2Goto Y,Tojo M,Tohyama J,et al.A novel point mutation in the mitochondrial tRNA (Leu)(UUR) gene in a family with mitochondrial myopathy[J].Ann Neurol,1992,31:672-675.
3Goto Y,Horai S,Matsuoka T,et al.Mitochondrial myopathy,encephalopathy,lactic acidosis,and stroke -like episodes (MELAS):a correlative study of the clinical features and mitochondrial DNA mutation[J].Neurology,1992,42:545-550.
4Iizuka T,Sakai F,Suzuki N,et al.Neuronal hyperexcitability in stroke-like episodes of MELAS syndrome[J].Neurology,2002,59:816-824.
5Iizuka T,Sakai F,Kan S,et al.Slowly progressive spread of the stroke-like lesions in MELAS[J].Neurology,2003,61:1238-1244.
6Ohama E,Ohara S,Ikuta F,et al.Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy[J].Acta Neuropathol,1987,74:226-233.
7Kaufmann P,Shungu DC,Sano MC,et al.Cerebral lactic acidosis correlates with neurological impairment in MELAS[J].Neurology,2004,62:1297-1302.
8Iizuka T,Sakai F.Pathogenesis of Stroke-Like Episodes in MELAS:Analysis of Neurovascular Cellular Mechanisms[J].Current Neurovascular Research,2005,2:29-45.
9Feddersen B,Bender A,Arnold S,et al.Aggressive confusional state as a clinical manifestation of status epilepticus in MELAS[J].Neurology,2003,61:1149-1150.
10Cock H,Schapira AHV.Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy[J].Epilepsia,1999,40(Suppl 3):33-40.