusion; Ex

1980
Evaluation of cardiac function in patients with thalassemia major.
    Annals of the New York Academy of Sciences, 1980, Volume: 344

    Topics: Adolescent; Adult; Ascorbic Acid; Child; Child, Preschool; Deferoxamine; Heart; Heart Diseases; Hear

1980
Clinical management of thalassemia. Decreasing iron stores during intensive chelation therapy.
    Annals of the New York Academy of Sciences, 1980, Volume: 344

    Topics: Ascorbic Acid; Blood Transfusion; Child; Deferoxamine; Erythrocyte Transfusion; Humans; Iron; Male;

1980
Chelation therapy, transfusion requirement, and iron balance in young thalassemic patients.
    Annals of the New York Academy of Sciences, 1980, Volume: 344

    Topics: Adolescent; Ascorbic Acid; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Erythrocyte Tra

1980
Combined vitamin D parathyroid defect in thalassemia major.
    Archives of internal medicine, 1982, Volume: 142, Issue:4

    Topics: 25-Hydroxyvitamin D 2; Adolescent; Adult; Child; Deferoxamine; Ergocalciferols; Female; Humans; Hypo

1982
Zinc deficiency developing in treatment for thalassaemia.
    Journal of the Royal Society of Medicine, 1982, Volume: 75, Issue:1

    Topics: Child; Deferoxamine; Humans; Male; Pentetic Acid; Thalassemia; Transfusion Reaction; Zinc

1982
[Continuous subcutaneous desferrioxamine infusions in patients with hemosiderosis (author's transl)].
    Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1982, Volume: 130, Issue:3

    Topics: Adolescent; Adult; Anemia, Aplastic; Child; Child, Preschool; Deferoxamine; Hemosiderosis; Humans; I

1982
Ferrioxamine excretion in iron-loaded man.
    Blood, 1982, Volume: 60, Issue:2

    Topics: Adult; Ascorbic Acid; Deferoxamine; Dose-Response Relationship, Drug; Feces; Hemosiderosis; Humans;

1982
[Thalassemic cardiopathy: serial echocardiographic evaluation].
    Giornale di clinica medica, 1982, Volume: 63, Issue:4

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Echocardiography; Female; Ferritins; Heart

1982
Reduction of iron overload in thalassemia.
    Birth defects original article series, 1982, Volume: 18, Issue:7

    Topics: Adolescent; Adult; Aging; Animals; Cell Separation; Child; Child, Preschool; Deferoxamine; Erythrocy

1982
[Monitoring and appraisal of the effects of blood transfusion and iron chelation in thalassemia major].
    Nouvelle revue francaise d'hematologie, 1982, Volume: 24, Issue:5

    Topics: Adolescent; Adult; Blood Group Incompatibility; Child; Child Development; Child, Preschool; Deferoxa

1982
Early iron overload in beta-thalassaemia major: when to start chelation therapy?
    Archives of disease in childhood, 1982, Volume: 57, Issue:12

    Topics: Child, Preschool; Deferoxamine; Hemochromatosis; Humans; Infant; Iron; Thalassemia; Transfusion Reac

1982
Chelation therapy in iron poisoning.
    Journal of toxicology. Clinical toxicology, 1982, Volume: 19, Issue:8

    Topics: Animals; Deferoxamine; Dogs; Drug Administration Schedule; Humans; Infusions, Parenteral; Injections

1982
Chelation therapy for iron overload.
    Nutrition reviews, 1980, Volume: 38, Issue:5

    Topics: Animals; Chelating Agents; Deferoxamine; Hemochromatosis; Hemosiderosis; Humans; Rats; Thalassemia

1980
Response to long-term deferoxamine therapy in thalassemia.
    The Journal of pediatrics, 1981, Volume: 99, Issue:5

    Topics: Adolescent; Child; Deferoxamine; Ferritins; Humans; Iron; Liver Function Tests; Male; Thalassemia; T

1981
Chelation therapy in beta-thalassemia major. III. The role of splenectomy in achieving iron balance.
    The Journal of pediatrics, 1981, Volume: 99, Issue:5

    Topics: Adolescent; Adult; Age Factors; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Humans; In

1981
Iron overload and desferrioxamine chelation therapy in beta-thalassemia intermedia.
    European journal of pediatrics, 1981, Volume: 137, Issue:3

    Topics: Adolescent; Age Factors; Child; Child, Preschool; Deferoxamine; Female; Ferritins; Humans; Infant; I

1981
Intravenous and subcutaneous desferrioxamine therapy in children with severe iron overload.
    European journal of pediatrics, 1981, Volume: 137, Issue:3

    Topics: Adolescent; Anemia, Aplastic; Anemia, Sideroblastic; Child; Child, Preschool; Deferoxamine; Hemoside

1981
Tinnitus in a patient with beta-thalassaemia intermedia on long-term treatment with desferrioxamine.
    Postgraduate medical journal, 1981, Volume: 57, Issue:671

    Topics: Adult; Deferoxamine; Female; Humans; Iron; Thalassemia; Time Factors; Tinnitus

1981
[Monitoring of the harmful effects of iron on the hearts of patients with beta-thalassemia major, using non-invasive cardiological technics].
    Bollettino della Societa italiana di cardiologia, 1981, Volume: 26, Issue:10

    Topics: Adolescent; Adult; Cardiomyopathies; Child; Child, Preschool; Deferoxamine; Echocardiography; Electr

1981
Depressed serum somatomedin activity in beta-thalassemia.
    The Journal of pediatrics, 1980, Volume: 96, Issue:2

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Female; Growth Disorders; Hemosiderosis; H

1980
Advances in the management of homozygous beta-thalassaemia, including desferrioxamine infusion therapy and prenatal diagnosis.
    Paediatrician, 1980, Volume: 9, Issue:2

    Topics: Blood Transfusion; Deferoxamine; Female; Fetal Blood; Fetal Diseases; Globins; Humans; Pregnancy; Pr

1980
[Treatment of iron overload due to repeated transfusions with subcutaneous infusions of desferrioxamine (author's transl)].
    Archives francaises de pediatrie, 1980, Volume: 37, Issue:4

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Female; Ferritins; Hemosiderosis; Humans;

1980
Treatment of iron storage disorders.
    Drugs, 1980, Volume: 20, Issue:3

    Topics: Anemia; Deferoxamine; Hemochromatosis; Humans; Iron; Liver Cirrhosis; Porphyrias; Skin Diseases; Tha

1980
Successful pregnancy in transfusion-dependent thalassaemia.
    Archives of disease in childhood, 1980, Volume: 55, Issue:7

    Topics: Adult; Blood Transfusion; Deferoxamine; Female; Humans; Infant, Newborn; Pregnancy; Pregnancy Compli

1980
Vitamin C and iron.
    The New England journal of medicine, 1981, Jan-15, Volume: 304, Issue:3

    Topics: Administration, Oral; Adult; Animals; Ascorbic Acid; Ascorbic Acid Deficiency; Deferoxamine; Female;

1981
[Echocardiographic measurements in transfused thalassemic major children].
    Minerva pediatrica, 1980, May-15, Volume: 32, Issue:9

    Topics: Blood Transfusion; Child; Child, Preschool; Deferoxamine; Echocardiography; Female; Ferritins; Hemog

1980
[Role and therapeutic use of deferoxamine in iron overload due to thalassemia (author's transl)].
    Archives francaises de pediatrie, 1980, Volume: 37, Issue:5

    Topics: Adolescent; Child; Child, Preschool; Deferoxamine; Female; Humans; Iron; Male; Thalassemia

1980
Desferrioxamine therapy accelerates clearance of iron deposits after bone marrow transplantation for thalassaemia.
    British journal of haematology, 1995, Volume: 89, Issue:4

    Topics: Adolescent; Biopsy; Bone Marrow Transplantation; Child; Deferoxamine; Female; Ferritins; Humans; Iro

1995
Autoantibodies in thalassaemia major: relationship with oral iron chelator L1.
    The Journal of the Association of Physicians of India, 1993, Volume: 41, Issue:6

    Topics: Adolescent; Adult; Antibodies, Antinuclear; Autoimmune Diseases; Blood Transfusion; Child; Deferipro

1993
Zinc concentration in patients with iron overload receiving oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one or desferrioxamine.
    Journal of clinical pathology, 1994, Volume: 47, Issue:7

    Topics: Adolescent; Adult; Blood Glucose; Deferiprone; Deferoxamine; Diabetes Mellitus; Female; Glucose Tole

