aspartic acid has been researched along with Genetic Diseases, X-Chromosome Linked in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Duman, F; Emre, S; Konus, I; Ozsoy, E; Turkcuoglu, P | 1 |
| Barberini, L; Cherchi, MV; Cocco, E; Corongiu, D; Mallarini, G; Marrosu, G; Marrosu, MG; Mura, M; Murru, MR; Tranquilli, S; Vannelli, A | 1 |
2 other study(ies) available for aspartic acid and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Evaluation of Metabolite Changes in the Occipital Cortex of Patients with Idiopathic Infantile Nystagmus or Bilateral Ametropic Amblyopia by Magnetic Resonance Spectroscopy.
Topics: Adolescent; Amblyopia; Aspartic Acid; Biomarkers; Child; Child, Preschool; Choline; Creatine; Female; Follow-Up Studies; Genetic Diseases, X-Linked; Humans; Magnetic Resonance Spectroscopy; Male; Nystagmus, Congenital; Occipital Lobe; Prospective Studies | 2019 |
A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities.
Topics: Adolescent; Adult; Aspartic Acid; Brain Chemistry; Brain Stem; Charcot-Marie-Tooth Disease; Connexins; Creatinine; DNA Mutational Analysis; Evoked Potentials; Female; Gap Junction beta-1 Protein; Genetic Diseases, X-Linked; Genetic Predisposition to Disease; Genetic Testing; Humans; Lateral Ventricles; Linkage Disequilibrium; Magnetic Resonance Spectroscopy; Mutation, Missense; Nerve Fibers, Myelinated; Neural Conduction; Neural Pathways; Pedigree; Telencephalon | 2006 |