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24. Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients. Jiang Z; Yu J; Xia B; Zhuo G Mitochondrial DNA A DNA Mapp Seq Anal; 2016; 27(2):1564-6. PubMed ID: 25186221 [TBL] [Abstract][Full Text] [Related]
25. Mitochondrial abnormalities in patients with LHON-like optic neuropathies. Abu-Amero KK; Bosley TM Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4211-20. PubMed ID: 17003408 [TBL] [Abstract][Full Text] [Related]
26. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy. Nakamura M Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918 [TBL] [Abstract][Full Text] [Related]
27. Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy. Scolding NJ; Kellar-Wood HF; Shaw C; Shneerson JM; Antoun N Ann Neurol; 1996 Mar; 39(3):352-60. PubMed ID: 8602754 [TBL] [Abstract][Full Text] [Related]
28. Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome). Rötig A; Cormier V; Chatelain P; Francois R; Saudubray JM; Rustin P; Munnich A J Inherit Metab Dis; 1993; 16(3):527-30. PubMed ID: 7609443 [No Abstract] [Full Text] [Related]
29. Presentation and clinical course of Wolfram (DIDMOAD) syndrome from North India. Ganie MA; Laway BA; Nisar S; Wani MM; Khurana ML; Ahmad F; Ahmed S; Gupta P; Ali I; Shabir I; Shadan A; Ahmed A; Tufail S Diabet Med; 2011 Nov; 28(11):1337-42. PubMed ID: 21726277 [TBL] [Abstract][Full Text] [Related]
30. Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis. Mihailova SM; Ivanova MI; Quin LM; Naumova EJ Eur J Neurol; 2007 Jan; 14(1):44-7. PubMed ID: 17222112 [TBL] [Abstract][Full Text] [Related]
31. Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran. Houshmand M; Sanati MH; Rashedi I; Sharifpanah F; Asghari E; Lotfi J Eur Neurol; 2004; 51(2):68-71. PubMed ID: 14671420 [TBL] [Abstract][Full Text] [Related]
32. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood]. Yang JH; Tong Y; Li BH; Chen YK Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367 [TBL] [Abstract][Full Text] [Related]
33. [From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)]. Pennings RJ; Dikkeschei LD; Cremers CW; van den Ouweland JM Ned Tijdschr Geneeskd; 2002 May; 146(21):985-7. PubMed ID: 12058630 [TBL] [Abstract][Full Text] [Related]
34. Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy. Gómez-Durán A; Pacheu-Grau D; Martínez-Romero I; López-Gallardo E; López-Pérez MJ; Montoya J; Ruiz-Pesini E Biochim Biophys Acta; 2012 Aug; 1822(8):1216-22. PubMed ID: 22561905 [TBL] [Abstract][Full Text] [Related]
35. Mitochondrial DNA mutations in diseases of energy metabolism. Wallace DC J Bioenerg Biomembr; 1994 Jun; 26(3):241-50. PubMed ID: 8077179 [TBL] [Abstract][Full Text] [Related]
36. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Strom TM; Hörtnagel K; Hofmann S; Gekeler F; Scharfe C; Rabl W; Gerbitz KD; Meitinger T Hum Mol Genet; 1998 Dec; 7(13):2021-8. PubMed ID: 9817917 [TBL] [Abstract][Full Text] [Related]
37. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy]. Feng X; Pu W; Gao D Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415 [TBL] [Abstract][Full Text] [Related]
38. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans. Kim JY; Hwang JM; Chang BL; Park SS J Neurol; 2003 Mar; 250(3):278-81. PubMed ID: 12638016 [TBL] [Abstract][Full Text] [Related]