aspartic acid has been researched along with HbS Disease in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (42.86) | 18.7374 |
1990's | 2 (28.57) | 18.2507 |
2000's | 1 (14.29) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brown, M; Duckworth, L; Froyen, M; Gauger, C; Kissoon, N; Murphy, S; Sandler, E; Sullivan, KJ | 1 |
Ogg, RJ; Steen, RG | 1 |
Badens, C; Bardakdjian-Michau, J; BĂ©vier, A; Ducrocq, R; Elion, J; Leneveu, A; Maier-Redelsperger, M | 1 |
Bogdan, AR; Gusnard, DA; Leigh, JS; Ohene-Frempong, K; Wang, Z; Zimmerman, RA | 1 |
Fales, FW; Grush, OC; Sophianopoulos, AJ; Sophianopoulos, JA; Wilson, JS | 1 |
Beresford, CH; Clegg, JB; Weatherall, DJ | 1 |
Gallo, E; Konotey-Ahulu, FI; Lehmann, H; Ringelhann, B | 1 |
1 trial(s) available for aspartic acid and HbS Disease
Article | Year |
---|---|
Effect of oral arginine supplementation on exhaled nitric oxide concentration in sickle cell anemia and acute chest syndrome.
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 |
6 other study(ies) available for aspartic acid and HbS Disease
Article | Year |
---|---|
Abnormally high levels of brain N-acetylaspartate in children with sickle cell disease.
Topics: Adolescent; Anemia, Sickle Cell; Aspartic Acid; Basal Ganglia; Brain; Case-Control Studies; Child; Choline; Female; Humans; Magnetic Resonance Spectroscopy; Male; Osmolar Concentration | 2005 |
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell disease.
Topics: Anemia, Sickle Cell; Aspartic Acid; Chromatography, High Pressure Liquid; Genetic Carrier Screening; Glycine; Hemoglobin, Sickle; Hemoglobins, Abnormal; Humans; Infant, Newborn; Isoelectric Focusing; Neonatal Screening; Point Mutation | 1998 |
Investigation of stroke in sickle cell disease by 1H nuclear magnetic resonance spectroscopy.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Aspartic Acid; Atrophy; Brain; Brain Ischemia; Cerebral Infarction; Cerebrovascular Disorders; Child; Choline; Creatine; Female; Frontal Lobe; Humans; Hydrogen; Lactates; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Phosphocreatine | 1992 |
Two new antisickling agents and the use of amino acid salts.
Topics: Anemia, Sickle Cell; Arginine; Aspartic Acid; Drug Synergism; Edetic Acid; Glucose; Glutamates; Hemoglobins, Abnormal; Homozygote; Humans; Hydrogen-Ion Concentration; Lysine; Osmolar Concentration | 1974 |
Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.
Topics: Alanine; Amino Acid Sequence; Anemia, Sickle Cell; Aspartic Acid; Blood Protein Electrophoresis; Chromatography; Electrophoresis, Starch Gel; Hemoglobins, Abnormal; Heterozygote; Humans; Infant; Male; Methods; Peptides; Trypsin | 1972 |
Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem.
Topics: Aged; Amino Acid Sequence; Amino Acids; Anemia, Sickle Cell; Asparagine; Aspartic Acid; Crossing Over, Genetic; Electrophoresis; Hemoglobins, Abnormal; Humans; Male | 1968 |