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Showing articles 0 to 15 of 15 Filter Applied: mitochondrial disease (Click to remove) Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 Imaging Patterns Characterizing Mitochondrial Leukodystrophies AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021 Pediatric Leigh Syndrome Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020 A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017 A Young Man with Progressive Vision and Hearing Loss JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia Neurol 72:1262-1276, DiMauro,S.,et al, 2009 Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex Clin Radiol 63:1245-1253, Sheerin,F.,et al, 2008 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Clinicopath Conf., MELAS Syndrome NEJM 353:2271-2280, Case 36-2005, 2005 Acute Leukoencephalopathies:Differential Diagnosis and Investigation The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998 Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis JNNP 65:233-240, Sue,C.M.,et al, 1998 Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993 Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT Neurol 34:1456-1460, Yamamoto,T.,et al, 1984 Showing articles 0 to 15 of 15