arginine and Thalassemia

arginine has been researched along with Thalassemia in 18 studies

Research

Studies (18)

TimeframeStudies, this research(%)All Research%
pre-19909 (50.00)18.7374
1990's3 (16.67)18.2507
2000's4 (22.22)29.6817
2010's2 (11.11)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Al-Malki, AL; Choudhry, H; Helmi, N; Kumosani, AT; Kumosani, TA; Moselhy, SS; Qari, M1
Hassell, K; Kim, HY; Klings, ES; Kuypers, FA; Kwiatkowski, JL; Larkin, S; Morris, CR; Neufeld, EJ; Olivieri, NF; Porter, JB; Suh, JH; Sweeters, N; Taher, A; Thompson, AA; Trachtenberg, F; Vichinsky, EP; Virzi, L; Wood, J1
Morris, CR1
Caruso-Nicoletti, M; De Sanctis, V; Galati, MC; Guardabasso, V; La Rosa, C; Mancuso, M; Mangiagli, A1
Kato, GJ; Kuypers, FA; Larkin, S; Lavrisha, L; Morris, CR; Singer, T; Vichinsky, EP1
Balduini, CL; De Candia, E; Savoia, A1
Atti, G; Bagni, B; Capra, L; Cavallini, AR; de Sanctis, V; Lucci, M; Vullo, C; Zucchi, F1
Olivieri, NF; Sher, GD1
Andò, S; Brancati, C; Bria, M; Caracciolo, M; DeLuca, G; Giorno, A; Lanzino, M; Maggiolini, M; Marsico, S; Salerno, M1
Al-Khider, A; Bayoumi, RA; Dawodu, A; Fisher, CA; Fitches, A; Fitzgerald, P; Old, JM; Qureshi, MM; Riou, J1
Changloah, L; Flatz, G; Matragoon, S; Sanguansermsri, T1
Gugler, E; Hirt, A; Imbach, P; Molinari, B; Tönz, O; Zuppinger, K; Zurbrügg, RP1
Alberti, R; Borghesi, V; Martinucci, M; Tentori, L1
Cash, FE; Goossens, M; Liebhaber, SA; Monplaisir, N1
Baklouti, F; Baudin, V; Delaunay, J; Wajcman, H1
Atti, G; Bagni, B; Borgatti, L; De Sanctis, V; Gamberini, MR; Vullo, C1
Kass, L1
Brimhall, B; Gustavson, LP; Haggard, ME; Jones, RT; Schneider, RG1

Reviews

1 review(s) available for arginine and Thalassemia

ArticleYear
Mechanisms of vasculopathy in sickle cell disease and thalassemia.
    Hematology. American Society of Hematology. Education Program, 2008

    Topics: Anemia, Sickle Cell; Apolipoproteins; Arginine; Biological Transport; Endothelium, Vascular; Hemolysis; Humans; Inflammation; Kidney Diseases; Nitric Oxide; Nitric Oxide Synthase; Oxidative Stress; Reperfusion Injury; Thalassemia

2008

Trials

1 trial(s) available for arginine and Thalassemia

ArticleYear
GH secretion in thalassemia patients with short stature.
    Hormone research, 1995, Volume: 44, Issue:4

    Topics: Adolescent; Age Determination by Skeleton; Arginine; Body Height; Body Mass Index; Child; Female; Growth Disorders; Growth Hormone; Humans; Insulin-Like Growth Factor I; Male; Parasympathomimetics; Pyridostigmine Bromide; Thalassemia

1995

Other Studies

16 other study(ies) available for arginine and Thalassemia

ArticleYear
Association of serum asymmetric dimethyl-arginine and troponin I levels as a risk of myocardial infarction in thalassemia.
    African health sciences, 2018, Volume: 18, Issue:3

    Topics: Arginine; Biomarkers; Case-Control Studies; Creatine Kinase, MB Form; Humans; L-Lactate Dehydrogenase; Myocardial Infarction; Risk Factors; Thalassemia; Troponin I

2018
Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia.
    British journal of haematology, 2015, Volume: 169, Issue:6

    Topics: Adult; Arginase; Arginine; Case-Control Studies; Cross-Sectional Studies; Echocardiography, Doppler; Female; Humans; Hypertension, Pulmonary; Male; Middle Aged; Thalassemia; Young Adult

2015
Growth hormone secretion in adult patients with thalassaemia.
    Clinical endocrinology, 2005, Volume: 62, Issue:6

    Topics: Adolescent; Adult; Age of Onset; Arginine; Female; Ferritins; Growth Hormone; Growth Hormone-Releasing Hormone; Humans; Insulin-Like Growth Factor I; Lipids; Male; Thalassemia

2005
Hemolysis-associated pulmonary hypertension in thalassemia.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: alpha-Thalassemia; Arginase; Arginine; Endothelium, Vascular; Erythrocytes; Hemoglobin E; Hemolysis; Humans; Hypertension, Pulmonary; Nitric Oxide; Ornithine; Thalassemia; Tricuspid Valve

