n-acetylaspartic acid has been researched along with Metabolism, Inborn Errors in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Berry, GT; Jan, W; Kaplan, PB; Kaye, EM; Wang, ZJ; Zimmerman, RA | 1 |
| Amorini, AM; Bellia, F; Ceccarelli, L; Di Pietro, V; Donzelli, S; Francis, JS; Giardina, B; Janson, CG; Lazzarino, G; Leone, P; Tavazzi, B | 1 |
| Bruhn, H; Frahm, J; Hanefeld, F; Kruse, B | 1 |
| Ernst, S; Heindel, W; Kugel, H; Lackner, K; Roth, B | 1 |
| Divry, P; Mathieu, M | 1 |
5 other study(ies) available for n-acetylaspartic acid and Metabolism, Inborn Errors
| Article | Year |
|---|---|
MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.
Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Amino Acids, Branched-Chain; Aspartic Acid; Basal Ganglia; Biomarkers; Brain Stem; Cerebellum; Cerebral Cortex; Creatine; Diffusion Magnetic Resonance Imaging; Female; Follow-Up Studies; Humans; Infant; Infant Welfare; Infant, Newborn; Ketone Oxidoreductases; Lactic Acid; Magnetic Resonance Spectroscopy; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Multienzyme Complexes; Phosphocreatine; Radiography; Statistics as Topic; Time Factors | 2003 |
Simultaneous high performance liquid chromatographic separation of purines, pyrimidines, N-acetylated amino acids, and dicarboxylic acids for the chemical diagnosis of inborn errors of metabolism.
Topics: Adolescent; Adult; Amino Acids; Amniotic Fluid; Aspartic Acid; Canavan Disease; Child; Child, Preschool; Chromatography, High Pressure Liquid; Dicarboxylic Acids; Humans; Infant; Mass Screening; Metabolism, Inborn Errors; Middle Aged; Prenatal Diagnosis; Purines; Pyrimidines; Reproducibility of Results; Sensitivity and Specificity; Spectrophotometry, Ultraviolet | 2005 |
In vivo proton magnetic resonance spectroscopy of the brain in a patient with L-2-hydroxyglutaric acidemia.
Topics: Adolescent; Aspartic Acid; Biomarkers; Brain; Female; Glutarates; Humans; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Metabolism, Inborn Errors; Nerve Degeneration | 1994 |
Proton MR spectroscopy in infants with cerebral energy deficiency due to hypoxia and metabolic disorders.
Topics: Aspartic Acid; Basal Ganglia; Brain; Brain Diseases, Metabolic; Child, Preschool; Follow-Up Studies; Humans; Hypoxia; Infant; Lactic Acid; Magnetic Resonance Imaging; Metabolism, Inborn Errors; Methylamines; Oxidative Phosphorylation; Protons; Severity of Illness Index | 1998 |
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease.
Topics: Amidohydrolases; Aspartic Acid; Central Nervous System Diseases; Genes, Recessive; Humans; Metabolism, Inborn Errors; Nerve Degeneration | 1989 |