1994
Development of oral iron chelator L1.
    Lancet (London, England), 1993, Apr-24, Volume: 341, Issue:8852

    Topics: Agranulocytosis; Deferiprone; Deferoxamine; Humans; Iron Chelating Agents; Pyridones; Thalassemia

1993
Could chelation therapy with deferoxamine enhance the percentage of responders to interferon therapy in chronic hepatitis C?
    Acta haematologica, 1993, Volume: 90, Issue:4

    Topics: Chelation Therapy; Chronic Disease; Combined Modality Therapy; Deferoxamine; Drug Synergism; Ferriti

1993
Differential toxicity of alpha-keto hydroxypyridine iron chelators and desferrioxamine to human haemopoietic precursors in vitro.
    European journal of haematology, 1994, Volume: 52, Issue:3

    Topics: Bone Marrow Cells; Cell Division; Deferiprone; Deferoxamine; Hematopoiesis; Humans; In Vitro Techniq

1994
Liver iron overload and liver fibrosis in thalassemia.
    Bone marrow transplantation, 1993, Volume: 12 Suppl 1

    Topics: Adolescent; Adult; Chelation Therapy; Child; Child, Preschool; Combined Modality Therapy; Deferoxami

1993
[Long-term efficacy of subcutaneous administration of deferoxamine in patients with secondary hemochromatosis].
    [Rinsho ketsueki] The Japanese journal of clinical hematology, 1996, Volume: 37, Issue:4

    Topics: Aged; Anemia, Aplastic; Deferoxamine; Female; Hemochromatosis; Humans; Injections, Subcutaneous; Mal

1996
[Thalassemia today].
    Schweizerische medizinische Wochenschrift, 1996, Nov-02, Volume: 126, Issue:44

    Topics: Adolescent; Adult; Child; Comorbidity; Deferoxamine; Humans; Life Expectancy; Patient Compliance; Qu

1996
Laboratory evaluation of a new delivery system to improve patient compliance with chelation therapy.
    Clinical and laboratory haematology, 1996, Volume: 18, Issue:1

    Topics: Adolescent; Adult; Chelation Therapy; Deferoxamine; Drug Delivery Systems; Humans; Infusions, Intrav

1996
The effectiveness of deferiprone in thalassemia.
    Blood, 1997, Jul-15, Volume: 90, Issue:2

    Topics: Deferiprone; Deferoxamine; Humans; Iron; Iron Chelating Agents; Pyridones; Thalassemia

1997
[Intensive intravenous chelation in thalassemic patients with iron overload].
    Minerva pediatrica, 1998, Volume: 50, Issue:3

    Topics: Adolescent; Adult; Chelation Therapy; Deferoxamine; Echocardiography; Humans; Infusions, Intravenous

1998
Serum ferritin, desferrioxamine, and evolution of HIV-1 infection in thalassemic patients.
    Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association, 1998, Aug-15, Volume: 18, Issue:5

    Topics: Child; Cohort Studies; Confounding Factors, Epidemiologic; Deferoxamine; Disease Progression; Dose-R

1998
Microstructural analysis of severe bone lesions in seven thalassemic patients treated with deferoxamine.
    Calcified tissue international, 2000, Volume: 67, Issue:2

    Topics: Adolescent; Apatites; Biopsy; Bone and Bones; Chelating Agents; Child; Deferoxamine; Female; Humans;

2000
Osteochondrodystrophic lesions in chelated thalassemic patients: an histological analysis.
    Calcified tissue international, 2000, Volume: 67, Issue:2

    Topics: Adolescent; Biopsy; Bone Diseases; Cartilage; Chelating Agents; Child; Deferoxamine; Female; Fractur

2000
Pregnancy outcome of a transfusion-dependent thalassemic woman.
    Annals of hematology, 2000, Volume: 79, Issue:10

    Topics: Blood Transfusion; Chelating Agents; Deferoxamine; Female; Ferritins; Humans; Pregnancy; Pregnancy C

2000
Persistence of delayed adrenarche in boys with thalassemia.
    Journal of pediatric endocrinology & metabolism : JPEM, 2001, Volume: 14, Issue:4

    Topics: Adolescent; Age Determination by Skeleton; Blood Transfusion; Body Height; Body Mass Index; Bone Den

2001
Determination of a new oral iron chelator, ICL670, and its iron complex in plasma by high-performance liquid chromatography and ultraviolet detection.
    Journal of chromatography. B, Biomedical sciences and applications, 2001, May-05, Volume: 755, Issue:1-2

    Topics: Benzoates; Calibration; Chromatography, High Pressure Liquid; Deferasirox; Deferiprone; Deferoxamine

2001
[Pregnancy in women with thalassaemia].
    Minerva ginecologica, 2001, Volume: 53, Issue:3

    Topics: Adult; Blood Transfusion; Chelating Agents; Deferoxamine; Female; Folic Acid; Hematinics; Humans; In

2001
Variations of ferritin levels over a period of 15 years as a compliance chelation index in thalassemic patients.
    American journal of hematology, 2001, Volume: 68, Issue:4

    Topics: Adolescent; Adult; Chelation Therapy; Child; Child, Preschool; Deferoxamine; Drug Monitoring; Ferrit

2001
Long-term administration of high-dose deferoxamine 2 days per week in thalassemic patients.
    European journal of haematology, 2001, Volume: 67, Issue:4

    Topics: Adult; Chelating Agents; Chelation Therapy; Deferoxamine; Female; Ferritins; Humans; Infusion Pumps;

2001
Reversibility of cirrhosis in patients cured of thalassemia by bone marrow transplantation.
    Annals of internal medicine, 2002, May-07, Volume: 136, Issue:9

    Topics: Adolescent; Adult; Antiviral Agents; Biopsy; Bone Marrow Transplantation; Child; Combined Modality T

2002
Summaries for patients. Reversibility of liver scarring in patients who are cured of thalassemia.
    Annals of internal medicine, 2002, May-07, Volume: 136, Issue:9

    Topics: Adolescent; Adult; Antiviral Agents; Bone Marrow Transplantation; Child; Combined Modality Therapy;

2002
Effect of dose, time, and ascorbate on iron excretion after subcutaneous desferrioxamine.
    Lancet (London, England), 1977, May-07, Volume: 1, Issue:8019

    Topics: Administration, Oral; Adolescent; Adult; Anemia, Sideroblastic; Ascorbic Acid; Child; Deferoxamine;

1977
Chelation regimens with desferrioxamine.
    Lancet (London, England), 1977, May-21, Volume: 1, Issue:8021

    Topics: Deferoxamine; Dose-Response Relationship, Drug; Infusions, Parenteral; Thalassemia

1977
Iron absorption in iron-loading anaemias: Effect of subcutaneous desferrioxamine infusions.
    Lancet (London, England), 1977, Oct-08, Volume: 2, Issue:8041

    Topics: Administration, Oral; Adolescent; Adult; Anemia, Aplastic; Anemia, Sideroblastic; Ascorbic Acid; Bin

1977
Iron absorption in iron-loading anaemias.
    Lancet (London, England), 1977, Oct-29, Volume: 2, Issue:8044

    Topics: Deferoxamine; Humans; Intestinal Absorption; Iron; Thalassemia

1977
Prevention of iron loading in transfusion-dependent thalassaemia.
    Lancet (London, England), 1978, Jun-03, Volume: 1, Issue:8075

    Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Deferoxamine; Dose-Response Relationship, D

1978
Subcutaneous desferrioxamine in homozygous beta-thalassaemia.
    Lancet (London, England), 1978, Nov-25, Volume: 2, Issue:8100

    Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Deferoxamine; Hemosiderosis; Homozygote; Hu

1978
Improvement in iron status and liver function in patients with transfusional iron overload with long-term subcutaneous desferrioxamine.
    Lancet (London, England), 1979, May-05, Volume: 1, Issue:8123

    Topics: Adolescent; Adult; Aged; Anemia, Aplastic; Anemia, Sideroblastic; Aspartate Aminotransferases; Child

1979
Correlation between computed tomographic values and liver iron content in thalassaemia major with iron overload.
    Lancet (London, England), 1979, Jun-23, Volume: 1, Issue:8130

    Topics: Adolescent; Biopsy; Blood Transfusion; Child; Deferoxamine; Female; Humans; Iron; Liver; Male; Thala

1979
Rhodotorulic acid--investigation of its potential as an iron-chelating drug.
    The Journal of pharmacology and experimental therapeutics, 1979, Volume: 209, Issue:3

    Topics: Adult; Animals; Deferoxamine; Dogs; Female; Haplorhini; Humans; Hydroxamic Acids; Hydroxybenzoates;

