pyrrolidonecarboxylic acid has been researched along with Nervous System Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Prusiner, SB | 1 |
| Jellum, E; Marstein, S; Nesbakken, R; Perry, TL | 1 |
| Board, P; Carlsson, B; Dahl, N; Gali, R; Larsson, A; Mannervik, B; Pigg, M; Ristoff, E | 1 |
| Beutler, E | 1 |
1 review(s) available for pyrrolidonecarboxylic acid and Nervous System Diseases
| Article | Year |
|---|---|
Disorders of glutamate metabolism and neurological dysfunction.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; gamma-Aminobutyric Acid; Glutamates; Glutamine; Glutathione; Histidine; Humans; Ketoglutaric Acids; Nervous System Diseases; Proline; Pyrrolidonecarboxylic Acid | 1981 |
3 other study(ies) available for pyrrolidonecarboxylic acid and Nervous System Diseases
| Article | Year |
|---|---|
Biochemical investigations of biopsied brain tissue and autopsied organs from a patient with pyroglutamic acidemia (5-oxoprolinemia).
Topics: Adult; Amino Acids; Brain; Glutathione; Glutathione Synthase; Humans; Male; Nervous System Diseases; Pyrrolidinones; Pyrrolidonecarboxylic Acid | 1981 |
Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunction.
Topics: Acidosis; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Anemia, Hemolytic; Animals; Blotting, Southern; Child, Preschool; Glutathione Synthase; Humans; Infant, Newborn; Molecular Sequence Data; Mutation; Nervous System Diseases; Phenotype; Point Mutation; Polymerase Chain Reaction; Pyrrolidonecarboxylic Acid; Rats; Recombinant Proteins; Restriction Mapping; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Xenopus | 1997 |
Editorial: Glutathione deficiency, pyroglutamic acidemia and amino acid transport.
Topics: Amino Acids; Anemia, Hemolytic, Congenital Nonspherocytic; Biological Transport, Active; Erythrocytes; gamma-Glutamyltransferase; Glutathione; Humans; Nervous System Diseases; Peptide Synthases; Pyroglutamate Hydrolase; Pyrrolidinones; Pyrrolidonecarboxylic Acid | 1976 |