Differential (Click to cross reference) ataxia ataxia, cerebellar cerebrospinal fluid, lactic acid concentration children chromosomal abnormality chronic progressive external ophthalmoplegia dementia, transmissible encephalopathy epilepsia partialis continua gene gene mutation genetic neurologic disorders hepatic failure hepatolenticular degeneration, non-Wilsonian Jakob-Creutzfeldt disease Leigh's disease liver disease mitochondrial disease mitochondrial encephalomyopathy molecular genetics mortality muscle pain myoclonic jerks myopathy neuropathology ophthalmoplegia ophthalmoplegia, progressive external Parkinsonism syndrome POLG1 gene polymerase chain reaction progressive infantile poliodystrophy psychomotor retardation pyruvate metabolism, abnormality of quadriparesis review article screening seizure sodium valproate sodium valproate, toxicity spongy degeneration of brain status epilepticus status epilepticus, recurrent

Showing articles 0 to 5 of 5 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities Ann Neurol 49:377-383, Darin,N.,et al, 2001 Early Childhood Hepatocerebral Degeneration Misdiagnosed as Valproate Hepatotoxicity Ann Neurol 32:767-775, Bicknese,A.R.,et al, 1992 Transmission of Alpers'Disease (Chr Prog Encephalopathy) Produces Exper Creutzfeldt-Jakob Disease in Hamsters Neurol 39:615-621, Manuelidis,E.E.,et al, 1989 Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981 Showing articles 0 to 5 of 5