1979
The clinical management of homozygous beta-thalassemia.
    Haematologica, 1979, Volume: 64, Issue:1

    Topics: Blood Transfusion; Deferoxamine; Endocrine System Diseases; Growth Disorders; Humans; Splenectomy; T

1979
Impaired parathyroid response to induced hypocalcemia in thalassemia major.
    The Journal of pediatrics, 1979, Volume: 95, Issue:2

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Edetic Acid; Ferritins; Humans; Hypocalce

1979
Drugs in current use: thalassaemia.
    The Australian nurses' journal. Royal Australian Nursing Federation, 1978, Volume: 8, Issue:3

    Topics: Deferoxamine; Humans; Thalassemia

1978
Acute renal insufficiency occurring during intravenous desferrioxamine therapy.
    Scandinavian journal of haematology, 1979, Volume: 22, Issue:3

    Topics: Acute Kidney Injury; Adolescent; Deferoxamine; Hemosiderosis; Humans; Injections, Intravenous; Male;

1979
Pharmacist involvement in a deferoxamine education program for patients with Cooley's anemia.
    American journal of hospital pharmacy, 1979, Volume: 36, Issue:6

    Topics: Ascorbic Acid; Asepsis; Deferoxamine; Drug Therapy, Combination; Evaluation Studies as Topic; Humans

1979
Mechanism of desferrioxamine-induced iron excretion in thalassaemia.
    British journal of haematology, 1979, Volume: 42, Issue:1

    Topics: Adolescent; Adult; Child; Child, Preschool; Cholecystectomy; Deferoxamine; Humans; Iron; Iron Chelat

1979
[Experience with desferrioxamine treatment by slow subcutaneous administration, in thalassemia].
    Minerva pediatrica, 1979, May-31, Volume: 31, Issue:10

    Topics: Adolescent; Adult; Child; Deferoxamine; Female; Humans; Injections, Intramuscular; Male; Siderosis;

1979
[Experience with desferrioxamine treatment by intravenous administration, in thalassemia].
    Minerva pediatrica, 1979, May-31, Volume: 31, Issue:10

    Topics: Child; Deferoxamine; Female; Humans; Infusions, Parenteral; Male; Siderosis; Thalassemia; Transfusio

1979
Studies in desferrioxamine and ferrioxamine metabolism in normal and iron-loaded subjects.
    British journal of haematology, 1979, Volume: 42, Issue:4

    Topics: Blood Transfusion; Deferoxamine; Ferric Compounds; Humans; Iron; Iron Chelating Agents; Thalassemia;

1979
Increased risk of diabetes mellitus in beta- thalassemia major due to iron overload.
    Helvetica paediatrica acta, 1979, Volume: 34, Issue:3

    Topics: Adolescent; Arginine; Blood Glucose; Child; Child, Preschool; Deferoxamine; Diabetes Mellitus, Type

1979
[Therapy of thalassemias].
    Monatsschrift fur Kinderheilkunde, 1979, Volume: 127, Issue:12

    Topics: Ascorbic Acid; Blood Transfusion; Deferoxamine; Humans; Splenectomy; Thalassemia

1979
Chelation therapy and ferritin levels in patients with homozygous beta-thalassemia.
    Progress in clinical and biological research, 1979, Volume: 34

    Topics: Adolescent; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Ferritins; Humans; Infant; Iro

1979
Iron loading and thalassemia--experimental successes and practical realities.
    The New England journal of medicine, 1977, Aug-25, Volume: 297, Issue:8

    Topics: Child; Deferoxamine; Humans; Injections, Intramuscular; Injections, Subcutaneous; Iron; Thalassemia;

1977
Evaluation of continuous desferrioxamine administration in adults with transfusional hemosiderosis.
    Transactions of the Association of American Physicians, 1977, Volume: 90

    Topics: Adult; Anemia, Sideroblastic; Ascorbic Acid; Deferoxamine; Drug Administration Schedule; Female; Hem

1977
Cardiac arrhythmias in thalassaemia major: evaluation of chelation treatment using ambulatory monitoring.
    British medical journal, 1978, Feb-11, Volume: 1, Issue:6109

    Topics: Adolescent; Adult; Ambulatory Care; Arrhythmias, Cardiac; Child; Deferoxamine; Humans; Monitoring, P

1978
Iron burden in sickle cell anemia.
    The Journal of pediatrics, 1978, Volume: 92, Issue:4

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Body Burden; Child; Child, Preschool; Deferoxamine; Ferritin

1978
Iron chelation therapy with deferoxamine in Cooley anemia.
    The Journal of pediatrics, 1978, Volume: 92, Issue:4

    Topics: Adolescent; Adult; Ascorbic Acid; Child; Child, Preschool; Deferoxamine; Female; Humans; Infusions,

1978
Cooley anemia: high transfusion regimen and chelation therapy, results, and perspective.
    The Journal of pediatrics, 1978, Volume: 92, Issue:4

    Topics: Adolescent; Ascorbic Acid; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Erythrocyte Tra

1978
[Further experiences with iron-chelating therapy (desferrioxamine and ascorbic acid) in siderochromatosis and Cooley's disease].
    Minerva medica, 1978, Mar-17, Volume: 69, Issue:13

    Topics: Adolescent; Adult; Aged; Ascorbic Acid; Deferoxamine; Drug Evaluation; Female; Hemochromatosis; Hemo

1978
Chronic iron overload: new chelators and new strategies.
    The Journal of laboratory and clinical medicine, 1978, Volume: 92, Issue:2

    Topics: Anemia, Sideroblastic; Animals; Ascorbic Acid; Chelating Agents; Deferoxamine; Hemosiderosis; Humans

1978
[Changes in urinary iron in thalassemia major in relation to the administration of desferrioxamine].
    La Pediatria, 1978, Mar-31, Volume: 86, Issue:1

    Topics: Child; Child, Preschool; Deferoxamine; Hemosiderosis; Humans; Infant; Iron; Thalassemia

1978
Intensive iron-chelation in thalassaemia.
    British medical journal, 1978, Sep-16, Volume: 2, Issue:6140

    Topics: Child; Child, Preschool; Deferoxamine; Humans; Infusions, Parenteral; Iron; Thalassemia; Transfusion

1978
Intensive iron-chelation in thalassaemia.
    British medical journal, 1978, Nov-18, Volume: 2, Issue:6149

    Topics: Adolescent; Child; Child, Preschool; Deferoxamine; Female; Humans; Infant; Injections, Subcutaneous;

1978
Iron chelation in thalassemia: mechanism of desferrioxamine action.
    Israel journal of medical sciences, 1978, Volume: 14, Issue:11

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Ferritins; Humans; Iron; Liver; Spleen; Th

1978
Treatment of primary hemochromatosis with deferoxamine.
    JAMA, 1979, Mar-16, Volume: 241, Issue:11

    Topics: Adult; Arrhythmias, Cardiac; Deferoxamine; Female; Heart Failure; Hemochromatosis; Humans; Male; Ped

1979
Pathogenesis and management of iron overload in thalassemia.
    Haematologica, 1975, Volume: 60, Issue:2

    Topics: Deferoxamine; Hemochromatosis; Humans; Iron; Pentetic Acid; Thalassemia

1975
Total management of thalassaemia major.
    Archives of disease in childhood, 1977, Volume: 52, Issue:6

    Topics: Adolescent; Adult; Ascorbic Acid; Child; Child, Preschool; Deferoxamine; Humans; Hypersplenism; Infa

1977
Continuous subcutaneous administration of deferoxamine in patients with iron overload.
    The New England journal of medicine, 1977, 08-25, Volume: 297, Issue:8

    Topics: Administration, Oral; Adolescent; Adult; Aged; Ascorbic Acid; Child; Child, Preschool; Deferoxamine;

1977
The inhibitory effect of vitamin E on desferrioxamine-induced iron excretion in rats.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1976, Volume: 152, Issue:2

    Topics: Animals; Deferoxamine; Female; Ferritins; Iron; Liver; Rats; Spleen; Thalassemia; Vitamin E

1976
Chelate mediated transfer of iron from transferrin to desferrioxamine.
    British journal of haematology, 1976, Volume: 34, Issue:2

    Topics: Chelating Agents; Deferoxamine; Humans; Iron; Thalassemia; Transferrin

1976
The thalassaemias.
    The Medical journal of Australia, 1976, Jul-03, Volume: 2, Issue:1

    Topics: Adolescent; Blood Transfusion; Child, Preschool; Deferoxamine; Humans; Infant; Mass Screening; Prena

1976
Practical approaches to the control of thalassaemia.
    Postgraduate medical journal, 1976, Volume: 52 Suppl 2

    Topics: Blood Transfusion; Deferoxamine; Female; Genetic Counseling; Humans; Male; Pregnancy; Prenatal Diagn

