aspartic acid has been researched along with BH4 Deficiency in 21 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 14 (66.67) | 18.7374 |
1990's | 5 (23.81) | 18.2507 |
2000's | 2 (9.52) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
TSUKADA, Y | 2 |
de Valk, HW; Leenders, KL; Oudkerk, M; Reijngoud, DJ; Sijens, PE; van Spronsen, FJ | 1 |
Baker, GL; Blaskovics, ME; Filer, LJ; Koch, R; McDonnell, JE; Stegink, LD | 1 |
Baker, GL; Filer, LJ; McDonnell, JE; Stegink, LD | 2 |
Baert, AL; Breysem, L; François, B; Jaeken, J; Johannik, K; Marchal, G; Smet, MH; Van Hecke, P; Wilms, G | 1 |
Hájek, M; Hejcmanová, L; Prádný, J | 1 |
Apold, J; Bruland, O; Eiken, HG; Flatmark, T; Knappskog, PM; Martínez, A | 1 |
Hewson, AS; Knappskog, PM; Martinez, A; Parniak, MA; Scriver, CR; Treacy, EP; Waters, PI | 1 |
Bonafé, L; Burlina, AB; Burlina, AP; Ferrari, V; Suppiej, A; Zacchello, F | 1 |
Bhagavan, NV | 1 |
Koch, R | 1 |
Bell, EF; Filer, LJ; Krause, WL; Stegink, LD; Tephly, TR; Ziegler, EE | 1 |
Filer, LJ; Stegink, LD | 1 |
Bell, EF; Brummel, MC; Filer, LJ; Krause, WL; Stegink, LD; Wolf-Novak, LC; Ziegler, EE | 1 |
Galewicz, A; Gorska, D; Rodo, M; Zaremba, J | 1 |
Jenner, FA | 1 |
Barkin, E; Levy, HL | 1 |
2 trial(s) available for aspartic acid and BH4 Deficiency
Article | Year |
---|---|
Repeated ingestion of aspartame-sweetened beverages: further observations in individuals heterozygous for phenylketonuria.
Topics: Adult; Amino Acids; Aspartame; Aspartic Acid; Beverages; Female; Heterozygote; Humans; Male; Methanol; Phenylalanine; Phenylketonurias | 1990 |
Aspartame-sweetened beverage: effect on plasma amino acid concentrations in normal adults and adults heterozygous for phenylketonuria.
Topics: Adult; Amino Acids; Asparagine; Aspartame; Aspartic Acid; Beverages; Biological Transport; Dipeptides; Female; Glutamates; Glutamic Acid; Glutamine; Heterozygote; Humans; Kinetics; Male; Phenylalanine; Phenylketonurias; Tyrosine | 1987 |
19 other study(ies) available for aspartic acid and BH4 Deficiency
Article | Year |
---|---|
[AMINO ACID METABOLISM IN THE BRAIN AND BEHAVIORAL CHANGES].
Topics: Amino Acids; Aminobutyrates; Ammonia; Animals; Aspartic Acid; Behavior, Animal; Brain; Carbon Isotopes; Conditioning, Classical; Glutamates; Glutamine; Guinea Pigs; Phenylketonurias; Proteins; Rats; Reflex; Research | 1964 |
[BIOCHEMICAL STUDIES ON EXPERIMENTAL PHENYLKETONURIA].
Topics: Amino Acids; Animals; Aspartic Acid; Diet; Discrimination Learning; Glutamine; Haplorhini; Phenylalanine; Phenylketonurias; Pyruvates; Rabbits; Rats; Research; Tyrosine | 1964 |
1H MR chemical shift imaging detection of phenylalanine in patients suffering from phenylketonuria (PKU).
Topics: Adolescent; Adult; Aspartic Acid; Brain Chemistry; Cerebral Ventricles; Choline; Creatine; Female; Humans; Hydrogen; Image Processing, Computer-Assisted; Magnetic Resonance Spectroscopy; Male; Phenylalanine; Phenylketonurias | 2004 |
Plasma phenylalanine levels in phenylketonuric heterozygous and normal adults administered aspartame at 34 mg/kg body weight.
Topics: Adult; Aspartame; Aspartic Acid; Dipeptides; Female; Heterozygote; Humans; Male; Phenylalanine; Phenylketonurias; Sex Factors; Tyrosine | 1981 |
Effect of an abuse dose of aspartame upon plasma and erythrocyte levels of amino acids in phenylketonuric heterozygous and normal adults.
Topics: Amino Acids; Aspartame; Aspartic Acid; Dipeptides; Dose-Response Relationship, Drug; Erythrocytes; Female; Heterozygote; Humans; Kinetics; Male; Phenylalanine; Phenylketonurias | 1980 |
Localized brain proton NMR spectroscopy in young adult phenylketonuria patients.
