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2. Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations. Meire FM; Van Coster R; Cochaux P; Obermaier-Kusser B; Candaele C; Martin JJ Ophthalmic Genet; 1995 Sep; 16(3):119-26. PubMed ID: 8556281 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Harding AE; Sweeney MG; Miller DH; Mumford CJ; Kellar-Wood H; Menard D; McDonald WI; Compston DA Brain; 1992 Aug; 115 ( Pt 4)():979-89. PubMed ID: 1393514 [TBL] [Abstract][Full Text] [Related]
5. Leber's hereditary optic neuropathy with the 11 778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings. Jansen PH; van der Knaap MS; de Coo IF J Neurol Sci; 1996 Feb; 135(2):176-80. PubMed ID: 8867076 [TBL] [Abstract][Full Text] [Related]
7. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation. Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729 [TBL] [Abstract][Full Text] [Related]
8. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis. Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290 [TBL] [Abstract][Full Text] [Related]
9. Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis. Vanopdenbosch L; Dubois B; D'Hooghe MB; Meire F; Carton H J Neurol; 2000 Jul; 247(7):535-43. PubMed ID: 10993496 [TBL] [Abstract][Full Text] [Related]
10. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation. Lev D; Yanoov-Sharav M; Watemberg N; Leshinsky-Silver E; Lerman-Sagie T Eur J Paediatr Neurol; 2002; 6(2):121-3. PubMed ID: 11995959 [TBL] [Abstract][Full Text] [Related]
12. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations]. Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773 [TBL] [Abstract][Full Text] [Related]
13. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation. Shoffner JM; Brown MD; Stugard C; Jun AS; Pollock S; Haas RH; Kaufman A; Koontz D; Kim Y; Graham JR Ann Neurol; 1995 Aug; 38(2):163-9. PubMed ID: 7654063 [TBL] [Abstract][Full Text] [Related]
14. A case-control study of Leber's hereditary optic neuropathy. Charlmers RM; Harding AE Brain; 1996 Oct; 119 ( Pt 5)():1481-6. PubMed ID: 8931573 [TBL] [Abstract][Full Text] [Related]
15. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation. Olsen NK; Hansen AW; Nørby S; Edal AL; Jørgensen JR; Rosenberg T Acta Neurol Scand; 1995 May; 91(5):326-9. PubMed ID: 7639060 [TBL] [Abstract][Full Text] [Related]
16. HLA class II genotypes in Leber's hereditary optic neuropathy. Govan GG; Smith PR; Kellar-Wood H; Schapira AH; Harding AE J Neurol Sci; 1994 Nov; 126(2):193-6. PubMed ID: 7853025 [TBL] [Abstract][Full Text] [Related]
17. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population. Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587 [TBL] [Abstract][Full Text] [Related]
18. Wolff-Parkinson-White syndrome and isolated left ventricular abnormal trabeculation as a manifestation of Leber's hereditary optic neuropathy. Finsterer J; Stöllberger C; Kopsa W; Jaksch M Can J Cardiol; 2001 Apr; 17(4):464-6. PubMed ID: 11329546 [TBL] [Abstract][Full Text] [Related]
19. A multiple sclerosis-like illness in a man harboring the mtDNA 14484 mutation. Bhatti MT; Newman NJ J Neuroophthalmol; 1999 Mar; 19(1):28-33. PubMed ID: 10098545 [TBL] [Abstract][Full Text] [Related]