1976
The management of thalassemia major.
    Seminars in hematology, 1975, Volume: 12, Issue:3

    Topics: Adolescent; Adult; Blood Transfusion; Chelating Agents; Child; Child, Preschool; Deferoxamine; Diet

1975
Transfusional iron overload: the relationship between tissue iron concentration and hepatic fibrosis in thalassaemia.
    The Journal of pathology, 1975, Volume: 116, Issue:2

    Topics: Adolescent; Adult; Age Factors; Biopsy; Child; Child, Preschool; Deferoxamine; Humans; Iron; Iron Ch

1975
Reassessment of the use of desferrioxamine B in iron overload.
    The New England journal of medicine, 1976, Jun-24, Volume: 294, Issue:26

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Depression, Chemical; Humans; Infusions, P

1976
Desferrioxamine in acute iron poisoning.
    Lancet (London, England), 1992, Jun-27, Volume: 339, Issue:8809

    Topics: Child; Deferoxamine; Humans; Infusions, Intravenous; Iron; Respiratory Distress Syndrome; Thalassemi

1992
Reduction in tissue iron stores with a new regimen of continuous ambulatory intravenous deferoxamine.
    American journal of hematology, 1992, Volume: 41, Issue:1

    Topics: Adolescent; Adult; Ambulatory Care; Deferoxamine; Ferritins; Humans; Infusions, Intravenous; Injecti

1992
Growth plate injury of the long bones in treated beta-thalassemia.
    Skeletal radiology, 1992, Volume: 21, Issue:1

    Topics: Adolescent; Chelation Therapy; Child; Child, Preschool; Deferoxamine; Female; Follow-Up Studies; Gro

1992
Growth failure and bony changes induced by deferoxamine.
    The American journal of pediatric hematology/oncology, 1992,Spring, Volume: 14, Issue:1

    Topics: Alkaline Phosphatase; Body Height; Bone Development; Child, Preschool; Deferoxamine; Growth Plate; H

1992
Deferoxamine increases the susceptibility of beta-thalassemic, iron-overloaded mice to infection with Listeria monocytogenes.
    Life sciences, 1992, Volume: 50, Issue:18

    Topics: Animals; Colony Count, Microbial; Deferoxamine; Disease Susceptibility; Female; Injections, Intraper

1992
Bone density, mineral content, and cortical index in patients with thalassemia major and the correlation to their bone fractures, blood transfusions, and treatment with desferrioxamine.
    Calcified tissue international, 1992, Volume: 50, Issue:5

    Topics: Adolescent; Adult; Blood Transfusion; Bone and Bones; Bone Density; Child; Deferoxamine; Female; Fra

1992
[Intensifying iron chelating therapy with desferrioxamine using implantable venous access catheters (Port-A-Cath)].
    Archives francaises de pediatrie, 1992, Volume: 49, Issue:3

    Topics: Acute-Phase Reaction; Adolescent; Adult; Catheters, Indwelling; Deferoxamine; Female; Heart Failure;

1992
Neurophysiological and neuro-otological study of homozygous beta-thalassemia under long-term desferrioxamine (DFO) treatment.
    Acta neurologica Scandinavica, 1991, Volume: 83, Issue:5

    Topics: Adult; Audiometry, Pure-Tone; Auditory Threshold; Blood Transfusion; Brain Stem; Deferoxamine; Elect

1991
[Nursing and psychosocial care of patients with homozygote beta-thalassemia].
    Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege, 1991, Volume: 10, Issue:11

    Topics: Deferoxamine; Humans; Iron; Patient Compliance; Social Support; Thalassemia

1991
The effects of subcutaneous deferoxamine administration on renal function in thalassemia major.
    International journal of hematology, 1991, Volume: 54, Issue:5

    Topics: Adolescent; Adult; Child; Deferoxamine; Female; Glomerular Filtration Rate; Humans; Injections, Subc

1991
Iron chelation.
    The Journal of the Association of Physicians of India, 1991, Volume: 39, Issue:9

    Topics: Chelation Therapy; Deferiprone; Deferoxamine; Hemochromatosis; Humans; Iron; Iron Chelating Agents;

1991
Scoliosis in beta thalassemia.
    Pediatrics, 1991, Volume: 88, Issue:2

    Topics: Age Determination by Skeleton; Blood Transfusion; Child; Deferoxamine; Female; Ferritins; Humans; Ma

1991
Yersinia enterocolitica infection with ileal perforation associated with iron overload and deferoxamine therapy.
    Digestive diseases and sciences, 1991, Volume: 36, Issue:8

    Topics: Adolescent; Blood Transfusion; Deferoxamine; Humans; Ileal Diseases; Intestinal Perforation; Iron; L

1991
Systemic Yersinia enterocolitica infection associated with iron overload and deferoxamine therapy.
    AJR. American journal of roentgenology, 1991, Volume: 157, Issue:4

    Topics: Blood Transfusion; Child, Preschool; Deferoxamine; Gastroenteritis; Humans; Male; Mesenteric Lymphad

1991
Deferoxamine-induced bone dysplasia in patients with thalassemia major.
    AJR. American journal of roentgenology, 1991, Volume: 156, Issue:3

    Topics: Adolescent; Age Factors; Blood Transfusion; Bone Diseases, Developmental; Child; Deferoxamine; Femal

1991
Pseudo deep-vein thrombosis following desferrioxamine infusion: a previously unreported adverse reaction?
    Lancet (London, England), 1990, Sep-29, Volume: 336, Issue:8718

    Topics: Deferoxamine; Humans; Infusion Pumps; Male; Thalassemia; Thrombophlebitis

1990
Pulmonary syndrome and intravenous high-dose desferrioxamine.
    Lancet (London, England), 1990, Dec-15, Volume: 336, Issue:8729

    Topics: Adolescent; Child; Deferoxamine; Humans; Infusions, Intravenous; Pulmonary Fibrosis; Thalassemia

1990
Prolonged survival in patients with beta-thalassemia major treated with deferoxamine.
    The Journal of pediatrics, 1991, Volume: 118, Issue:4 Pt 1

    Topics: Adolescent; Adult; Blood Transfusion; Body Burden; Chelation Therapy; Child; Child, Preschool; Combi

1991
Hearing impairment during deferoxamine therapy for thalassemia major.
    The Journal of pediatrics, 1991, Volume: 118, Issue:5

    Topics: Adolescent; Child; Child, Preschool; Deferoxamine; Hearing Loss, Sensorineural; Humans; Thalassemia

1991
[The value of nuclear magnetic resonance in the study of iron overload in thalassemia patients].
    Annales de pediatrie, 1991, Volume: 38, Issue:3

    Topics: Adolescent; Adult; Alanine Transaminase; Cardiomyopathies; Child; Deferoxamine; Ferritins; Hemosider

1991
Immunologic evaluation of children with homozygous beta-thalassemia treated with desferrioxamine.
    Acta haematologica, 1990, Volume: 83, Issue:2

    Topics: Adolescent; Antibody Formation; Blood Bactericidal Activity; Cell Adhesion; Chemotaxis, Leukocyte; C

1990
High incidence of cardiomyopathy in beta-thalassaemia patients receiving regular transfusion and iron chelation: reversal by intensified chelation.
    Acta haematologica, 1990, Volume: 84, Issue:3

    Topics: Adolescent; Adult; Blood Transfusion; Chelation Therapy; Child; Combined Modality Therapy; Deferoxam

1990
Hypogonadism in beta-thalassemic adolescents: a characteristic pituitary-gonadal impairment. The ineffectiveness of long-term iron chelation therapy.
    Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 1990, Volume: 4, Issue:3

    Topics: Adolescent; Chelation Therapy; Child; Deferoxamine; Dose-Response Relationship, Drug; Estradiol; Fem

1990
[Yersinia infection and hemoglobin disorder. Apropos of 4 cases].
    Pediatrie, 1990, Volume: 45, Issue:6

    Topics: Anemia, Sickle Cell; Child; Deferoxamine; Female; Humans; Iron; Male; Thalassemia; Yersinia enteroco

1990
[Intravenous administration of deferoxamine in over-night hospitalization: efficacy and good psychological tolerance in thalassemic children].
    Pediatrie, 1990, Volume: 45, Issue:9

    Topics: Adolescent; Child; Child, Hospitalized; Deferoxamine; Follow-Up Studies; Humans; Infusion Pumps, Imp

