phenylalanine has been researched along with Ataxia with Lactic Acidosis in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brown, GK; Brown, RM; Clayton, PT; Head, RA; King, MD; Shahdadpuri, R; Zolkipli, Z | 1 |
| Brady, RO | 1 |
1 review(s) available for phenylalanine and Ataxia with Lactic Acidosis
| Article | Year |
|---|---|
Inherited metabolic diseases and pathogenesis of mental retardation.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Carbohydrate Metabolism, Inborn Errors; Cytochrome Reductases; Deoxyglucose; Dihydrolipoamide Dehydrogenase; Energy Metabolism; Gangliosides; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Phenylalanine; Pyruvate Dehydrogenase Complex Deficiency Disease | 1978 |
1 other study(ies) available for phenylalanine and Ataxia with Lactic Acidosis
| Article | Year |
|---|---|
Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency.
Topics: Autoantigens; Blotting, Western; Brain Chemistry; Child; Dihydrolipoyllysine-Residue Acetyltransferase; DNA Mutational Analysis; Fibroblasts; Globus Pallidus; Glutamic Acid; Humans; Leucine; Magnetic Resonance Imaging; Male; Mitochondrial Proteins; Mutation; Phenylalanine; Pyruvate Dehydrogenase Complex Deficiency Disease; Transfection | 2005 |