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deferoxamine and Cardiac Failure

deferoxamine has been researched along with Cardiac Failure in 47 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
"To evaluate the effects of the iron chelator deferoxamine on the functional and structural manifestations of iron-induced cardiac dysfunction, we measured cardiac power, left ventricular systolic, and diastolic function as (dP/dt)max and (dP/dt)min, respectively, and left ventricular and septal wall thickness in isolated heart preparations derived from the Mongolian gerbil model of iron overload."7.72Deferoxamine prevents cardiac hypertrophy and failure in the gerbil model of iron-induced cardiomyopathy. ( Brittenham, GM; Brown, AM; Dong, WQ; Kuryshev, YA; Levy, MN; Obejero-Paz, CA; Yang, T, 2003)
"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)
"We enrolled nine patients with thalassemia major complicated by some degree of myocardial dysfunction."5.33Regression of myocardial dysfunction after switching from desferrioxamine to deferiprone therapy in beta-thalassemia major patients. ( Chang, JS; Huang, YC; Peng, CT; Wu, KH, 2006)
"Deferiprone (L1) was found to have greater efficacy at depleting myocardial iron than desferrioxamine (DFX)."5.32Combined therapy with deferiprone and desferrioxamine successfully regresses severe heart failure in patients with beta-thalassemia major. ( Chang, JS; Peng, CT; Tsai, CH; Wu, KH, 2004)
" In thalassemia major patients, combined therapy with desferrioxamine and deferiprone has maximized tissue iron removal and may reduce the overall occurrence of hemosiderotic heart failure."3.73Transfusional hemosiderosis and combined chelation therapy in sickle thalassemia. ( Aessopos, A; Andriopoulos, P; Deftereos, S; Farmakis, D; Moyssakis, I; Polonifi, K; Tsironi, M, 2005)
"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)
"To evaluate the effects of the iron chelator deferoxamine on the functional and structural manifestations of iron-induced cardiac dysfunction, we measured cardiac power, left ventricular systolic, and diastolic function as (dP/dt)max and (dP/dt)min, respectively, and left ventricular and septal wall thickness in isolated heart preparations derived from the Mongolian gerbil model of iron overload."3.72Deferoxamine prevents cardiac hypertrophy and failure in the gerbil model of iron-induced cardiomyopathy. ( Brittenham, GM; Brown, AM; Dong, WQ; Kuryshev, YA; Levy, MN; Obejero-Paz, CA; Yang, T, 2003)
"Strict lifelong adherence to the standard transfusion and deferoxamine therapy reduces considerably the occurrence of heart failure, LV dysfunction and pericarditis, prevents early heart failure and pulmonary hypertension, but does not eliminate completely cardiac disease in patients with thalassemia major."3.72Cardiac status in well-treated patients with thalassemia major. ( Aessopos, A; Diamanti-Kandaraki, E; Farmakis, D; Fragodimitri, C; Hatziliami, A; Joussef, J; Karabatsos, F; Karagiorga, M; Meletis, J; Mitilineou, E, 2004)
"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)
"Treatment with deferasirox significantly improves left ventricular function."2.77Cardiac iron removal and functional cardiac improvement by different iron chelation regimens in thalassemia major patients. ( Brevi, F; Cappellini, MD; Cassinerio, E; Graziadei, G; Milazzo, A; Pattoneri, P; Pedrotti, P; Roghi, A; Zanaboni, L, 2012)