1990
Treatment of Cooley's anemia: deferoxamine provocation test.
    Blood, 1990, Nov-01, Volume: 76, Issue:9

    Topics: Deferoxamine; Humans; Iron Chelating Agents; Spectrophotometry, Atomic; Thalassemia

1990
Acute changes in renal function associated with deferoxamine therapy.
    American journal of diseases of children (1960), 1990, Volume: 144, Issue:10

    Topics: Deferoxamine; Humans; Kidney Diseases; Thalassemia

1990
Current treatment of Cooley's anemia. Intravenous chelation therapy.
    Annals of the New York Academy of Sciences, 1990, Volume: 612

    Topics: Adult; Anemia, Sickle Cell; Deferoxamine; Female; Ferritins; Humans; Infusions, Intravenous; Thalass

1990
Chelation therapy and cardiac status in older patients with thalassemia major.
    The American journal of pediatric hematology/oncology, 1990,Spring, Volume: 12, Issue:1

    Topics: Adolescent; Adult; Chelation Therapy; Child; Deferoxamine; Drug Administration Schedule; Electrocard

1990
Comparison of deferoxamine pharmacokinetics between asymptomatic thalassemic children and those exhibiting severe neurotoxicity.
    Clinical pharmacology and therapeutics, 1990, Volume: 47, Issue:4

    Topics: Adolescent; Adult; Child; Child, Preschool; Chromatography, High Pressure Liquid; Deferoxamine; Dose

1990
Pulmonary syndrome in patients with thalassemia major receiving intravenous deferoxamine infusions.
    American journal of diseases of children (1960), 1990, Volume: 144, Issue:5

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Drug Hypersensitivity; Female; Humans; Imm

1990
Rapid removal of excessive iron in thalassemia by high-dose intravenous chelation therapy.
    The Journal of pediatrics, 1990, Volume: 116, Issue:1

    Topics: Adolescent; Adult; Chelation Therapy; Deferoxamine; Ferritins; Humans; Thalassemia

1990
Ocular findings in beta-thalassemia.
    Metabolic, pediatric, and systemic ophthalmology (New York, N.Y. : 1985), 1990, Volume: 13, Issue:1

    Topics: Adolescent; Adult; Blood Transfusion; Cataract; Child; Deferoxamine; Eye Diseases; Female; Humans; M

1990
Vision and hearing during deferoxamine therapy.
    The Journal of pediatrics, 1990, Volume: 117, Issue:2 Pt 1

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Chelation Therapy; Child; Deferoxamine; Ferritins; Hearing L

1990
Effect of age at the start of iron chelation therapy on gonadal function in beta-thalassemia major.
    The New England journal of medicine, 1990, Sep-13, Volume: 323, Issue:11

    Topics: Adolescent; Age Factors; Body Height; Child; Deferoxamine; Female; Ferritins; Growth Hormone; Humans

1990
Desferrioxamine improves neutrophil phagocytosis in thalassemia major.
    American journal of hematology, 1990, Volume: 35, Issue:1

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Female; Humans; Male; Neutrophils; Phagocy

1990
Acute changes in renal function associated with deferoxamine therapy.
    American journal of diseases of children (1960), 1989, Volume: 143, Issue:9

    Topics: Adolescent; Adult; Animals; Blood Urea Nitrogen; Child, Preschool; Creatinine; Deferoxamine; Dogs; F

1989
Desferrioxamine ototoxicity: evaluation of risk factors in thalassaemic patients and guidelines for safe dosage.
    British journal of haematology, 1989, Volume: 73, Issue:3

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Drug Evaluation; Female; Ferritins; Hearin

1989
Sustained normalization of cardiac function by chelation therapy in thalassaemia major.
    Clinical and laboratory haematology, 1989, Volume: 11, Issue:4

    Topics: Adolescent; Adult; Australia; Blood Transfusion; Chelation Therapy; Child; Combined Modality Therapy

1989
Use of the ferritin/alanine aspartate transaminase ratio as an iron overload marker independent of liver cell damage.
    European journal of haematology, 1989, Volume: 43, Issue:5

    Topics: Alanine Transaminase; Aspartate Aminotransferases; Biomarkers; Blood Transfusion; Combined Modality

1989
Mineral balance (iron, aluminum, copper, zinc) after high-dose intravenous Desferal in a child with hemoglobin Hammersmith and Turner's syndrome.
    The American journal of pediatric hematology/oncology, 1989,Winter, Volume: 11, Issue:4

    Topics: Child; Deferoxamine; Feces; Female; Hemoglobins, Abnormal; Humans; Minerals; Thalassemia; Turner Syn

1989
Liver iron stores before and after bone marrow transplantation for thalassemia.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Bone Marrow Transplantation; Busulfan; Child; Cyclophosphamide; Deferoxamine; Ferritins; Graft vs Ho

1989
Iron excretion in thalassemia children treated with deferoxamin methansulfonat: intravenous drip compared to the subcutaneous routes.
    Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1989, Volume: 72 Suppl 1

    Topics: Adolescent; Child; Deferoxamine; Humans; Infusion Pumps; Infusions, Intravenous; Iron; Male; Thalass

1989
[Treatment of post-transfusion iron overload by deferoxamine].
    Archives francaises de pediatrie, 1989, Volume: 46, Issue:2

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Child; Deferoxamine; Ferritins; Hemochromatosis; Humans; Tha

1989
Rapid removal of excessive iron with daily, high-dose intravenous chelation therapy.
    The Journal of pediatrics, 1989, Volume: 115, Issue:1

    Topics: Adolescent; Adult; Anemia, Aplastic; Anemia, Sickle Cell; Catheterization, Central Venous; Deferoxam

1989
A high-performance liquid chromatographic method for the measurement of deferoxamine in body fluids.
    Therapeutic drug monitoring, 1989, Volume: 11, Issue:4

    Topics: Adolescent; Animals; Chromatography, High Pressure Liquid; Ciprofloxacin; Deferoxamine; Dogs; Humans

1989
Studies of variations of subcutaneously infused desferrioxamine and iron movements in thalassaemia children.
    European journal of pediatrics, 1989, Volume: 148, Issue:6

    Topics: Adolescent; Child; Deferoxamine; Female; Ferric Compounds; Hemochromatosis; Humans; Infusions, Paren

1989
Hepatic iron stores in thalassemia: non-invasive magnetic measurements.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Blood Transfusion; Deferoxamine; Ferritins; Humans; Iron Chelating Agents; Liver; Magnetics; Thalass

1989
High-dose intravenous chelation therapy with deferoxamine.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Blood Transfusion; Deferoxamine; Ferritins; Humans; Infusion

1989
Medical management of beta-thalassemia.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Erythrocyte Transfusion; Ferritins; Heart

1989
Quality of life and life expectancy in thalassemic patients with complications.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Diabetes Mellitus, Type 1; Heart Diseases

1989
Compliance with therapy in Cooley's anaemia.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Blood Transfusion; Deferoxamine; Humans; Iron; Iron Chelating Agents; Patient Compliance; Penicillin

1989
Cardiac complications in homozygous beta-thalassemia.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Female; Heart Diseases; Homozygote; Human

1989
Endocrine complications in thalassaemia major.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Blood Transfusion; Deferoxamine; Diabetes Mellitus, Type 1; Female; Humans; Hypog

1989
Concomitant primary hemochromatosis and beta-thalassemia trait: iron depletion by erythrocytapheresis and desferrioxamine.
    The American journal of gastroenterology, 1989, Volume: 84, Issue:2

    Topics: Adult; Blood Component Removal; Deferoxamine; Erythrocytes; Female; Ferritins; Hemochromatosis; Huma

1989
Reversal of desferrioxamine induced auditory neurotoxicity during treatment with Ca-DTPA.
    Archives of disease in childhood, 1989, Volume: 64, Issue:1

    Topics: Adolescent; Adult; Audiometry; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Female; Fer

1989
Long-term effect of splenectomy on transfusion requirements in thalassemia major.
    American journal of hematology, 1989, Volume: 30, Issue:4

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Ferritins; Humans; Iron

1989
Infection with Yersinia enterocolitica in patients with iron overload.
    British medical journal (Clinical research ed.), 1986, Jan-11, Volume: 292, Issue:6513

    Topics: Adult; Anemia, Sideroblastic; Blood Transfusion; Deferoxamine; Female; Hemosiderosis; Humans; Male;

1986
Yersinia and iron overload.
    British medical journal (Clinical research ed.), 1986, Feb-08, Volume: 292, Issue:6517

    Topics: Deferoxamine; Female; Humans; Infant; Thalassemia; Yersinia enterocolitica; Yersinia Infections