Topics: Adolescent; Adult; Aspartic Acid; Brain Chemistry; Choline; Creatine; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Phenylketonurias | 1994 |
Proton in vivo spectroscopy of patients with hyperphenylalaninaemia.
Topics: Adult; Aspartic Acid; Biopterins; Brain; Brain Chemistry; Brain Diseases; Child; Choline; Creatine; Demyelinating Diseases; Female; Humans; Magnetic Resonance Imaging; Male; Phenylalanine; Phenylketonurias | 1993 |
PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systems.
Topics: Aspartic Acid; Cell Line; Cloning, Molecular; Escherichia coli; Exons; Genetic Variation; Glycine; Humans; Kidney; Kinetics; Mutagenesis, Site-Directed; Phenylalanine Hydroxylase; Phenylketonurias; Polymerase Chain Reaction; Recombinant Fusion Proteins | 1996 |
Comparative analysis of phenylalanine hydroxylase A104D mutant, associated with variant phenylketonuria, and wild-type enzyme.
Topics: Alanine; Aspartic Acid; Chromatography, Affinity; Chromatography, Gel; Humans; Kinetics; Phenylalanine Hydroxylase; Phenylketonurias; Point Mutation; Recombinant Fusion Proteins | 1997 |
Measurement of neurotransmitter metabolites in the cerebrospinal fluid of phenylketonuric patients under dietary treatment.
Topics: Adolescent; Adult; Aspartic Acid; Child; Dipeptides; Dopamine; Female; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Magnetic Resonance Imaging; Male; Phenylketonurias; Radiography; Serotonin | 2000 |
Effect of aspartame loading upon plasma and erythrocyte amino acid levels in phenylketonuric heterozygotes and normal adult subjects.
Topics: Adult; Amino Acids; Aspartame; Aspartic Acid; Dipeptides; Erythrocytes; Female; Heterozygote; Humans; Male; Phenylalanine; Phenylketonurias | 1979 |
Letter: Hazards in indiscriminate use of sweeteners containing phenylalanine.
Topics: Aspartic Acid; Diet; Dipeptides; Female; Fetus; Heterozygote; Homozygote; Humans; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Sweetening Agents | 1975 |
Letter: Safety of aspartame as a sweetener.
Topics: Aspartic Acid; Dipeptides; Female; Humans; Phenylalanine; Phenylketonurias; Pregnancy; Sweetening Agents | 1975 |
Synthetic sweetners: cyclamates, saccharin, aspartame.
Topics: Animals; Aspartame; Aspartic Acid; Beverages; Cyclamates; Cyclohexylamines; Diet, Reducing; Dipeptides; Female; Fetus; Food; Humans; Maternal-Fetal Exchange; Mice; Phenylketonurias; Piperazines; Placenta; Polyps; Pregnancy; Primates; Rats; Saccharin; United States; United States Food and Drug Administration; Urinary Bladder Neoplasms; Uterine Neoplasms | 1975 |
Aspartame metabolism in normal adults, phenylketonuric heterozygotes, and diabetic subjects.
Topics: Adult; Aspartame; Aspartic Acid; Blood Glucose; Diabetes Mellitus, Type 2; Dipeptides; Erythrocytes; Female; Glucagon; Heterozygote; Humans; Insulin; Lipids; Male; Methanol; Phenylalanine; Phenylketonurias; Reference Values | 1989 |
Aspartame. Review of safety issues. Council on Scientific Affairs.
Topics: Adolescent; Adult; Animals; Aspartame; Aspartic Acid; Brain Chemistry; Brain Diseases; Brain Neoplasms; Carbonated Beverages; Carcinogens; Child; Dietary Carbohydrates; Diketopiperazines; Dipeptides; Drug Stability; Endocrine System Diseases; Female; Glutamates; Glutamic Acid; Humans; Infant; Intellectual Disability; Methanol; Mice; Neurotransmitter Agents; Phenylalanine; Phenylketonurias; Piperazines; Pregnancy; Rats | 1985 |
A search for aspartylglycosaminuria in Poland.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Child, Institutionalized; Chromatography, Paper; Glycosuria; Humans; Intellectual Disability; Phenylketonurias; Poland | 1974 |
Medical research council unit for metabolic studies in psychiatry, Sheffield.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Bipolar Disorder; Catatonia; Circadian Rhythm; Cysteine; Humans; Intellectual Disability; Lithium; Mass Spectrometry; Mental Disorders; Metabolism, Inborn Errors; Periodicity; Phenylketonurias; Sleep; Vasopressins | 1973 |
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine | 1971 |