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Showing articles 0 to 9 of 9 Filter Applied: Leigh's disease (Click to remove) 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 Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011 Bilateral Thalamic Lesions AJR 192:W53-W62, Smith,A.B.,et al, 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 Progressive Dystonia with Bilateral Putaminal Hypodensities Arch Neurol 44:1184-1187, Berkovic,S.F.,et al, 1987 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Showing articles 0 to 9 of 9