1986
Non-transferrin-bound iron in long-term transfusion in children with congenital anemias.
    The Journal of pediatrics, 1986, Volume: 108, Issue:4

    Topics: Adolescent; Adult; Anemia, Hemolytic, Congenital; Anemia, Sickle Cell; Anemia, Sideroblastic; Bindin

1986
Reappraisal of high-dose desferrioxamine therapy.
    Acta haematologica, 1986, Volume: 76, Issue:1

    Topics: Deferoxamine; Hemosiderosis; Humans; Thalassemia; Transfusion Reaction

1986
Iron state and hepatic disease in patients with thalassaemia major, treated with long term subcutaneous desferrioxamine.
    Journal of clinical pathology, 1987, Volume: 40, Issue:11

    Topics: Adolescent; Adult; Child; Deferoxamine; Female; Ferritins; Hepatitis; Hepatitis B Core Antigens; Hep

1987
Coagulation contact phase factors and inhibitors in beta-thalassemia major children.
    Pediatric hematology and oncology, 1987, Volume: 4, Issue:3

    Topics: Adolescent; Blood Coagulation Disorders; Child; Combined Modality Therapy; Deferoxamine; Humans; Pla

1987
Deferoxamine-induced growth retardation in patients with thalassemia major.
    The Journal of pediatrics, 1988, Volume: 113, Issue:4

    Topics: Body Height; Bone and Bones; Deferoxamine; Dose-Response Relationship, Drug; Female; Growth Disorder

1988
Hearing loss and desferrioxamine in homozygous beta-thalassemia.
    Audiology : official organ of the International Society of Audiology, 1988, Volume: 27, Issue:4

    Topics: Adolescent; Audiometry; Child; Deferoxamine; Female; Hearing Loss, Conductive; Hearing Loss, Sensori

1988
Desferrioxamine and ascorbic acid supplement in E-B thalassaemia.
    The Journal of the Association of Physicians of India, 1988, Volume: 36, Issue:7

    Topics: Ascorbic Acid; Child; Child, Preschool; Deferoxamine; Humans; Thalassemia

1988
Yersinia enterocolitica septicaemia.
    Intensive care medicine, 1988, Volume: 14, Issue:5

    Topics: Adult; Deferoxamine; Hemosiderosis; Humans; Sepsis; Thalassemia; Yersinia enterocolitica; Yersinia I

1988
Maintenance treatment with desferrioxamine via subcutaneous injections in a patient with HbE thalassaemia.
    The Netherlands journal of medicine, 1988, Volume: 33, Issue:3-4

    Topics: Adult; Deferoxamine; Hemoglobin E; Hemoglobins, Abnormal; Humans; Injections, Subcutaneous; Male; Th

1988
Can deferoxamine be considered an ototoxic drug?
    Scandinavian audiology. Supplementum, 1988, Volume: 30

    Topics: Adolescent; Adult; Child; Deferoxamine; Hearing Loss, Sensorineural; Humans; Thalassemia

1988
Pneumocystis carinii pneumonia as a complication of desferrioxamine therapy.
    British journal of haematology, 1988, Volume: 70, Issue:3

    Topics: Adult; Deferoxamine; Humans; Male; Pneumonia, Pneumocystis; Thalassemia

1988
A prospective evaluation of iron chelation therapy in children with severe beta-thalassemia. A six-year study.
    American journal of diseases of children (1960), 1988, Volume: 142, Issue:3

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Growth; Heart Diseases; Humans; Iron; Live

1988
Electroretinographic and visual-evoked potential abnormalities in patients with beta-thalassemia major.
    Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 1988, Volume: 196, Issue:1

    Topics: Adolescent; Adult; Child; Deferoxamine; Electroretinography; Evoked Potentials, Visual; Eye; Humans;

1988
Depletion of trace elements and acute ocular toxicity induced by desferrioxamine in patients with thalassaemia.
    Archives of disease in childhood, 1988, Volume: 63, Issue:3

    Topics: Adolescent; Child; Copper; Deferoxamine; Electroretinography; Humans; Infusions, Intravenous; Retina

1988
High-dose desferrioxamine as a cause of growth failure in thalassemic patients.
    European journal of haematology, 1988, Volume: 40, Issue:4

    Topics: Child; Child, Preschool; Deferoxamine; Female; Ferritins; Growth Disorders; Humans; Male; Thalassemi

1988
Hearing loss attributed to desferrioxamine in patients with beta-thalassaemia major.
    The Medical journal of Australia, 1988, Jun-20, Volume: 148, Issue:12

    Topics: Deferoxamine; Hearing Loss, Sensorineural; Humans; Thalassemia

1988
Subcutaneous diethylene triamine pentaacetic acid: comparison with desferrioxamine in thalassemic patients with iron overload.
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Adult; Child; Deferoxamine; Female; Humans; Infusions, Parenteral; Iron; Male; Pentetic Acid; Thalas

1988
Iron status in thalassemia major patients after long-term subcutaneous desferrioxamine.
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Adolescent; Adult; Child; Deferoxamine; Female; Humans; Infusions, Parenteral; Iron; Male; Splenecto

1988
Normal serum ferritin levels following prolonged desferrioxamine therapy: Melbourne experience.
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Ferritins; Humans; Thalassemia; Time Facto

1988
Rubber band technique for slow subcutaneous infusion of desferrioxamine (Desferal).
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Adolescent; Child; Child, Preschool; Deferoxamine; Female; Humans; Infusions, Parenteral; Iron; Male

1988
Oral ascorbic acid and iron excretion in thalassemic children treated with desferrioxamine-methansulfonate (Desferal).
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Administration, Oral; Adolescent; Ascorbic Acid; Child; Child, Preschool; Deferoxamine; Drug Therapy

1988
Effects of deferoxamine on renal function in thalassemia.
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Adolescent; Adult; Child; Deferoxamine; Female; Humans; Kidney; Kidney Function Tests; Male; Thalass

1988
Iron balance and the management of iron overload in beta-thalassemia intermedia.
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Administration, Cutaneous; Administration, Oral; Adolescent; Adult; Deferoxamine; Female; Humans; Ir

1988
Iron chelation in thalassemia.
    Birth defects original article series, 1988, Volume: 23, Issue:5B

    Topics: Ascorbic Acid Deficiency; Deferoxamine; Dose-Response Relationship, Drug; Humans; Iron; Thalassemia

1988
Modulation of the defective natural killer activity seen in thalassaemia major with desferrioxamine and alpha-interferon.
    Clinical and experimental immunology, 1987, Volume: 70, Issue:2

    Topics: Cytotoxicity, Immunologic; Deferoxamine; Fibroblasts; Herpes Simplex; Humans; Interferon Type I; Kil

1987
[Yersinia septicemia in children with thalassaemia major].
    Changgeng yi xue za zhi, 1987, Jun-20, Volume: 10, Issue:2

    Topics: Child; Child, Preschool; Deferoxamine; Female; Hemosiderosis; Humans; Male; Risk Factors; Sepsis; Th

1987
Visual and auditory neurotoxicity in patients receiving subcutaneous deferoxamine infusions.
    The New England journal of medicine, 1986, Apr-03, Volume: 314, Issue:14

    Topics: Adolescent; Adult; Age Factors; Anemia, Aplastic; Audiometry; Child; Child, Preschool; Color Vision

1986
[Continuous subcutaneous deferoxamine infusions in thalassemia major. Improvement in glucose tolerance].
    Deutsche medizinische Wochenschrift (1946), 1986, May-02, Volume: 111, Issue:18

    Topics: Adolescent; Adult; alpha-Amylases; Blood Glucose; Child; Child, Preschool; Deferoxamine; Diabetes Co

1986
The development of diabetes mellitus and chronic liver disease in long term chelated beta thalassaemic patients.
    Postgraduate medical journal, 1986, Volume: 62, Issue:731

    Topics: Adolescent; Adult; Blood Glucose; Child; Chronic Disease; Deferoxamine; Diabetes Mellitus; Female; F

1986
[Hypertransfusion, chelating and immunocorrective therapy in beta-thalassemia major].
    Pediatriia, 1987, Issue:2

    Topics: Blood Transfusion; Chelating Agents; Child; Child, Preschool; Combined Modality Therapy; Deferoxamin

1987
Yersinia hepatic abscesses and iron overload.
    JAMA, 1987, Jun-19, Volume: 257, Issue:23

    Topics: Child; Child, Preschool; Deferoxamine; Female; Humans; Iron; Male; Thalassemia; Yersinia enterocolit

1987
Leukocyte alkaline phosphatase (LAP). A useful marker of zinc status in beta-thalassemic patients.
    The American journal of pediatric hematology/oncology, 1987,Summer, Volume: 9, Issue:2

