Page last updated: 2024-08-17

nad and Optic Atrophy, Hereditary, Leber

nad has been researched along with Optic Atrophy, Hereditary, Leber in 2 studies

Research

Studies (2)

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

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

Other Studies

2 other study(ies) available for nad and Optic Atrophy, Hereditary, Leber

Article	Year
Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family. Journal of the neurological sciences, 2004, Aug-30, Volume: 223, Issue:2 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. Annals of neurology, 2004, Volume: 56, Issue:5 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

Article

Year

Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.

Journal of the neurological sciences, 2004, Aug-30, Volume: 223, Issue:2

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.

Annals of neurology, 2004, Volume: 56, Issue:5

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