4Medina L, Chi TL, DeVivo DC ,et al. MR Wndings in patients with subacute necrotizing encephalomyelopathy ( Leigh syndrome) : correlation with biochemical defect. AJR, 1990,154 : 1269.
5Savoiardo M, Uziel G, Strada L, et al. MRI Wndings in Leigh disease with cytochrome c-oxidase deWciency. Neuroradiology, 1991,33:507.
6Barkovich A J, Good WV, Koch TK, et al. Mitochondrial disorders : analysis of their clinical and imaging characteristics. AJNR, 1993,14: 1119.
7Benit P, Slama A, Cartault F, et al. Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome. J Med Genet, 2004, 41(1): 14-17.
8Naess K, Freyer C, Bruhn H, et al. MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome. Biochim Biophys Acta, 2009, 1787(5): 484-490.
9Ashrafi MR, Ghofrani M, Ghojevand N. Leigh syndrome: clinical and paraclinical study. Acta Medica Iranica, 2002, 40(4): 236-240.
10Sakushima K, Tsuji-Akimoto S, Niino M, et al. Adult leigh disease without failure to thrive. Neurologist, 2011, 17(4): 222-227.
