[1] Pauli W, Zarzycki A,Krzysztalowski A,et al.CT and MRI imaging of the brain in MELAS syndrome[J].Pol J Radiol,2013, 78(3):61-65. [2] Abe K, Yoshimura H,Tanaka H,et al.Comparison of conventional and diffusion-weighted MRI and proton MR spectroscopy in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like events[J].Neuroradiology,2004, 46(2):113-117. [3] Lee MH,Sung YJ,Yoon JH,et al.Wolff-Parkinson-white syndrome in a patient with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome[J].Korean Circ J,2011, 41(11):674-676. [4] Liu Y, Xue J,Zhao D,et al.Audiological evaluation in Chinese patients with mitochondrial encephalomyopathies[J].Chin Med J (Engl),2014,127(12):2304-2309. [5] Hirano M, Ricci E, Koenigsberger MR,et al.Melas: an original case and clinical criteria for diagnosis[J].Neuromuscul Disord,1992, 2(2):125-135. [6] Wang K, Takahashi Y, Gao ZL,et al. Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia[J].Neurogenetics,2009, 10(4):337-345. [7] Zhang J,Guo J, Fang W,et al.Clinical features of MELAS and its relation with A3243G gene point mutation[J].Int J Clin Exp Pathol,2015, 8(10):13411-13415. [8] Wang Z, Liu S,Yang Y,et al. Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS[J].Chin Med J (Engl),2002,115(7): 995-997. [9] Yamamoto M. Did de novo MELAS common mitochondrial DNA point mutation (mtDNA 3243, A-->G transition) occur in the mother of a proband of a Japanese MELAS pedigree[J].J Neurol Sci,1996,135(1):81-84. [10] Goto Y, Nonaka I,Horai S.A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies[J]. Nature,1990,348(6302):651-653. |