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27. A SEX-LINKED HEREDO-DEGENERATIVE NEUROLOGICAL DISORDER, ASSOCIATED WITH LEBER'S OPTIC ATROPHY. II. LABORATORY INVESTIGATIONS. WENT LN J Neurol Sci; 1964; 1(1):81-7. PubMed ID: 14174046 [No Abstract] [Full Text] [Related]
28. 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]
29. Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36. Keen TJ; Mohamed MD; McKibbin M; Rashid Y; Jafri H; Maumenee IH; Inglehearn CF Eur J Hum Genet; 2003 May; 11(5):420-3. PubMed ID: 12734549 [TBL] [Abstract][Full Text] [Related]
30. Novel use of idebenone in Leber's hereditary optic neuropathy in Hong Kong. Cheng SW; Ko CH; Yau SK; Mak C; Yuen YF; Lee CY Hong Kong Med J; 2014 Oct; 20(5):451-4. PubMed ID: 25307075 [TBL] [Abstract][Full Text] [Related]
32. [Leber's hereditary optic neuropathy--two case reports]. Mulak M; Kisza K; Dembska K; Misiuk-Hojło M Klin Oczna; 2013; 115(3):238-41. PubMed ID: 24741932 [TBL] [Abstract][Full Text] [Related]
33. Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2). Porto FB; Perrault I; Hicks D; Rozet JM; Hanoteau N; Hanein S; Kaplan J; Sahel JA Adv Exp Med Biol; 2003; 533():59-68. PubMed ID: 15180248 [No Abstract] [Full Text] [Related]
34. [Contribution to the pathogenesis of Leber's disease; Role of the vascular factor]. MASSION-VERNIORY L; POTVIN AM Rev Neurol (Paris); 1946; 78():91-102. PubMed ID: 20994601 [No Abstract] [Full Text] [Related]
35. Leber's hereditary optic atrophy in a Canadian family. BIRD A; McEACHERN D Can Med Assoc J; 1949 Oct; 61(4):376-83. PubMed ID: 18140583 [No Abstract] [Full Text] [Related]
36. Bilateral vision loss due to Leber's hereditary optic neuropathy after long-term alcohol, nicotine and drug abuse. Maass J; Matthé E Doc Ophthalmol; 2018 Apr; 136(2):145-153. PubMed ID: 29372350 [TBL] [Abstract][Full Text] [Related]
37. Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis. Kim JY; Hwang JM; Park SS Ann Neurol; 2002 May; 51(5):630-4. PubMed ID: 12112111 [TBL] [Abstract][Full Text] [Related]