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Showing articles 0 to 12 of 12 Filter Applied: mitochondrial disease (Click to remove) Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Melas Syndrome Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025 Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 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 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine AJNR 26:695-701,687, Tardieu,M.,et al, 2005 Acute Leukoencephalopathies:Differential Diagnosis and Investigation The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998 Parkinson's Disease NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998 Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy Lancet 337:508-510, Arnaudo,E.,et al, 1991 Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction Ann Neurol 29:606-614, Mhiri,C.,et al, 1991 Adult Reye's Syndrome:A Review with New Evidence for a Generalized Defect in Intramitochondrial Enzyme Processing Neurol 41:1815-1821, VanCoster,R.N.,et al, 1991 Showing articles 0 to 12 of 12