aspartic acid has been researched along with Ataxias, Hereditary in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (50.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baracca, A; Casalena, GA; DiMauro, S; Lenaz, G; Sgarbi, G; Solaini, G | 1 |
| Cai, Y; Gao, Y; Guo, X; Li, D; Liang, Y; Lim, CC; Ma, L; Yin, H | 1 |
| Blaschek, A; Ebinger, F; Goebel, HH; Harting, I; Haupt, M; Rating, D; Sartor, K; Seitz, A; Wolf, NI | 1 |
| Kanazawa, I | 1 |
| Kish, SJ; Mastrogiacomo, F | 1 |
| Bartolozzi, C; Bianchi, MC; Frontali, M; Mascalchi, M; Plasmati, R; Salvi, F; Tassinari, CA; Tessa, C; Tosetti, M; Valzania, F | 1 |
1 review(s) available for aspartic acid and Ataxias, Hereditary
| Article | Year |
|---|---|
[Neurochemical aspects of spinocerebellar degeneration].
Topics: Aspartic Acid; Cerebellum; gamma-Aminobutyric Acid; Glutamates; Homocysteine; Humans; Neurotransmitter Agents; Spinocerebellar Degenerations | 1993 |
1 trial(s) available for aspartic acid and Ataxias, Hereditary
| Article | Year |
|---|---|
Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1.
Topics: Adult; Aspartic Acid; Brain Chemistry; Cerebellum; Choline; Chromosome Mapping; Creatine; DNA; Female; Genetic Linkage; Heterozygote; Humans; Inositol; Italy; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Neurologic Examination; Pedigree; Pons; Spinocerebellar Degenerations; Statistics, Nonparametric | 1998 |
4 other study(ies) available for aspartic acid and Ataxias, Hereditary
| Article | Year |
|---|---|
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy.
Topics: Adenosine Triphosphate; Anti-Infective Agents, Local; Aspartic Acid; C-Reactive Protein; Cell Line; Cell Survival; DNA, Mitochondrial; Energy Metabolism; Gramicidin; Humans; Ketoglutaric Acids; Leigh Disease; Mitochondria; Mitochondrial Proton-Translocating ATPases; Mutation; Nerve Tissue Proteins; Oligomycins; Oxidative Phosphorylation; Retinitis Pigmentosa; Spinocerebellar Degenerations | 2009 |
Combined MR spectroscopic imaging and diffusion tensor MRI visualizes corticospinal tract degeneration in amyotrophic lateral sclerosis.
Topics: Adult; Amyotrophic Lateral Sclerosis; Aspartic Acid; Brain Mapping; Case-Control Studies; Creatine; Diffusion Magnetic Resonance Imaging; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Pyramidal Tracts; Spinocerebellar Degenerations | 2004 |
T2-hyperintense cerebellar cortex in Marinesco-Sjögren syndrome.
Topics: Aspartic Acid; Cerebellar Cortex; Cerebral Cortex; Child; Child, Preschool; Consanguinity; Diagnosis, Differential; Female; Humans; Infant; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Neuroaxonal Dystrophies; Spinocerebellar Degenerations | 2004 |
Cerebellar alpha-ketoglutarate dehydrogenase activity is reduced in spinocerebellar ataxia type 1.
Topics: Adult; Aspartic Acid; Cerebellum; Cerebral Cortex; Energy Metabolism; Glutamates; Glutamic Acid; Humans; Ketoglutarate Dehydrogenase Complex; Neurotransmitter Agents; Reference Values; Spinocerebellar Degenerations | 1994 |