arginine and Anemia, Cooley's

arginine has been researched along with Anemia, Cooley's in 24 studies

Research

Studies (24)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	12 (50.00)	18.2507
2000's	3 (12.50)	29.6817
2010's	8 (33.33)	24.3611
2020's	1 (4.17)	2.80

Authors

Authors	Studies
Aliberti, L; Ambrosio, MR; Bondanelli, M; Dassie, F; Fortini, M; Gagliardi, I; Gamberini, MR; Maffei, P; Mungari, R; Putti, MC; Zatelli, MC	1
Eker, I; Gursel, O; Ileri, T; Kurekci, AE; Sertoglu, E; Tapan, S; Taşçılar, E; Uysal, Z	1
Ishikawa, H; Izumikawa, K; Simpson, RJ; Takahashi, N	1
Dadheech, S; Hussien, MD; Jain, S; Jyothy, A; Munshi, A; Rao, AV; Shaheen, U	1
Amr, D; Ibrahim, B; Mohamed, el-S; Mokhtar, M; Noha, el-K	1
Coates, TD; Detterich, J; Harmatz, P; Meloni, A; Pepe, A; Wood, JC	1
Amodeo, G; Girelli, G; Lauri, C; Monti, S; Pascucci, C; Poggi, M; Pugliese, P; Toscano, V	1
Biemond, BJ; Brandjes, DP; Duits, AJ; Landburg, PP; Muskiet, FA; Schnog, JB; Teerlink, T	1
Grassi, G; Mancia, G; Mariani, R; Masera, G; Masera, N; Perotti, M; Perra, S; Pincelli, AI; Piperno, A; Tavecchia, L	1
Morris, CR; Singer, ST; Walters, MC	1
Argento, C; Cappellini, MD; Carnelli, V; Cattaneo, A; Cavagnini, F; D'Angelo, E; Danesi, L; Mirra, N; Pecori Giraldi, F; Scacchi, M; Valassi, E; Zanaboni, L	1
Dresner-Pollak, R; Glaser, B; Goldfarb, AW; Vidergor, G	1
Dover, GJ; Faller, DV; Ginder, GD; Olivieri, NF; Perrine, SP; Vichinsky, EP	1
Bunn, HF	1
Cai, SP; Dover, GH; Faller, DV; Ginder, GD; Ikuta, T; Olivieri, NF; Perrine, SP; Vichinsky, EP; Witkowska, HE	1
Dover, GJ; Ginder, GD; Little, J; Olivieri, NF; Sher, GD; Yang, S	1
Lal, A; Marwaha, RK	1
Chalevelakis, G; Yalouris, AG	1
Arjona, SN; Eloy-Garcia, JM; Gu, LH; Huisman, TH; Smetanina, NS	1
alSalmi, I; Asfour, M; el Banna, N; Soliman, AT	1
Chui, DH; Eng, B; Fernandes, BJ; Patterson, M; Waye, JS	1
Fibach, E; Friedberg, A; Goldfarb, A; Rachmilewitz, E; Rund, D	1
Agarwal, S; Agarwal, SS; Gupta, UR; Hattori, Y	1
Cho, HI; Hattori, Y; Kim, BK; Kim, SI; Lee, NY; Ohba, Y	1

Reviews

2 review(s) available for arginine and Anemia, Cooley's

Article	Year
Modulating the expression of Chtop, a versatile regulator of gene-specific transcription and mRNA export. RNA biology, 2018, Volume: 15, Issue:7 Topics: Animals; Arginine; beta-Thalassemia; Glioblastoma; Humans; Introns; Methylation; Mice; Nonsense Mediated mRNA Decay; Nuclear Proteins; Protein-Arginine N-Methyltransferases; Repressor Proteins; RNA Splicing; RNA, Messenger; Transcription Factors; Transcription, Genetic	2018
Clinical hemoglobinopathies: iron, lungs and new blood. Current opinion in hematology, 2006, Volume: 13, Issue:6 Topics: Anemia, Sickle Cell; Arginine; beta-Thalassemia; Child; Hematopoietic Stem Cell Transplantation; Humans; Hypertension, Pulmonary; Iron Chelating Agents; Iron Overload; Prognosis	2006

Article

Year

Modulating the expression of Chtop, a versatile regulator of gene-specific transcription and mRNA export.

RNA biology, 2018, Volume: 15, Issue:7

Topics: Animals; Arginine; beta-Thalassemia; Glioblastoma; Humans; Introns; Methylation; Mice; Nonsense Mediated mRNA Decay; Nuclear Proteins; Protein-Arginine N-Methyltransferases; Repressor Proteins; RNA Splicing; RNA, Messenger; Transcription Factors; Transcription, Genetic

2018

Clinical hemoglobinopathies: iron, lungs and new blood.

