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Mitochondrial Therapy for Parkinson Disease
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Parkinson's Disease
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Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
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Mitochondrial Involvement in Parkinson's Disease:The Controversy Continues
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Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
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Mitochondrial Oxidative Phosphorylation Defects in Parkinson's Disease
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Pediatric Leigh Syndrome
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Clinico-Radiological Spectrum of Bilateral Temporal Lobe Hyperintensity: A Retrospective Review
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Adult-Onset MELAS Presenting as Herpes Encephalitis
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Recurrent Strokes in a 34-Year-Old Man
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Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Mitochondrial Dysfunction in Multiple Symmetrical Lipomatosis
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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