Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua
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R. Ferri | M. Elia | S. Musumeci | V. Colamaria | D. Greco | M. C. Stefanini | G. Azan
[1] S. Dimauro,et al. The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome , 1993, Annals of neurology.
[2] Jean Aicardi,et al. Diseases of the Nervous System in Childhood , 1993 .
[3] R. Sakuta,et al. A T-to-G Mutation at Nucleotide Pair 8993 in Mitochondrial DNA in a Patient With Leigh's Syndrome , 1993, Journal of child neurology.
[4] S. Dimauro,et al. Maternally inherited Leigh syndrome. , 1993, The Journal of pediatrics.
[5] D. Schomer. Focal Status Epilepticus and Epilepsia Partialis Continua in Adults and Children , 1993, Epilepsia.
[6] C. Cunniff,et al. Variable presentation of cytochrome c oxidase deficiency. , 1992, American journal of diseases of children.
[7] M. Holzgraefe,et al. Diagnosis and treatment in a case of juvenile subacute necrotizing encephalopathy Leigh without cytochrome c oxidase deficiency. , 1992, European neurology.
[8] S. Dimauro,et al. Cytochrome c oxidase-associated Leigh syndrome: Phenotypic features and pathogenetic speculations , 1991, Journal of the Neurological Sciences.
[9] K. Leenders,et al. Epilepsia partialis continua studied by PET , 1991, Epilepsy Research.
[10] I. Nonaka,et al. [A case with MELAS associated with epilepsia partialis continua]. , 1991, No to hattatsu = Brain and development.
[11] B. Harding. Review Article: Progressive Neuronal Degeneration of Childhood With Liver Disease (Alpers-Huttenlocher Syndrome): A Personal Review , 1990, Journal of child neurology.
[12] J. R. Hughes,et al. Advances in epileptology , 1990 .
[13] S. Hilal,et al. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect. , 1990, AJR. American journal of roentgenology.
[14] M. Ito,et al. Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndrome. , 1990, The Journal of pediatrics.
[15] O. Dulac,et al. Kojewnikow's epilepsia partialis continua: Two cases associated with striatal necrosis , 1988, Neurophysiologie Clinique/Clinical Neurophysiology.
[16] L. de Meirleir,et al. Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease. , 1987, The Journal of pediatrics.
[17] B. Berg,et al. Magnetic resonance imaging in subacute necrotizing encephalomyelopathy (Leigh's disease) , 1986, Annals of neurology.
[18] J. Pincott,et al. Cortical subacute necrotizing encephalomyelopathy. A study of two patients with mitochondrial dysfunction. , 1984, Neuropediatrics.
[19] J. Gilroy,et al. Mitochondrial myopathy and encephalopathy , 1983, Neurology.
[20] H. Gröbe,et al. SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY , 1975, Acta paediatrica Scandinavica.
[21] D. Leigh. SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANT , 1951, Journal of neurology, neurosurgery, and psychiatry.