"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)
"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)
"Juvenile hemochromatosis is the most severe form of iron overloading phenotype."1.48Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report. ( Cooray, SD; Hamblin, PS; Heerasing, NM; Leet, AS; McDonald, CJ; McLean, CA; McNamara, E; Roberts, SK; Selkrig, LA; Subramaniam, VN, 2018)
"In patients with thalassemia major (TM) who are non-compliant with long-term desferrioxamine (DFO) chelation, survival is limited mainly because of cardiac complications of transfusional hemosiderosis."1.33Reversal of heart failure in thalassemia major by combined chelation therapy: a case report. ( Aessopos, A; Andriopoulos, P; Deftereos, S; Farmakis, D; Meletis, J; Tsironi, M, 2005)
"We enrolled nine patients with thalassemia major complicated by some degree of myocardial dysfunction."1.33Regression of myocardial dysfunction after switching from desferrioxamine to deferiprone therapy in beta-thalassemia major patients. ( Chang, JS; Huang, YC; Peng, CT; Wu, KH, 2006)
"Deferiprone (L1) was found to have greater efficacy at depleting myocardial iron than desferrioxamine (DFX)."1.32Combined therapy with deferiprone and desferrioxamine successfully regresses severe heart failure in patients with beta-thalassemia major. ( Chang, JS; Peng, CT; Tsai, CH; Wu, KH, 2004)
"A 21-year-old woman with beta-thalassemia major (beta-TM) and GH deficiency developed end-stage heart failure, New York Heart Association (NYHA) functional class IV, within 3 months after withdrawal of recombinant human growth hormone (GH)."1.32Is growth hormone deficiency contributing to heart failure in patients with beta-thalassemia major? ( Erfurth, EM; Holmer, H; Kornhall, B; Nilsson, PG, 2004)
"Juvenile haemochromatosis is a rare inborn error of iron metabolism with clinical manifestations before 30 years of age."1.30Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage disease. ( Cox, TM; Kelly, AL; Rhodes, DA; Roland, JM; Schofield, P, 1998)
"A case of severe cardiac failure due to iron overload in a patient with beta-thalassemia major is reported."1.29Regression of cardiac insufficiency after ambulatory intravenous deferoxamine in thalassemia major. ( Balmer-Ruedin, D; Halperin, DS; Oberhansli, I; Wacker, P; Wyss, M, 1993)
"Dobutamine is a sympathomimetic drug (beta 1 agonist) that increases myocardial contractility and at high doses also systolic arterial blood pressure and heart rate."1.29Cardiac study by dobutamine stress echocardiography in thalassemic patients. ( Agostini, A; Angelucci, E; Cesaroni, P; Lucarelli, G; Mariotti, E; Sgarbi, E, 1993)
"Severe congestive cardiac failure developed in a few weeks in a 44 year old man who had undergone porto-caval anastamosis for post-hepatitis cirrhosis one year previously and then treated for anaemia by repeated blood transfusion and chronic daily oral iron therapy."1.27[Adiastole caused by a secondary cardiac hemochromatosis. Successful treatment with an iron chelating agent]. ( Azancot, I; Baudouy, P; Lombrail, P; Martin, E; Piekarski, A; Slama, R, 1983)
"Idiopathic hemochromatosis is an iron-storage disease more common in men than in women."1.26Idiopathic hemochromatosis: case report of a patient presenting with neurologic symptoms. ( Afrooz, N; Sinclair, WP, 1977)

