glutamic acid has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abulseoud, O; Gropman, AL; Harris, KC; Ross, BD; Sailasuta, N | 1 |
| Bonnefont, JP; Calvas, P; Gilbert-Dussardier, B; Munnich, A; Rabier, D; Saudubray, JM; Ségues, B; Veber, PS | 1 |
| Bale, AE; Desnick, RJ; Fox, JE; Sansaricq, C; Topaloglu, AK; Tuchman, M | 1 |
3 other study(ies) available for glutamic acid and Deficiency Disease, Ornithine Carbamoyltransferase
| Article | Year |
|---|---|
Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.
Topics: Adult; Brain; Carbon Isotopes; Case-Control Studies; Female; Glucose; Glutamic Acid; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Ornithine Carbamoyltransferase Deficiency Disease | 2009 |
A 3-base pair in-frame deletion in exon 8 (delGlu272/273) of the ornithine transcarbamylase gene in late-onset hyperammonemic coma.
Topics: Adolescent; Age of Onset; Ammonia; Coma; Exons; Female; Glutamic Acid; Humans; Male; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Pedigree; Polymerase Chain Reaction; Reading Frames; Sequence Deletion | 1996 |
Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G.
Topics: Female; Glutamic Acid; Glycine; Humans; Infant; Male; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Point Mutation; Pregnancy; Prenatal Diagnosis | 1999 |