nad has been researched along with Optic Atrophy, Hereditary, Leber 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 | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cerná, L; Hansíková, H; Houst'ková, H; Houstek, J; Kaplanová, V; Misovicová, N; Zeman, J | 1 |
Achilli, A; Barbiroli, B; Barboni, P; Baruzzi, A; Bucchi, L; Carelli, V; Dotti, M; Federico, A; Ghelli, A; Lodi, R; Lugaresi, A; Rengo, C; Torroni, A; Valentino, ML | 1 |
2 other study(ies) available for nad and Optic Atrophy, Hereditary, Leber
Article | Year |
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Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.
Topics: Alanine; Analysis of Variance; DNA Mutational Analysis; DNA, Mitochondrial; Family Health; Female; Glycine; Humans; Longitudinal Studies; Male; NAD; Optic Atrophy, Hereditary, Leber; Oxidoreductases; Pedigree; Point Mutation; Rotenone | 2004 |
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.
Topics: Adult; Aged; DNA Mutational Analysis; DNA, Mitochondrial; Family Health; Female; Ferricyanides; Glutamic Acid; Haplotypes; Humans; Inhibitory Concentration 50; Lysine; Magnetic Resonance Spectroscopy; Male; Microscopy, Electron, Transmission; Middle Aged; Mitochondria, Muscle; Models, Molecular; Muscle, Skeletal; Mutation; NAD; NADH Dehydrogenase; Occipital Lobe; Optic Atrophy, Hereditary, Leber; Pedigree; Polymorphism, Restriction Fragment Length; Radionuclide Imaging; Rotenone; Sequence Analysis, Protein; Succinate Dehydrogenase; Visual Acuity; Visual Fields | 2004 |