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.
96 related articles for article (PubMed ID: 1880538)
21. [Extrapyramidal rigidity with dystonia, optic atrophy and bilateral putaminal lesions in an adolescent. Juvenile form of Leigh's disease (author's transl)]. Rondot P; de Recondo J; Davous P; Fredy D; Roux FX Rev Neurol (Paris); 1982; 138(2):143-8. PubMed ID: 7100740 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. [Leber's hereditary optic neuropathy with onset at the age of 54 years]. Nakamura N; Furukawa Y; Fujiki K; Hayakawa M; Mizuno Y Rinsho Shinkeigaku; 1994 Mar; 34(3):258-60. PubMed ID: 8200145 [TBL] [Abstract][Full Text] [Related]
24. Optic nerve enhancement on orbital magnetic resonance imaging in Leber's hereditary optic neuropathy. Vaphiades MS; Newman NJ J Neuroophthalmol; 1999 Dec; 19(4):238-9. PubMed ID: 10608675 [TBL] [Abstract][Full Text] [Related]
25. Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family. Cortelli P; Montagna P; Avoni P; Sangiorgi S; Bresolin N; Moggio M; Zaniol P; Mantovani V; Barboni P; Barbiroli B Neurology; 1991 Aug; 41(8):1211-5. PubMed ID: 1866007 [TBL] [Abstract][Full Text] [Related]
26. Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. Holt IJ; Miller DH; Harding AE J Med Genet; 1989 Dec; 26(12):739-43. PubMed ID: 2575667 [TBL] [Abstract][Full Text] [Related]
27. In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by 31P magnetic resonance spectroscopy. Lodi R; Taylor DJ; Tabrizi SJ; Kumar S; Sweeney M; Wood NW; Styles P; Radda GK; Schapira AH Ann Neurol; 1997 Oct; 42(4):573-9. PubMed ID: 9382468 [TBL] [Abstract][Full Text] [Related]
28. Nonfamilial and unusual cases of Leber's hereditary optic neuropathy identified by mitochondrial DNA analysis. Isashiki Y; Ohba N; Uto M; Nakagawa M; Nakano T; Kitahara K; Hotta A; Okamura R; Ozaki M; Futami Y Jpn J Ophthalmol; 1992; 36(2):197-204. PubMed ID: 1513067 [TBL] [Abstract][Full Text] [Related]
30. Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team. Newman NJ; Torroni A; Brown MD; Lott MT; Fernandez MM; Wallace DC Am J Ophthalmol; 1994 Aug; 118(2):158-68. PubMed ID: 8053461 [TBL] [Abstract][Full Text] [Related]
31. Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathy. Borruat FX; Green WT; Graham EM; Sweeney MG; Morgan-Hughes JA; Sanders MD Br J Ophthalmol; 1992 Sep; 76(9):571-3. PubMed ID: 1420066 [TBL] [Abstract][Full Text] [Related]
32. Acquired mitochondrial impairment as a cause of optic nerve disease. Sadun A Trans Am Ophthalmol Soc; 1998; 96():881-923. PubMed ID: 10360310 [TBL] [Abstract][Full Text] [Related]
33. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy. Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798 [TBL] [Abstract][Full Text] [Related]