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Records 1-17

Query Trace: Mitochondrial Diseases and ND6[orginal query]

Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms. Acta ophthalmologica 2015 Oct . Widgren Paula, Hurme Anri, Falck Aura, Keski-Filppula Riikka, Remes Anne M, Moilanen Jukka, Majamaa Kari, Kervinen Marko, Uusimaa Johan Similar articles in PubMed
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families. Mitochondrion 2013 Nov 13 (6): 772-81. Zhang Juanjuan, Zhao Fuxin, Fu Qun, Liang Min, Tong Yi, Liu Xiaoling, Lin Bei, Mi Hui, Zhang Minglian, Wei Qi-Ping, Xue Ling, Jiang Pingping, Zhou Xiangtian, Mo Jun Qin, Huang Taosheng, Qu Jia, Guan Min-X Similar articles in PubMed
Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia. Acta ophthalmologica 2013 Nov 91 (7): 630-4. Korkiamäki Paula, Kervinen Marko, Karjalainen Karoliina, Majamaa Kari, Uusimaa Johanna, Remes Anne Similar articles in PubMed
Applications of the method of high resolution melting analysis for diagnosis of Leber's disease and the three primary mutation spectrum of LHON in the Han Chinese population. Gene 2013 Jan 512 (1): 108-12. Cui Guanglin, Ding Hu, Xu Yujun, Li Bin, Wang Dao W Similar articles in PubMed
[A clinical study of Leber hereditary optic neuropathy]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2012 Dec 48 (12): 1065-8. Wei Qi-Ping, Sun Yan-Hong, Zhou Xiang-tian, Zhou Jian, Gong Xiao-hong, Jia Xiao-y Similar articles in PubMed
[Study on three common mitochondrial DNA mutations in Leber's hereditary optic neuropathy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012 Oct 29 (5): 519-23. Ma Yun-xia, Zhou Yon-gan, Zhang Jing-ping, Zhang Quan-bin, Liu Wei-la, Ren Cai-fen, Li Xiao- Similar articles in PubMed
Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR. Clinica chimica acta; international journal of clinical chemistry 2010 Nov 411 (21-22): 1671-4. Bi Rui, Zhang A-Mei, Yu Dandan, Chen Diana, Yao Yong-Ga Similar articles in PubMed
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion 2010 Apr 10 (3): 300-8. Nishigaki Yutaka, Ueno Hitomi, Coku Jorida, Koga Yasutoshi, Fujii Tatsuya, Sahashi Ko, Nakano Kazutoshi, Yoneda Makoto, Nonaka Michiko, Tang Linya, Liou Chia-Wei, Paquis-Flucklinger Veronique, Harigaya Yasuo, Ibi Tohru, Goto Yu-ichi, Hosoya Hiroko, DiMauro Salvatore, Hirano Michio, Tanaka Masas Similar articles in PubMed
Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber's hereditary optic neuropathy. Eye (London, England) 2010 Jan 24 (1): 107-11. Seo J H, Hwang J-M, Park S Similar articles in PubMed
Gene-environment interactions in Leber hereditary optic neuropathy. Brain : a journal of neurology 2009 Sep 132 (Pt 9): 2317-26. Kirkman Matthew Anthony, Yu-Wai-Man Patrick, Korsten Alex, Leonhardt Miriam, Dimitriadis Konstantin, De Coo Ireneaus F, Klopstock Thomas, Chinnery Patrick Franc Similar articles in PubMed
Pathogenic mitochondrial DNA mutations are common in the general population. American journal of human genetics 2008 Aug 83 (2): 254-60. Elliott Hannah R, Samuels David C, Eden James A, Relton Caroline L, Chinnery Patrick Similar articles in PubMed
Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors. Archives of medical research 2006 Nov 37 (8): 1028-33. Shafa Shariat Panahi Mehdi, Houshmand Massoud, Tabassi Abdol Re Similar articles in PubMed
[Clinical features and the mutation of Leber's hereditary optic neuropathy in Chinese patients]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005 Jun 22 (3): 334-6. Wang Yan, Guo Xiang-ming, Jia Xiao-yun, Li Shi-qiang, Xiao Xue-shan, Guo Li, Zhang Qing-jio Similar articles in PubMed
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 Similar articles in PubMed
Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor? Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 0 19 (2): e21-7. Khatami Mehri, Houshmand Massoud, Sadeghizadeh Majid, Eftekharzadeh Mahmood, Heidari Mohammad Mehdi, Saber Siamak, Banihashemi Kambiz, Scheiber-Mojdehkar Barba Similar articles in PubMed
Meta-analysis of the prevalence of Leber hereditary optic neuropathy mtDNA mutations in Europe. European journal of ophthalmology 0 22 (3): 461-5. Mascialino Barbara, Leinonen Mika, Meier Thom Similar articles in PubMed
Mitochondrial DNA mutations with Leber's hereditary optic neuropathy in Japanese patients with open-angle glaucoma. Japanese journal of ophthalmology 0 50 (2): 128-34. Inagaki Yoko, Mashima Yukihiko, Fuse Nobuo, Ohtake Yuichiro, Fujimaki Takuro, Fukuchi Takeo, Similar articles in PubMed

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