    Topics: Adolescent; Alkaline Phosphatase; Child; Child, Preschool; Deferoxamine; Humans; Leukocytes; Neutrop

1987
Hearing loss attributed to desferrioxamine in patients with beta-thalassaemia major.
    The Medical journal of Australia, 1987, Aug-17, Volume: 147, Issue:4

    Topics: Adolescent; Adult; Child; Deferoxamine; Drug Administration Schedule; Hearing Loss, Sensorineural; H

1987
Comparison between serum ferritin and computed tomographic densities of liver, spleen, kidney and pancreas in beta-thalassaemia major.
    Scandinavian journal of clinical and laboratory investigation, 1987, Volume: 47, Issue:7

    Topics: Blood Transfusion; Child; Child, Preschool; Deferoxamine; Ferritins; Humans; Liver; Liver Cirrhosis;

1987
[Effect of desferal therapy on indices of iron metabolism in patients with intermediate forms of beta-thalassemia].
    Gematologiia i transfuziologiia, 1987, Volume: 32, Issue:9

    Topics: Adolescent; Adult; Blood Transfusion; Deferoxamine; Female; Globins; Homozygote; Humans; Iron; Iron

1987
Yersinia sepsis in patients with iron overload treated with deferoxamine.
    The New England journal of medicine, 1986, Jun-19, Volume: 314, Issue:25

    Topics: Adult; Deferoxamine; Female; Humans; Iron; Thalassemia; Yersinia enterocolitica; Yersinia Infections

1986
Iron chelation using subcutaneous infusions of diethylene triamine penta-acetic acid (DTPA).
    Scandinavian journal of haematology, 1986, Volume: 36, Issue:5

    Topics: Administration, Oral; Adult; Ascorbic Acid; Child; Deferoxamine; Dose-Response Relationship, Drug; D

1986
Effect of desferrioxamine on salivary iron in thalassemic children.
    Israel journal of medical sciences, 1986, Volume: 22, Issue:6

    Topics: Child; Deferoxamine; Humans; Iron; Saliva; Thalassemia

1986
Deferoxamine improves left ventricular function in beta-thalassemia.
    Archives of internal medicine, 1986, Volume: 146, Issue:12

    Topics: Adolescent; Adult; Child; Deferoxamine; Echocardiography; Female; Ferritins; Heart; Heart Ventricles

1986
Nontransferrin-bound serum iron in thalassemia and sickle cell patients.
    The International journal of biochemistry, 1986, Volume: 18, Issue:10

    Topics: Adult; Anemia, Sickle Cell; Chromatography, Ion Exchange; Deferoxamine; Electrophoresis, Polyacrylam

1986
Quantification of desferrioxamine in blood plasma by inductively coupled plasma atomic emission spectrometry.
    Clinical chemistry, 1987, Volume: 33, Issue:1

    Topics: Colorimetry; Deferoxamine; Humans; Indicators and Reagents; Kidney Failure, Chronic; Quality Control

1987
[Thalassemia major: chelating therapy with deferoxamine].
    Medicina, 1985, Volume: 45, Issue:3

    Topics: Adolescent; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Female; Ferritins; Humans; Inj

1985
Current therapy and new approaches to the treatment of thalassemia major.
    Annals of the New York Academy of Sciences, 1985, Volume: 445

    Topics: Adolescent; Blood Transfusion; Child; Deferoxamine; Erythrocytes; Humans; Iron; Male; Pyruvate Kinas

1985
Treatment of iron overload in Cooley's anemia.
    Annals of the New York Academy of Sciences, 1985, Volume: 445

    Topics: Adolescent; Adult; Blood Transfusion; Chelating Agents; Child; Child, Preschool; Deferoxamine; Eryth

1985
The effect of subcutaneous deferoxamine on the cardiac profile of thalassemia major: a five-year study.
    Annals of the New York Academy of Sciences, 1985, Volume: 445

    Topics: Adolescent; Adult; Arrhythmias, Cardiac; Child; Child, Preschool; Deferoxamine; Echocardiography; El

1985
Combined subcutaneous and high-dose intravenous deferoxamine therapy of thalassemia.
    Annals of the New York Academy of Sciences, 1985, Volume: 445

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Echocardiography; Ferri

1985
Improved oxygen delivery to tissues and iron chelator transport through the use of lysed and resealed red blood cells: a new perspective on Cooley's anemia therapy.
    Annals of the New York Academy of Sciences, 1985, Volume: 445

    Topics: Animals; Blood Transfusion; Chelating Agents; Deferoxamine; Erythrocyte Aging; Erythrocyte Transfusi

1985
Defective vitamin D metabolism in thalassemia major.
    Annals of the New York Academy of Sciences, 1985, Volume: 445

    Topics: Adolescent; Adult; Calcitriol; Calcium; Chelating Agents; Child; Child, Preschool; Deferoxamine; Erg

1985
The chronically transfused patient: advances in treatment.
    Hospital practice (Office ed.), 1985, Jul-15, Volume: 20, Issue:7

    Topics: Acquired Immunodeficiency Syndrome; Adult; Blood Grouping and Crossmatching; Blood Transfusion; Chil

1985
[Longitudinal growth of patients with homozygote beta-thalassemia during continuous subcutaneous infusion of deferoxamine].
    Deutsche medizinische Wochenschrift (1946), 1986, Jan-31, Volume: 111, Issue:5

    Topics: Age Determination by Skeleton; Body Height; Child; Child, Preschool; Deferoxamine; Female; Greece; H

1986
High-dose desferoxamine and Diamond-Blackfan anemia.
    Annals of internal medicine, 1986, Volume: 104, Issue:4

    Topics: Adolescent; Anemia; Deferoxamine; Heart Failure; Humans; Infusions, Parenteral; Thalassemia; Transfu

1986
Growth and sexual maturation in thalassemia major.
    The Journal of pediatrics, 1985, Volume: 106, Issue:1

    Topics: Adolescent; Adult; Age Determination by Skeleton; Amenorrhea; Blood Transfusion; Body Height; Child;

1985
Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major.
    The New England journal of medicine, 1985, Jun-20, Volume: 312, Issue:25

    Topics: Adolescent; Arrhythmias, Cardiac; Aspartate Aminotransferases; Cardiomyopathies; Child; Deferoxamine

1985
Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major.
    The New England journal of medicine, 1985, Jun-20, Volume: 312, Issue:25

    Topics: Adolescent; Arrhythmias, Cardiac; Aspartate Aminotransferases; Cardiomyopathies; Child; Deferoxamine

1985
Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major.
    The New England journal of medicine, 1985, Jun-20, Volume: 312, Issue:25

    Topics: Adolescent; Arrhythmias, Cardiac; Aspartate Aminotransferases; Cardiomyopathies; Child; Deferoxamine

1985
Prevention of cardiac disease by subcutaneous deferoxamine in patients with thalassemia major.
    The New England journal of medicine, 1985, Jun-20, Volume: 312, Issue:25

    Topics: Adolescent; Arrhythmias, Cardiac; Aspartate Aminotransferases; Cardiomyopathies; Child; Deferoxamine

1985
Ocular and auditory toxicity of long-term, high-dose subcutaneous deferoxamine therapy.
    Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 1985, Volume: 20, Issue:4

    Topics: Child, Preschool; Deferoxamine; Ear; Eye; Female; Hearing Loss, Sensorineural; Humans; Injections, S

1985
[Continuous subcutaneous deferoxamine treatment in thalassemia major. Decrease of hemosiderosis and improvement of liver function].
    Deutsche medizinische Wochenschrift (1946), 1985, Nov-29, Volume: 110, Issue:48

    Topics: Adolescent; Adult; Child; Child, Preschool; Deferoxamine; Hemosiderosis; Humans; Injections, Subcuta

1985
[Effect of two years of deferoxamine therapy on iron balance, ferritin, liver and heart in patients with thalassemia major].
    Helvetica paediatrica acta, 1985, Volume: 40, Issue:4

    Topics: Adolescent; Child; Child, Preschool; Deferoxamine; Ferritins; Heart; Humans; Iron; Liver; Patient Co

1985
[Severe cardiomyopathy in a woman with intermediate beta-thalassemia. Regression of cardiac failure with desferrioxamine].
    Giornale italiano di cardiologia, 1985, Volume: 15, Issue:9

    Topics: Adult; Deferoxamine; Echocardiography; Electrocardiography; Female; Heart Failure; Humans; Thalassem

1985
[Current treatment of Cooley's disease].
    Annales de pediatrie, 1985, Volume: 32, Issue:9

