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Showing articles 0 to 10 of 10 Filter Applied: Leigh's disease (Click to remove) Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 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 A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia Neurol 72:1262-1276, DiMauro,S.,et al, 2009 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Bilateral Thalamic Lesions AJR 192:W53-W62, Smith,A.B.,et al, 2009 Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia NEJM 359:1156-1166, Case 28-2008, 2008 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members Ann Neurol 3:519, Whetsell,W.O.,et al, 1978 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Showing articles 0 to 10 of 10