Research

Studies (47)

TimeframeStudies, this research(%)All Research%
pre-199015 (31.91)18.7374
1990's6 (12.77)18.2507
2000's19 (40.43)29.6817
2010's5 (10.64)24.3611
2020's2 (4.26)2.80

Authors

AuthorsStudies
Chuang, TY1
Li, JP1
Weng, TF1
Wu, KH4
Chao, YH1
Johnson, AC1
Zager, RA1
Cooray, SD1
Heerasing, NM1
Selkrig, LA1
Subramaniam, VN1
Hamblin, PS1
McDonald, CJ1
McLean, CA1
McNamara, E1
Leet, AS1
Roberts, SK1
Porter, JB1
Wood, J1
Olivieri, N1
Vichinsky, EP1
Taher, A1
Neufeld, E1
Giardina, P1
Thompson, A1
Moore, B1
Evans, P1
Kim, HY1
Macklin, EA1
Trachtenberg, F1
Origa, R1
Danjou, F1
Cossa, S1
Matta, G1
Bina, P1
Dessì, C2
Defraia, E1
Foschini, ML1
Leoni, G1
Morittu, M1
Galanello, R2
Tauchenová, L1
Křížová, B1
Kubánek, M1
Fraňková, S1
Melenovský, V1
Tintěra, J1
Kautznerová, D1
Malušková, J1
Jirsa, M1
Kautzner, J1
Peng, CT3
Chang, JS3
Tsai, CH2
Lin, HS1
Omiya, S1
Hikoso, S1
Imanishi, Y1
Saito, A1
Yamaguchi, O1
Takeda, T1
Mizote, I1
Oka, T1
Taneike, M1
Nakano, Y1
Matsumura, Y1
Nishida, K1
Sawa, Y1
Hori, M1
Otsu, K1
Cassinerio, E1
Roghi, A1
Pedrotti, P1
Brevi, F1
Zanaboni, L1
Graziadei, G1
Pattoneri, P1
Milazzo, A1
Cappellini, MD3
SCOVILLE, B1
BORCHERS, HG1
SCHAUER, A1
Yang, T1
Brittenham, GM1
Dong, WQ1
Levy, MN1
Obejero-Paz, CA1
Kuryshev, YA1
Brown, AM1
Erfurth, EM1
Holmer, H1
Nilsson, PG1
Kornhall, B1
Aessopos, A3
Farmakis, D3
Hatziliami, A1
Fragodimitri, C1
Karabatsos, F1
Joussef, J1
Mitilineou, E1
Diamanti-Kandaraki, E1
Meletis, J2
Karagiorga, M1
Borgna-Pignatti, C1
Rugolotto, S1
De Stefano, P1
Zhao, H1
Del Vecchio, GC1
Romeo, MA1
Forni, GL1
Gamberini, MR1
Ghilardi, R1
Piga, A1
Cnaan, A1
Tsironi, M2
Deftereos, S2
Andriopoulos, P2
Polonifi, K1
Moyssakis, I1
Pennell, DJ2
Martín, M1
Estornell, J1
Orero, M1
Pérez, JL1
Ridocci, F1
Martínez, V1
Tavecchia, L1
Masera, N1
Russo, P1
Cirò, A1
Vincenzi, A1
Vimercati, C1
Masera, G1
Kolnagou, A2
Economides, C1
Eracleous, E1
Kontoghiorghes, GJ2
Huang, YC1
Fabio, G1
Minonzio, F1
Delbini, P1
Bianchi, A1
Templin, C1
Pertschy, S1
Schaefer, A1
Tanner, MA1
Smith, GC1
Westwood, MA1
Agus, A1
Roughton, M1
Assomull, R1
Nair, SV1
Walker, JM1
Kondur, AK1
Li, T1
Vaitkevicius, P1
Afonso, L1
Bannerman, RM1
Keusch, G1
Kreimer-Birnbaum, M1
Vance, VK1
Vaughan, S1
Baudouy, P1
Lombrail, P1
Azancot, I1
Piekarski, A1
Martin, E1
Slama, R1
Nienhuis, AW2
Griffith, P1
Strawczynski, H1
Henry, W2
Borer, J1
Leon, M1
Anderson, WF1
Pisano, GF1
Binaghi, F1
Putzu, ML1
Bragotti, R1
Manconi, E1
Urgu, G1
Pitzus, F1
Hou, JW1
Wu, MH1
Lin, KH1
Lue, HC1
Wacker, P1
Halperin, DS1
Balmer-Ruedin, D1
Oberhansli, I1
Wyss, M1
Mariotti, E1
Agostini, A1
Angelucci, E1
Cesaroni, P1
Lucarelli, G1
Sgarbi, E1
Kelly, AL1
Rhodes, DA1
Roland, JM1
Schofield, P1
Cox, TM1
Young, N1
Sinclair, WP1
Afrooz, N1
de Montalembert, M1
Jan, D1
Clairicia, M1
Hannedouche, T1
Sidi, D1
Girot, R1
Tiede, R1
Sareen, S1
Singal, PK1
Freeman, AP1
Giles, RW1
Berdoukas, VA1
Talley, PA1
Murray, IP1
Rahko, PS1
Salerni, R1
Uretsky, BF1
Festa, RS1
Kanz, L1
Arnold, H1
Löhr, GW1
Mancuso, L1
Iacona, MA1
Marchi, S1
Rigano, P1
Geraci, E1
Seshadri, R1
Colebatch, JH1
Gordon, P1
Ekert, H1
Giorgio, AJ1
Lukens, JN1
Neuman, LA1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Iron-mediated Vascular Disease in Sickle Cell Disease.[NCT01239901]150 participants (Actual)Observational2009-12-31Completed
[NCT00000595]Phase 20 participants Interventional1978-01-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

