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34. A Case of Atypical Leber Hereditary Optic Neuropathy With Slow, Symmetrical Progression Over Three Years. Chun BY; Kim DW; Son BJ J Neuroophthalmol; 2018 Sep; 38(3):421-422. PubMed ID: 30106804 [No Abstract] [Full Text] [Related]
35. [Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy]. Carrasco Salas P; Palma Milla C; López Montiel J; Benito C; Franco Freire S; López Siles J Med Clin (Barc); 2016 Feb; 146(4):163-6. PubMed ID: 26683077 [TBL] [Abstract][Full Text] [Related]
36. Clinical variability in maternally inherited leber hereditary optic neuropathy with the G14459A mutation. Tarnopolsky MA; Baker SK; Myint T; Maxner CE; Robitaille J; Robinson BH Am J Med Genet A; 2004 Feb; 124A(4):372-6. PubMed ID: 14735584 [TBL] [Abstract][Full Text] [Related]
37. Leber's hereditary optic neuropathy masquerading as optic neuritis with spontaneous visual recovery. Hsu TK; Wang AG; Yen MY; Liu JH Clin Exp Optom; 2014 Jan; 97(1):84-6. PubMed ID: 23905692 [TBL] [Abstract][Full Text] [Related]
38. [Leber's optic neuropathy: a mitochondrial disease revealing its secret]. Nikoskelainen E; Savontaus ML Duodecim; 1998; 114(3):303-6. PubMed ID: 10895506 [No Abstract] [Full Text] [Related]
39. Parkinsonism in a patient with Leber hereditary optic neuropathy (LHON). Vital C; Julien J; Martin-Negrier ML; Lagueny A; Ferrer X; Vital A Rev Neurol (Paris); 2015 Sep; 171(8-9):679-80. PubMed ID: 25917160 [No Abstract] [Full Text] [Related]
40. 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] [Previous] [Next] [New Search]