Current opinion in hematology, 2006, Volume: 13, Issue:6

Topics: Anemia, Sickle Cell; Arginine; beta-Thalassemia; Child; Hematopoietic Stem Cell Transplantation; Humans; Hypertension, Pulmonary; Iron Chelating Agents; Iron Overload; Prognosis

2006

Trials

1 trial(s) available for arginine and Anemia, Cooley's

Article	Year
A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders. The New England journal of medicine, 1993, Jan-14, Volume: 328, Issue:2 Topics: Adolescent; Adult; Anemia, Sickle Cell; Arginine; beta-Thalassemia; Butyrates; Child; Child, Preschool; Female; Fetal Hemoglobin; Globins; Humans; Infusions, Intravenous; Male; RNA, Messenger	1993

Other Studies

21 other study(ies) available for arginine and Anemia, Cooley's

Article	Year
GH/IGF-1 axis in a large cohort of ß-thalassemia major adult patients: a cross-sectional study. Journal of endocrinological investigation, 2022, Volume: 45, Issue:7 Topics: Adult; Arginine; beta-Thalassemia; Cross-Sectional Studies; Human Growth Hormone; Humans; Insulin-Like Growth Factor I; Lipids; Male; Middle Aged	2022
Elevated plasma asymmetric dimethylarginine levels in children with beta-thalassemia major may be an early marker for endothelial dysfunction. Hematology (Amsterdam, Netherlands), 2018, Volume: 23, Issue:5 Topics: Adolescent; Arginine; beta-Thalassemia; Biomarkers; C-Reactive Protein; Child; Child, Preschool; Endothelium; Female; Humans; Intercellular Adhesion Molecule-1; Male; P-Selectin; Serum Amyloid P-Component; Vascular Cell Adhesion Molecule-1	2018
Three most common nonsynonymous UGT1A62 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients. Gene, 2013, Dec-01, Volume: 531, Issue:2* Topics: Adolescent; Alanine; Amino Acid Substitution; Arginine; beta-Thalassemia; Child; Child, Preschool; Deferiprone; Female; Gene Frequency; Genetic Association Studies; Glucuronosyltransferase; Humans; Iron Chelating Agents; Iron Overload; Isoenzymes; Male; Mutation, Missense; Polymorphism, Single Nucleotide; Pyridones; Serine; Threonine; Treatment Outcome	2013
Asymmetric dimethylarginine levels in children with β-thalassemia and their correlations to tricuspid regurgitant jet velocity. Pediatric blood & cancer, 2014, Volume: 61, Issue:9 Topics: Adolescent; Arginine; beta-Thalassemia; Case-Control Studies; Child; Echocardiography, Doppler; Female; Follow-Up Studies; Humans; Hypertension, Pulmonary; Male; Prognosis; Risk Factors; Tricuspid Valve Insufficiency	2014
Pulmonary hypertension in well-transfused thalassemia major patients. Blood cells, molecules & diseases, 2015, Volume: 54, Issue:2 Topics: Adolescent; Adult; Arginine; beta-Thalassemia; Erythrocyte Transfusion; Female; Hemolysis; Humans; Hypertension, Pulmonary; Iron; Iron Overload; Male; Risk Factors; Tricuspid Valve Insufficiency; Ultrasonography	2015
Prevalence of growth hormone deficiency in adult polytransfused β-thalassemia patients and correlation with transfusional and chelation parameters. Journal of endocrinological investigation, 2010, Volume: 33, Issue:8 Topics: Absorptiometry, Photon; Adolescent; Adult; Arginine; beta-Thalassemia; Blood Transfusion; Chelation Therapy; Female; Growth Hormone; Growth Hormone-Releasing Hormone; Humans; Male	2010
Plasma asymmetric dimethylarginine concentrations in sickle cell disease are related to the hemolytic phenotype. Blood cells, molecules & diseases, 2010, Apr-15, Volume: 44, Issue:4 Topics: Adult; Albuminuria; Anemia, Sickle Cell; Arginine; beta-Thalassemia; Cholelithiasis; Female; Hemolysis; Humans; Hypertension, Pulmonary; Leg Ulcer; Male; Middle Aged; Nitric Oxide; Osteonecrosis; Phenotype; Priapism; Retinal Diseases; Sickle Cell Trait; Young Adult	2010
GH deficiency in adult B-thalassemia major patients and its relationship with IGF-1 production. Pediatric endocrinology reviews : PER, 2011, Volume: 8 Suppl 2 Topics: Adult; Age Factors; Arginine; beta-Thalassemia; Calcification, Physiologic; Cohort Studies; Female; Growth Disorders; Growth Hormone-Releasing Hormone; Hepatitis C; Human Growth Hormone; Humans; Insulin-Like Growth Factor I; Iron Overload; Laron Syndrome; Male; Prevalence; Young Adult	2011