4 reviews available for deferoxamine and Cardiac Failure

ArticleYear
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
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
Quantification of myocardial iron overload by cardiovascular magnetic resonance imaging T2* and review of the literature.
    Clinical cardiology, 2009, Volume: 32, Issue:6

    Topics: Animals; Cardiomyopathies; Deferoxamine; Early Diagnosis; Female; Heart Failure; Hemosiderosis; Huma

2009
Modern management of thalassemia.
    Pediatric annals, 1985, Volume: 14, Issue:9

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

1985

Trials

4 trials available for deferoxamine and Cardiac Failure

ArticleYear
Treatment of heart failure in adults with thalassemia major: response in patients randomised to deferoxamine with or without deferiprone.
    Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 2013, May-20, Volume: 15

    Topics: Adult; beta-Thalassemia; Deferiprone; Deferoxamine; Drug Therapy, Combination; Female; Heart Failure

2013
Cardiac iron removal and functional cardiac improvement by different iron chelation regimens in thalassemia major patients.
    Annals of hematology, 2012, Volume: 91, Issue:9

    Topics: Adult; Benzoates; beta-Thalassemia; Comorbidity; Deferasirox; Deferiprone; Deferoxamine; Drug Therap

2012
Effective combination therapy of deferiprone and deferoxamine for the rapid clearance of excess cardiac IRON and the prevention of heart disease in thalassemia. The Protocol of the International Committee on Oral Chelators.
    Hemoglobin, 2006, Volume: 30, Issue:2

    Topics: Administration, Oral; beta-Thalassemia; Cardiomyopathies; Chelation Therapy; Clinical Protocols; Com

2006
A randomized, placebo-controlled, double-blind trial of the effect of combined therapy with deferoxamine and deferiprone on myocardial iron in thalassemia major using cardiovascular magnetic resonance.
    Circulation, 2007, Apr-10, Volume: 115, Issue:14

    Topics: Adult; Agranulocytosis; Arthralgia; beta-Thalassemia; Chelation Therapy; Deferiprone; Deferoxamine;

2007

Other Studies

39 other studies available for deferoxamine and Cardiac Failure

ArticleYear
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
Catalytic iron mediated renal stress responses during experimental cardiorenal syndrome 1 ("CRS-1").
    Translational research : the journal of laboratory and clinical medicine, 2021, Volume: 237

    Topics: Animals; Biomarkers; Cardio-Renal Syndrome; Cell Line; Deferoxamine; Gene Expression Regulation; Hea

2021
Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report.
    Journal of medical case reports, 2018, Jan-26, Volume: 12, Issue:1

    Topics: Adult; Biopsy; Chelation Therapy; Deferoxamine; Echocardiography; Ferritins; Heart Failure; Heart Ve

2018
Impact of heart magnetic resonance imaging on chelation choices, compliance with treatment and risk of heart disease in patients with thalassaemia major.
    British journal of haematology, 2013, Volume: 163, Issue:3