    Topics: Blood Grouping and Crossmatching; Blood Transfusion; Child; Deferoxamine; Erythrocyte Transfusion; H

1985
[Desferal test in the diagnosis of hemosiderosis in patents with hemoglobinopathies].
    Laboratornoe delo, 1971, Volume: 11

    Topics: Adolescent; Adult; Aged; Anemia, Sickle Cell; Child; Child, Preschool; Deferoxamine; Female; Hemoglo

1971
Clinical experience with intensive transfusion therapy in Cooley's anemia.
    Annals of the New York Academy of Sciences, 1969, Nov-20, Volume: 165, Issue:1

    Topics: 17-Ketosteroids; Blood Transfusion; Bone Development; Calcium; Child; Deferoxamine; Electrocardiogra

1969
[Research on the effect of desferrioxamine B in patients with Cooley's disease].
    Il Policlinico. Sezione pratica, 1967, Dec-11, Volume: 74, Issue:50

    Topics: Adolescent; Adult; Cardiomegaly; Child; Child, Preschool; Deferoxamine; Female; Hepatomegaly; Humans

1967
Long-term administration of desferrioxamine in thalassaemia major.
    Archives of disease in childhood, 1974, Volume: 49, Issue:8

    Topics: Adolescent; Adult; Aspartate Aminotransferases; Bilirubin; Blood Protein Electrophoresis; Blood Tran

1974
Ascorbic acid enhancement of desferrioxamine-induced urinary iron excretion in thalassemia major.
    Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0

    Topics: Administration, Oral; Adolescent; Adult; Age Factors; Ascorbic Acid; Child; Child, Preschool; Defero

1974
Combined long-term treatment of hemosiderosis with desferioxamine and DTPA in homozygous beta-thalassemia.
    Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Drug Therapy, Combination; Erythrocytes;

1974
Long-term desferrioxamine therapy in thalassemia.
    Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0

    Topics: Adolescent; Ascorbic Acid; Child; Child, Preschool; Cyprus; Deferoxamine; Drug Synergism; Humans; Ir

1974
Urinary iron excretion in thalassaemia after desferrioxamine administration.
    Archives of disease in childhood, 1974, Volume: 49, Issue:3

    Topics: Adolescent; Adult; Blood Transfusion; Child; Child, Preschool; Deferoxamine; Female; Hemoglobins; Hu

1974
Editorial: Thalassemia major: a problem of iron overload.
    Annals of internal medicine, 1974, Volume: 81, Issue:2

    Topics: Ascorbic Acid; Chelating Agents; Child; Child, Preschool; Deferoxamine; Humans; Intestinal Absorptio

1974
[Hemochromatosis].
    Munchener medizinische Wochenschrift (1950), 1972, Feb-04, Volume: 114, Issue:5

    Topics: Adult; Anemia, Macrocytic; Bloodletting; Deferoxamine; Diagnosis, Differential; Diet Therapy; Female

1972
The effective use of oxymetholone in the therapy of thalassaemia with anaemia.
    The Medical journal of Australia, 1972, Sep-23, Volume: 2, Issue:13

    Topics: Adult; Child; Deferoxamine; Hemosiderosis; Humans; Oxymetholone; Thalassemia

1972
[Treatment of Cooley's anemia].
    Archivos argentinos de pediatria, 1971, Volume: 69, Issue:6

    Topics: Blood Transfusion; Deferoxamine; Glucocorticoids; Humans; Splenectomy; Thalassemia

1971
Some clinical features of Cooley's anemia patients as related to transfusion schedules.
    Annals of the New York Academy of Sciences, 1969, Nov-20, Volume: 165, Issue:1

    Topics: Blood Transfusion; Deferoxamine; Fetal Hemoglobin; Growth Disorders; Hematopoiesis; Humans; Iron; Li

1969
Management of thalassemia: a comparative program.
    Annals of the New York Academy of Sciences, 1969, Nov-20, Volume: 165, Issue:1

    Topics: Adolescent; Asian People; Blood Transfusion; Body Height; Body Weight; Child; Child, Preschool; Defe

1969
Prevention of bone malformations and cardiomegaly in Cooley's anemia by early hypertransfusion regimen.
    Annals of the New York Academy of Sciences, 1969, Nov-20, Volume: 165, Issue:1

    Topics: Blood Transfusion; Bone Diseases, Developmental; Cardiomyopathies; Child; Child, Preschool; Deferoxa

1969
A comparison of desferrioxamine-induced sideruria and measurement of labile iron store as indices of body iron status.
    Journal of medicine, 1971, Volume: 2, Issue:6

    Topics: Adult; Anemia, Hypochromic; Anemia, Macrocytic; Autoanalysis; Body Composition; Chelating Agents; De

1971
[Therapy of primary siderochromatosis and siderosis: experimental and clinical study].
    Minerva medica, 1969, Dec-03, Volume: 60, Issue:97

    Topics: Bloodletting; Deferoxamine; Hemochromatosis; Humans; Intestinal Absorption; Iron; Porphyrias; Primar

1969
[Inveterate leg ulcer in a constitutional hemolytic syndrome with dermosiderosis. Cure by desfrrioxamine].
    Bulletin de la Societe francaise de dermatologie et de syphiligraphie, 1967, Volume: 74, Issue:4

    Topics: Adult; Deferoxamine; Humans; Leg Ulcer; Male; Siderosis; Skin Diseases; Thalassemia

1967
[Importance of treatment with deferoxamine in children with Cooley's disease].
    Minerva pediatrica, 1967, Dec-15, Volume: 19, Issue:50

    Topics: Child; Child, Preschool; Deferoxamine; Female; Humans; Male; Thalassemia

1967
[Current status of treatments with desferrioxamine B in post-transfusion hypersiderosis in children].
    Marseille medical, 1967, Volume: 104, Issue:4

    Topics: Adolescent; Anemia, Aplastic; Anemia, Hemolytic; Child; Child, Preschool; Deferoxamine; Female; Hemo

1967
Desferrioxamine in thalassaemia.
    Archives of disease in childhood, 1968, Volume: 43, Issue:229

    Topics: Adolescent; Bone Marrow; Cataract; Child; Child, Preschool; Deferoxamine; Female; Hemoglobinometry;

1968
[Clinical and metabolic research on treatment with desferrioxamine B in various hemosiderotic erythrocyte diseases].
    La Clinica terapeutica, 1965, Jul-15, Volume: 34, Issue:1

    Topics: Adolescent; Adult; Aged; Anemia; Child; Child, Preschool; Deferoxamine; Female; Hemosiderosis; Human

1965
[Remarks on the treatment of thalassemia major].
    Kinderarztliche Praxis, 1965, Volume: 33, Issue:8

    Topics: Child; Child, Preschool; Deferoxamine; Humans; Splenectomy; Thalassemia

1965
[Use of desferrioxamine B in the treatment of post-transfusion hypersiderosis].
    Marseille medical, 1965, Volume: 102, Issue:7

    Topics: Adolescent; Anemia, Hemolytic; Child; Child, Preschool; Deferoxamine; Female; Humans; Male; Siderosi

1965
Deferoxamine and diethylenetriaminepentaacetic acid (DTPA) in thalassemia.
    The Journal of pediatrics, 1966, Volume: 69, Issue:4

    Topics: Child; Deferoxamine; Female; Humans; Infant; Iron; Male; Pentetic Acid; Thalassemia

1966
[Effects of desferrioxamine on iron elimination in children after multiple transfusions].
    Minerva pediatrica, 1966, Feb-04, Volume: 18, Issue:3

    Topics: Blood Transfusion; Child; Deferoxamine; Hemosiderosis; Humans; Iron; Thalassemia

1966
[Thoughts apropos of 2 cases of major thalassemia and its treatment by desferrioxamine B].
    Pediatrie, 1966, Volume: 21, Issue:6

    Topics: Child; Deferoxamine; Female; Humans; Infant; Male; Splenectomy; Thalassemia

1966
[Desferrioxamine-B in the diagnosis of hemosiderotic states and in the therapy of thalassemia. Apropos of 2 cases].
    Minerva pediatrica, 1966, Oct-27, Volume: 18, Issue:32

    Topics: Child; Child, Preschool; Deferoxamine; Hemosiderosis; Humans; Iron; Male; Thalassemia

1966
The treatment of hemosiderosis in thalassaemia major with desferrioxamine-B.
    Helvetica paediatrica acta, 1966, Volume: 21, Issue:4

    Topics: Adolescent; Anemia, Sickle Cell; Biopsy; Child; Deferoxamine; Female; Hemochromatosis; Hemosiderosis

1966