glutamic acid and Anemia, Sickle Cell

glutamic acid has been researched along with Anemia, Sickle Cell in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Becchi, M; Francina, A; Joly, P; Préhu, C; Riou, J; Wajcman, H; Zanella-Cleon, I1
Brown, M; Duckworth, L; Froyen, M; Gauger, C; Kissoon, N; Murphy, S; Sandler, E; Sullivan, KJ1
Ames, B; Bland, DA; Hagar, W; Klings, ES; Kuypers, FA; Larkin, S; Morris, CR; Shigenaga, M; Steinberg, MH; Suh, JH; Vichinsky, EP1
Clemente, R; Mendelowitsch, A; Sekhar, LN; Shuaib, A1
Akiyama, DS; Niihara, Y; Tanaka, KR; Zerez, CR1
Ellory, JC; Gibson, JS; Kiessling, K; Roberts, N1

Trials

1 trial(s) available for glutamic acid and Anemia, Sickle Cell

ArticleYear
Effect of oral arginine supplementation on exhaled nitric oxide concentration in sickle cell anemia and acute chest syndrome.
    Journal of pediatric hematology/oncology, 2010, Volume: 32, Issue:7

    Topics: Acute Chest Syndrome; Acute Disease; Administration, Oral; Adolescent; Anemia, Sickle Cell; Arginine; Aspartic Acid; Breath Tests; Child; Citrulline; Female; Glutamic Acid; Humans; Male; Nitrates; Nitric Oxide; Nitrites; Ornithine; Young Adult

2010

Other Studies

5 other study(ies) available for glutamic acid and Anemia, Sickle Cell

ArticleYear
Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].
    Hemoglobin, 2009, Volume: 33, Issue:3

    Topics: Anemia, Sickle Cell; beta-Globins; Chromatography, Liquid; Female; Glutamic Acid; Hemoglobin, Sickle; Hemoglobins, Abnormal; Humans; Lysine; Mass Spectrometry; Middle Aged; Mutation; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Threonine; Valine

2009
Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease.
    Blood, 2008, Jan-01, Volume: 111, Issue:1

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Echinococcosis, Pulmonary; Erythrocytes; Female; Glutamic Acid; Glutamine; Hemolysis; Humans; Hydrogen-Ion Concentration; Male; NADP; Nitric Oxide; Oxidation-Reduction; Tricuspid Valve Insufficiency

2008
EC-IC bypass improves chronic ischemia in a patient with moyamoya disease secondary to sickle cell disease: an in vivo microdialysis study.
    Neurological research, 1997, Volume: 19, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Brain Ischemia; Cerebral Revascularization; Collateral Circulation; Extracellular Space; Glutamic Acid; Hemiplegia; Humans; Hydrogen-Ion Concentration; Lactates; Magnetic Resonance Angiography; Male; Microdialysis; Moyamoya Disease

1997
Increased red cell glutamine availability in sickle cell anemia: demonstration of increased active transport, affinity, and increased glutamate level in intact red cells.
    The Journal of laboratory and clinical medicine, 1997, Volume: 130, Issue:1

    Topics: Anemia, Sickle Cell; Biological Transport, Active; Erythrocytes; Glutamic Acid; Glutamine; Humans; Kinetics; NAD

1997
A comparison in normal individuals and sickle cell patients of reduced glutathione precursors and their transport between plasma and red cells.
    The hematology journal : the official journal of the European Haematology Association, 2000, Volume: 1, Issue:4

    Topics: Adult; Amino Acid Transport System ASC; Amino Acid Transport System L; Anemia, Sickle Cell; Biological Transport; Carbon Monoxide; Cysteine; Enzyme Inhibitors; Erythrocytes; Female; Glutamic Acid; Glutamine; Glutathione; Glycine; Humans; Male; Middle Aged; Oxygen; Protein Kinase Inhibitors; Protein Kinases; Serine; Staurosporine

2000