    Topics: Adult; Area Under Curve; Arrhythmias, Cardiac; Benzoates; beta-Thalassemia; Chelation Therapy; Defer

2013
Successful Treatment of Iron-Overload Cardiomyopathy in Hereditary Hemochromatosis With Deferoxamine and Deferiprone.
    The Canadian journal of cardiology, 2016, Volume: 32, Issue:12

    Topics: Cardiomyopathies; Deferiprone; Deferoxamine; Ferritins; Heart Failure; Hemochromatosis; Hemochromato

2016
Downregulation of ferritin heavy chain increases labile iron pool, oxidative stress and cell death in cardiomyocytes.
    Journal of molecular and cellular cardiology, 2009, Volume: 46, Issue:1

    Topics: Animals; Antioxidants; Aorta; Apoferritins; Chelating Agents; Deferoxamine; Down-Regulation; Ferrocy

2009
[ERYTHROBLASTOPHTHISIS].
    Medizinische Klinik, 1964, Mar-20, Volume: 59

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

1964
Deferoxamine prevents cardiac hypertrophy and failure in the gerbil model of iron-induced cardiomyopathy.
    The Journal of laboratory and clinical medicine, 2003, Volume: 142, Issue:5

    Topics: Animals; Cardiomegaly; Cardiomyopathies; Deferoxamine; Female; Gerbillinae; Heart Failure; Iron; Iro

2003
Combined therapy with deferiprone and desferrioxamine successfully regresses severe heart failure in patients with beta-thalassemia major.
    Annals of hematology, 2004, Volume: 83, Issue:7

    Topics: Adult; beta-Thalassemia; Cardiovascular Agents; Deferiprone; Deferoxamine; Diabetes Complications; D

2004
Is growth hormone deficiency contributing to heart failure in patients with beta-thalassemia major?
    European journal of endocrinology, 2004, Volume: 151, Issue:2

    Topics: Adult; beta-Thalassemia; Cardiotonic Agents; Deferoxamine; Female; Heart Failure; Human Growth Hormo

2004
Cardiac status in well-treated patients with thalassemia major.
    European journal of haematology, 2004, Volume: 73, Issue:5

    Topics: Adolescent; Adult; beta-Thalassemia; Blood Transfusion; Cardiac Output; Child; Deferoxamine; Echocar

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
Reversal of heart failure in thalassemia major by combined chelation therapy: a case report.
    European journal of haematology, 2005, Volume: 74, Issue:1

    Topics: Adult; beta-Thalassemia; Deferiprone; Deferoxamine; Drug Synergism; Drug Therapy, Combination; Heart

2005
Transfusional hemosiderosis and combined chelation therapy in sickle thalassemia.
    European journal of haematology, 2005, Volume: 75, Issue:4

    Topics: Adult; Anemia, Sickle Cell; beta-Thalassemia; Blood Transfusion; Chelation Therapy; Deferiprone; Def

2005
[Magnetic resonance imaging evidence of the effectiveness of combination chelation therapy in iron overload cardiomyopathy].
    Revista espanola de cardiologia, 2006, Volume: 59, Issue:1

    Topics: Adult; beta-Thalassemia; Chelation Therapy; Deferiprone; Deferoxamine; Heart Failure; Humans; Iron C

2006
Successful recovery of acute hemosiderotic heart failure in beta-thalassemia major treated with a combined regimen of desferrioxamine and deferiprone.
    Haematologica, 2006, Volume: 91, Issue:6 Suppl

    Topics: Adult; beta-Thalassemia; Deferiprone; Deferoxamine; Drug Therapy, Combination; Heart Failure; Hemosi

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
Regression of myocardial dysfunction after switching from desferrioxamine to deferiprone therapy in beta-thalassemia major patients.
    Hemoglobin, 2006, Volume: 30, Issue:2

