Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Sclerosis and LHON[original query] |
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[Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations]. Revue neurologique 2001 May 157 (5): 537-41. Pénisson-Besnier I, Moreau C, Jacques C, Roger J C, Dubas F, Reynier |
Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathy. Chinese medical journal 2002 1 113 (8): 743-6. Feng X, Pu W, Gao D, Isashiki Y, Ohba |
Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran. European neurology 2004 51 (2): 68-71. Houshmand M, Sanati M-H, Rashedi I, Sharifpanah F, Asghari E, Lotfi |
Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis. European journal of neurology : the official journal of the European Federation of Neurological Societies 2007 Jan 14 (1): 44-7. Mihailova S M, Ivanova M I, Quin L M, Naumova E |
Mitochondrial mutation in Iranian patients with multiple sclerosis, correlation between haplogroups H, A and clinical manifestations. Cellular and molecular neurobiology 2009 May 29 (3): 341-6. Ghabaee Mojdeh, Omranisikaroudi Motahar, Amrisaroukolaei Shahla, Meysamie Alipasha, Sahraian Mohammad Ali, Bayati Asghar, Sanati Mohammad Hossein, Houshman Mossoud, Sadeghian Homa, Vajihazaman Khali |
Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination. Neurology 2011 Mar 76 (9): 774-80. Venkateswaran S, Zheng K, Sacchetti M, Gagne D, Arnold D L, Sadovnick A D, Scherer S W, Banwell B, Bar-Or A, Simon D K, |
No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis. Mitochondrion 2017 Aug . Andalib Sasan, Talebi Mahnaz, Sakhinia Ebrahim, Farhoudi Mehdi, Sadeghi-Bazargani Homayoun, Masoudian Nooshin, Vafaee Manouchehr Seyedi, Gjedde Albe |
Analysis of the entire mitochondrial genome reveals Leber's hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis. Scientific reports 2022 Jun 12 (1): 11099. Al-Kafaji Ghada, Alharbi Maram A, Alkandari Hasan, Salem Abdel Halim, Bakhiet Mo |
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- Page last updated:Apr 22, 2024
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