Heterogeneity of Coenzyme Q10 Deficiency
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Mitochondrial DNA and Disease
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Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Recommendations for the Management of Strokelike Episodes in Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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MELAS
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Metabolic Disease and Stroke: MELAS
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial Optic Neuropathies
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Parkinson's Disease
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Inclusion Body Myositis and Myopathies
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Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
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Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
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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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Adult Reye's Syndrome:A Review with New Evidence for a Generalized Defect in Intramitochondrial Enzyme Processing
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Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
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Mitochondrial DNA and Genetic Disease
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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