    Topics: Adolescent; Adult; beta-Thalassemia; Cardiomegaly; Cardiomyopathies; Chelation Therapy; Cohort Studi

2006
Reversal of cardiac complications by deferiprone and deferoxamine combination therapy in a patient affected by a severe type of juvenile hemochromatosis (JH).
    Blood, 2007, Jan-01, Volume: 109, Issue:1

    Topics: Adult; Amino Acid Substitution; Antimicrobial Cationic Peptides; Atrial Fibrillation; Chelation Ther

2007
Cardiac hemochromatosis.
    International journal of cardiology, 2007, Apr-04, Volume: 116, Issue:3

    Topics: Deferoxamine; Erythrocyte Transfusion; Fatal Outcome; Female; Heart Diseases; Heart Failure; Hemochr

2007
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
[Adiastole caused by a secondary cardiac hemochromatosis. Successful treatment with an iron chelating agent].
    Archives des maladies du coeur et des vaisseaux, 1983, Volume: 76, Issue:10

    Topics: Adult; Arrhythmias, Cardiac; Cardiomyopathy, Dilated; Deferoxamine; Diastole; Echocardiography; Elec

1983
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
[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
Prognostic significance of left ventricular diastolic indexes in beta-thalassemia major.
    Archives of pediatrics & adolescent medicine, 1994, Volume: 148, Issue:8

    Topics: Adolescent; Adult; Age Factors; beta-Thalassemia; Child; Child, Preschool; Deferoxamine; Diastole; E

1994
Regression of cardiac insufficiency after ambulatory intravenous deferoxamine in thalassemia major.
    Chest, 1993, Volume: 103, Issue:4

    Topics: Adult; Ambulatory Care; beta-Thalassemia; Deferoxamine; Echocardiography; Heart Failure; Humans; Inf

1993
Cardiac study by dobutamine stress echocardiography in thalassemic patients.
    Bone marrow transplantation, 1993, Volume: 12 Suppl 1

    Topics: Adolescent; Adult; beta-Thalassemia; Chelation Therapy; Child; Combined Modality Therapy; Deferoxami

1993
Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage disease.
    QJM : monthly journal of the Association of Physicians, 1998, Volume: 91, Issue:9

    Topics: Adolescent; Adult; Age of Onset; Chelating Agents; Deferoxamine; Endocrine System Diseases; Female;

1998
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
Idiopathic hemochromatosis: case report of a patient presenting with neurologic symptoms.
    Journal of the American Geriatrics Society, 1977, Volume: 25, Issue:7

    Topics: Aged; Deferoxamine; Diabetes Mellitus; Female; Heart Failure; Hemochromatosis; Humans; Iron; Liver C

1977
[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
Transferrin delays oxygen radical induced cardiac-contractile failure.
    Canadian journal of physiology and pharmacology, 1990, Volume: 68, Issue:4

    Topics: Animals; Basement Membrane; Deferoxamine; Free Radicals; Heart Failure; Lipid Peroxidation; Male; Ma

1990
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
Successful reversal by chelation therapy of congestive cardiomyopathy due to iron overload.
    Journal of the American College of Cardiology, 1986, Volume: 8, Issue:2

    Topics: Adult; Anemia, Macrocytic; Anemia, Megaloblastic; Deferoxamine; Diabetes Complications; Echocardiogr

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
[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
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
Primary hemochromatosis: easily missed cause of cirrhosis, diabetes and heart failure.
    Geriatrics, 1973, Volume: 28, Issue:4

    Topics: Age Factors; Aged; Blood Cell Count; Bloodletting; Deferoxamine; Diabetes Mellitus; Female; Heart Fa

1973
EXcretion and distribution of iron during chronic deferoxamine therapy.
    Blood, 1971, Volume: 38, Issue:5

    Topics: Anemia, Aplastic; Bone Marrow; Bone Marrow Examination; Child; Chromium Isotopes; Deferoxamine; Foli

1971