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23. Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification. Hotta Y; Hayakawa M; Saito K; Kanai A; Nakajima A; Fujiki K Am J Ophthalmol; 1989 Nov; 108(5):601-2. PubMed ID: 2817063 [No Abstract] [Full Text] [Related]
24. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy. Yen MY; Wei YH; Liu JH J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169 [TBL] [Abstract][Full Text] [Related]
25. Evidence for a metabolic trigger for Leber's hereditary optic neuropathy. A case report. DuBois LG; Feldon SE J Clin Neuroophthalmol; 1992 Mar; 12(1):15-6. PubMed ID: 1532594 [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. [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]
28. Leber's hereditary optic neuropathy--case report and literature review. Teive HA; Troiano AR; Raskin S; Werneck LC Sao Paulo Med J; 2004 Nov; 122(6):276-9. PubMed ID: 15692724 [TBL] [Abstract][Full Text] [Related]
29. Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy. Isashiki Y; Nakagawa M Jpn J Ophthalmol; 1991; 35(3):259-67. PubMed ID: 1770665 [TBL] [Abstract][Full Text] [Related]
30. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy]. Toyo-Oka Y; Wada C; Yamabe H; Inoue M; Ishigaki M; Matsuyama N; Ohnuki Y; Ichibe Y; Wakakura M; Ohtani H Rinsho Byori; 1996 Jul; 44(7):676-80. PubMed ID: 8741498 [TBL] [Abstract][Full Text] [Related]
31. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation. Yamada K; Mashima Y; Kigasawa K; Miyashita K; Wakakura M; Oguchi Y J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781 [TBL] [Abstract][Full Text] [Related]
33. 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]
37. Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy. Ortiz RG; Newman NJ; Manoukian SV; Diesenhouse MC; Lott MT; Wallace DC Am J Ophthalmol; 1992 May; 113(5):561-6. PubMed ID: 1575231 [TBL] [Abstract][Full Text] [Related]
38. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene. Leo-Kottler B; Christ-Adler M; Baumann B; Zrenner E; Wissinger B Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108 [TBL] [Abstract][Full Text] [Related]
39. Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation. Oostra RJ; Bolhuis PA; Zorn-Ende I; de Kok-Nazaruk MM; Bleeker-Wagemakers EM Hum Genet; 1994 Sep; 94(3):265-70. PubMed ID: 8076942 [TBL] [Abstract][Full Text] [Related]