glutamic acid has been researched along with Metabolism, Inborn Errors in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bahi-Buisson, N; Dulac, O; Fallet-Bianco, C; Galmiche-Rolland, L; Gataullina, S; Kaminska, A; Lauer-Zillhardt, J; Ottolenghi, C; Pontoizeau, C | 1 |
| Gibson, KM; Gupta, M; Jakobs, C; Pearl, PL; Smit, LM; Snead, OC; Tuchman, M; Vezina, LG | 1 |
| Gibson, KM; Jakobs, C; Struys, EA | 1 |
| Doi, H; Itoh, K; Ozand, PT; Sakuraba, H; Shimmoto, M; Takiguchi, K | 1 |
| de Kremer, RD; Larovere, L; Latini, A | 1 |
5 other study(ies) available for glutamic acid and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Epileptic Phenotype of Two Siblings with Asparagine Synthesis Deficiency Mimics Neonatal Pyridoxine-Dependent Epilepsy.
Topics: Aspartate-Ammonia Ligase; Brain Diseases; Child, Preschool; Diagnosis; Epilepsy; Female; Glutamic Acid; Humans; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Siblings | 2016 |
Significant behavioral disturbances in succinic semialdehyde dehydrogenase (SSADH) deficiency (gamma-hydroxybutyric aciduria).
Topics: Adult; Aldehyde Oxidoreductases; Atrophy; Cerebellum; Chromatography, High Pressure Liquid; Chromatography, Ion Exchange; Female; gamma-Aminobutyric Acid; Globus Pallidus; Glutamic Acid; Hallucinations; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Intellectual Disability; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Sodium Oxybate; Statistics as Topic; Succinate-Semialdehyde Dehydrogenase | 2003 |
Novel insights into L-2-hydroxyglutaric aciduria: mass isotopomer studies reveal 2-oxoglutaric acid as the metabolic precursor of L-2-hydroxyglutaric acid.
Topics: Alcohol Oxidoreductases; Carbon Isotopes; Cell Line; Citric Acid; Deuterium; Gas Chromatography-Mass Spectrometry; Glucose; Glutamic Acid; Glutarates; Humans; Ketoglutaric Acids; Lymphocytes; Metabolism, Inborn Errors; Oxidation-Reduction | 2007 |
Structural and functional study of K453E mutant protective protein/cathepsin A causing the late infantile form of galactosialidosis.
Topics: Amino Acid Substitution; beta-Galactosidase; Blotting, Northern; Carboxypeptidases; Cathepsin A; Child; Crystallography, X-Ray; Female; Glutamic Acid; Humans; Immunohistochemistry; Lysine; Metabolism, Inborn Errors; Models, Molecular; Mutation, Missense; Neuraminidase; Protein Structure, Quaternary; White People | 2000 |
Purines, lactate and myo-inositol in CSF might reflect excitotoxicity in inherited metabolic disorders.
Topics: Child; Child, Preschool; Glutamic Acid; Humans; Hypoxanthine; Infant; Inositol; Lactates; Metabolism, Inborn Errors; Purines; Receptors, Glutamate; Uric Acid; Uridine; Xanthine | 2000 |