nad has been researched along with Hereditary Optic Atrophy in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Robinson, BH | 1 |
| Cock, HR; Cooper, JM; Schapira, AH | 1 |
2 other study(ies) available for nad and Hereditary Optic Atrophy
| Article | Year |
|---|---|
Use of fibroblast and lymphoblast cultures for detection of respiratory chain defects.
Topics: Animals; Cells, Cultured; Culture Media; Culture Techniques; DNA, Mitochondrial; Fibroblasts; Galactose; Genetic Diseases, Inborn; Glycolysis; Humans; Kinetics; Lactates; Lymphocytes; Mitochondria; Models, Biological; NAD; Optic Atrophies, Hereditary; Oxidation-Reduction; Oxidative Phosphorylation; Pyruvates; Skin | 1996 |
Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
Topics: Adenosine Triphosphate; Adult; DNA, Mitochondrial; Electron Transport; Electron Transport Complex I; Fibroblasts; Humans; Middle Aged; Mitochondria, Muscle; Mutation; NAD; NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Reverse Transcriptase Polymerase Chain Reaction; Rotenone; Uncoupling Agents | 1999 |