These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Hereditary optic neuropathies share a common mitochondrial coupling defect. Chevrollier A; Guillet V; Loiseau D; Gueguen N; de Crescenzo MA; Verny C; Ferre M; Dollfus H; Odent S; Milea D; Goizet C; Amati-Bonneau P; Procaccio V; Bonneau D; Reynier P Ann Neurol; 2008 Jun; 63(6):794-8. PubMed ID: 18496845 [TBL] [Abstract][Full Text] [Related]
7. Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve. Howell N Vision Res; 1997 Dec; 37(24):3495-507. PubMed ID: 9425526 [TBL] [Abstract][Full Text] [Related]
8. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Kellar-Wood H; Robertson N; Govan GG; Compston DA; Harding AE Ann Neurol; 1994 Jul; 36(1):109-12. PubMed ID: 8024249 [TBL] [Abstract][Full Text] [Related]
9. Mitochondrial DNA mutations in Leber's optic neuropathy. Hurko O Ann Neurol; 1994 May; 35(5):636. PubMed ID: 7910006 [No Abstract] [Full Text] [Related]
10. Update in molecular genetics: mitochondrial energy transduction disorders. Marzuki S; Sudoyo H; Lertrit P Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():155-61. PubMed ID: 8629096 [No Abstract] [Full Text] [Related]
11. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China]. Zhang LS; Huang Y; Li FY Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):349-51, 390. PubMed ID: 7994643 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial disorders in muscle. Schon EA Curr Opin Neurol Neurosurg; 1993 Feb; 6(1):19-26. PubMed ID: 8428062 [TBL] [Abstract][Full Text] [Related]
13. Oxidative stress and mitochondrial dysfunction in neurodegeneration. Tritschler HJ; Packer L; Medori R Biochem Mol Biol Int; 1994 Aug; 34(1):169-81. PubMed ID: 7849618 [TBL] [Abstract][Full Text] [Related]
14. Mitochondria take center stage in aging and neurodegeneration. Beal MF Ann Neurol; 2005 Oct; 58(4):495-505. PubMed ID: 16178023 [TBL] [Abstract][Full Text] [Related]
15. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON. Rödel G; Laubhan R; Scheuerle A; Skowronek P; Haferkamp O Eur J Med Res; 1996 Jul; 1(10):491-4. PubMed ID: 9438147 [TBL] [Abstract][Full Text] [Related]
16. OPA1 mutations and mitochondrial DNA damage: keeping the magic circle in shape. Zeviani M Brain; 2008 Feb; 131(Pt 2):314-7. PubMed ID: 18222990 [No Abstract] [Full Text] [Related]
17. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy]. Wang Y; Tong Y; Hu SX; Wang JY; Shao JB; Zhang HX Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):397-400. PubMed ID: 17680528 [TBL] [Abstract][Full Text] [Related]
18. Aging genes and diseases of the aging nervous system. Conneally PM Adv Neurol; 1991; 56():233-6. PubMed ID: 1830187 [No Abstract] [Full Text] [Related]
19. Pathogenicity of homoplasmic mitochondrial DNA mutation and nuclear gene involvement. Odawara M; Maki H; Yamada N J Med Genet; 1999 Dec; 36(12):934-5. PubMed ID: 10636741 [No Abstract] [Full Text] [Related]