2005
Why the disorder induced by GATA1 Arg216Gln mutation should be called "X-linked thrombocytopenia with thalassemia" rather than "X-linked gray platelet syndrome".
    Blood, 2007, Oct-01, Volume: 110, Issue:7

    Topics: Arginine; Blood Platelets; GATA1 Transcription Factor; Genes, X-Linked; Glutamine; Humans; Mutation; Syndrome; Terminology as Topic; Thalassemia; Thrombocytopenia

2007
[Evaluation of alpha and beta pancreatic function in beta-thalassemia major].
    La Radiologia medica, 1980, Volume: 66, Issue:11

    Topics: Adolescent; Adult; Arginine; Child; Glucagon; Glucose Tolerance Test; Humans; Insulin; Pancreatic Function Tests; Thalassemia

1980
Rapid healing of chronic leg ulcers during arginine butyrate therapy in patients with sickle cell disease and thalassemia.
    Blood, 1994, Oct-01, Volume: 84, Issue:7

    Topics: Adult; Anemia, Sickle Cell; Arginine; Butyrates; Female; Hemoglobins, Abnormal; Humans; Leg Ulcer; Thalassemia

1994
The association of Hb Khartoum [beta124(H2)Pro-->Arg] with gamma+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese family.
    Hemoglobin, 1999, Volume: 23, Issue:1

    Topics: Adult; Arginine; Child; Child, Preschool; Erythroblastosis, Fetal; Female; Hemoglobins, Abnormal; Humans; Infant; Infant, Newborn; Male; Point Mutation; Proline; Sudan; Thalassemia

1999
Hemoglobin Suan-Dok (alpha 2 109 (G16) Leu replaced by Arg beta 2): an unstable variant associated with alpha-thalassemia.
    Hemoglobin, 1979, Volume: 3, Issue:2-3

    Topics: Adult; Amino Acids; Arginine; Child; Child, Preschool; Female; Globins; Hemoglobins, Abnormal; Humans; Leucine; Male; Peptide Fragments; Reticulocytes; Thailand; 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 1; Female; Glucose Tolerance Test; Growth Hormone; Hemochromatosis; Humans; Insulin; Iron; Male; Thalassemia; Transfusion Reaction

1979
Hb A2-Adria (delta 51 Pro yield Arg (D2)): a new delta-chain variant found in association with beta-thalassemia.
    Hemoglobin, 1978, Volume: 2, Issue:2

    Topics: Arginine; Child; Genetic Variation; Hemoglobin A; Hemoglobins; Humans; Italy; Male; Peptides; Proline; Thalassemia

1978
Locus assignment of two alpha-globin structural mutants from the Caribbean basin: alpha Fort de France (alpha 45 Arg) and alpha Spanish Town (alpha 27 Val).
    Blood, 1989, Aug-01, Volume: 74, Issue:2

    Topics: Amino Acid Sequence; Arginine; Genes; Globins; Humans; Mutation; Protein Biosynthesis; RNA, Messenger; Thalassemia; Valine; West Indies

1989
Hemoglobin Aichi [alpha 50(CE8)His----Arg] in a French Caucasian patient.
    Hemoglobin, 1987, Volume: 11, Issue:2

    Topics: Adult; Amino Acids; Arginine; Chromatography, High Pressure Liquid; Female; France; Hemoglobins, Abnormal; Histamine; Humans; Isoelectric Focusing; Thalassemia

1987
Alpha and beta cell evaluation in patients with thalassaemia intermedia and iron overload.
    Postgraduate medical journal, 1985, Volume: 61, Issue:721

    Topics: Adult; Arginine; Blood Glucose; Female; Ferritins; Glucagon; Glucose Tolerance Test; Humans; Insulin; Iron; Islets of Langerhans; Male; Middle Aged; Thalassemia

1985
Metachromatic staining of basic nucleoproteins in chronic erythremic myelosis.
    American journal of clinical pathology, 1974, Volume: 62, Issue:1

    Topics: Anemia, Hemolytic, Autoimmune; Anemia, Pernicious; Arginine; Bone Marrow; Bone Marrow Cells; Cell Nucleus; Chromatography, Paper; Chronic Disease; Histocytochemistry; Humans; Leukemia, Erythroblastic, Acute; Nucleoproteins; Osteoporosis; Staining and Labeling; Thalassemia

1974
Genetic haemoglobin abnormalities in about 9000 Black and 7000 White newborns; haemoglobin F Dickinson (Agamma97His-Arg), a new variant.
    British journal of haematology, 1974, Volume: 28, Issue:4

    Topics: Amino Acid Sequence; Amino Acids; Arginine; Black People; Electrophoresis; Globins; Hemoglobin C; Hemoglobin C Disease; Hemoglobin, Sickle; Hemoglobinopathies; Hemoglobins, Abnormal; Histamine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Sickle Cell Trait; Thalassemia; White People

1974
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