Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua

[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.