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Showing articles 0 to 11 of 11 Filter Applied: Leigh's disease (Click to remove) A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia Neurol 72:1262-1276, DiMauro,S.,et al, 2009 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016 Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease) Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome) Ann Neurol 6:200-206, Kalimo,H.,et al, 1979 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Showing articles 0 to 11 of 11