Growth hormone deficiency (GHD) in adult thalassaemic patients. Clinical endocrinology, 2007, Volume: 67, Issue:5 Topics: Adult; Arginine; beta-Thalassemia; Butyrylcholinesterase; Cross-Sectional Studies; Female; Ferritins; Growth Hormone; Growth Hormone-Releasing Hormone; Humans; Hydrocortisone; Insulin-Like Growth Factor I; Linear Models; Male; Prevalence	2007
Growth hormone reserve in adult beta thalassemia patients. Endocrine, 2007, Volume: 31, Issue:1 Topics: Adult; Arginine; beta-Thalassemia; Case-Control Studies; Female; Growth Hormone; Growth Hormone-Releasing Hormone; Humans; Insulin-Like Growth Factor Binding Protein 3; Insulin-Like Growth Factor I; Male; Middle Aged	2007
Butyrate derivatives. New agents for stimulating fetal globin production in the beta-globin disorders. The American journal of pediatric hematology/oncology, 1994, Volume: 16, Issue:1 Topics: Adolescent; Adult; Amides; Anemia, Sickle Cell; Animals; Arginine; beta-Thalassemia; Butyrates; Child; Child, Preschool; Fetal Hemoglobin; Globins; Humans; Promoter Regions, Genetic	1994
Reversing ontogeny. The New England journal of medicine, 1993, Jan-14, Volume: 328, Issue:2 Topics: Anemia, Sickle Cell; Arginine; beta-Thalassemia; Butyrates; Fetal Hemoglobin; Globins; Humans; Hydroxyurea	1993
Extended therapy with intravenous arginine butyrate in patients with beta-hemoglobinopathies. The New England journal of medicine, 1995, Jun-15, Volume: 332, Issue:24 Topics: Adolescent; Adult; Anemia, Sickle Cell; Arginine; beta-Thalassemia; Biomarkers; Butyrates; Child; Child, Preschool; Female; Hemoglobins; Humans; Infusions, Intravenous; Male	1995
Present status of hemoglobinopathies in India. Indian pediatrics, 1994, Volume: 31, Issue:3 Topics: Administration, Oral; Arginine; beta-Thalassemia; Butyrates; Chelating Agents; Chelation Therapy; Genetic Therapy; Humans; India	1994
Haem administration in myelodysplastic syndromes: a possible mechanism of action. European journal of haematology, 1993, Volume: 51, Issue:1 Topics: alpha-Thalassemia; Arginine; beta-Thalassemia; Globins; Heme; Humans; Myelodysplastic Syndromes; Reticulocytes	1993
The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon ( = arginine) at the 5' end of the second exon. British journal of haematology, 1996, Volume: 93, Issue:4 Topics: Arginine; Base Sequence; beta-Thalassemia; Child; DNA Transposable Elements; Exons; Female; Frameshift Mutation; Hemoglobin A2; Hemoglobins; Humans; Molecular Sequence Data; Pedigree; RNA, Messenger	1996
Insulin and glucagon responses to provocation with glucose and arginine in prepubertal children with thalassemia major before and after long-term blood transfusion. Journal of tropical pediatrics, 1996, Volume: 42, Issue:5 Topics: Arginine; beta-Thalassemia; Blood Transfusion; Child, Preschool; Female; Glucagon; Glucose Tolerance Test; Humans; Infant; Insulin; Male; Prospective Studies; Time Factors; Transfusion Reaction	1996
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)]. Hemoglobin, 1998, Volume: 22, Issue:1 Topics: Adult; Amino Acid Substitution; Arginine; beta-Thalassemia; Female; Glycine; Humans; Introns; Jews; Middle Aged; Point Mutation	1998
Heme arginate therapy for beta thalassemia: in vitro versus in vivo effects. Acta haematologica, 1998, Volume: 100, Issue:2 Topics: Adult; Arginine; beta-Thalassemia; Cells, Cultured; Female; Heme; Humans; Infusions, Intravenous; Male; Treatment Outcome	1998
A novel Indian beta-thalassemia mutation: Hb Lucknow [beta8(A5)Lys-->Arg]]. Hemoglobin, 1999, Volume: 23, Issue:3 Topics: Adolescent; Arginine; Base Sequence; beta-Thalassemia; Globins; Hematologic Tests; Hemoglobins; Hemoglobins, Abnormal; Hepatitis, Viral, Human; Humans; India; Lysine; Male; Pedigree; Phenotype; Point Mutation	1999
A family case of beta-thalassemia minor and hemoglobin Queens: alpha 34 (B15) Leu-Arg. Journal of Korean medical science, 1992, Volume: 7, Issue:4 Topics: Adult; Arginine; beta-Thalassemia; Female; Hemoglobins, Abnormal; Humans; Korea; Leucine; Male; Pedigree	1992