Page last updated: 2024-08-17

aspartic acid and HbS Disease

aspartic acid has been researched along with HbS Disease in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's2 (28.57)18.2507
2000's1 (14.29)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brown, M; Duckworth, L; Froyen, M; Gauger, C; Kissoon, N; Murphy, S; Sandler, E; Sullivan, KJ1
Ogg, RJ; Steen, RG1
Badens, C; Bardakdjian-Michau, J; BĂ©vier, A; Ducrocq, R; Elion, J; Leneveu, A; Maier-Redelsperger, M1
Bogdan, AR; Gusnard, DA; Leigh, JS; Ohene-Frempong, K; Wang, Z; Zimmerman, RA1
Fales, FW; Grush, OC; Sophianopoulos, AJ; Sophianopoulos, JA; Wilson, JS1
Beresford, CH; Clegg, JB; Weatherall, DJ1
Gallo, E; Konotey-Ahulu, FI; Lehmann, H; Ringelhann, B1

Trials

1 trial(s) available for aspartic 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

6 other study(ies) available for aspartic acid and HbS Disease

ArticleYear
Abnormally high levels of brain N-acetylaspartate in children with sickle cell disease.
    AJNR. American journal of neuroradiology, 2005, Volume: 26, Issue:3

    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.
    Journal of medical screening, 1998, Volume: 5, Issue:1

    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.
    Neuroradiology, 1992, Volume: 35, Issue:1

    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.
    Clinical biochemistry, 1974, Volume: 7, Issue:2

    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.
    Journal of medical genetics, 1972, Volume: 9, Issue:2

    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.
    Journal of medical genetics, 1968, Volume: 5, Issue:2

    Topics: Aged; Amino Acid Sequence; Amino Acids; Anemia, Sickle Cell; Asparagine; Aspartic Acid; Crossing Over, Genetic; Electrophoresis; Hemoglobins, Abnormal; Humans; Male

1968