glutamic acid and HbS Disease

glutamic acid has been researched along with HbS Disease 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 HbS Disease

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 HbS Disease

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