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Mitochondrial DNA and Disease
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Mitochondrial Disease and Stroke
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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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Inclusion Body Myositis and Myopathies
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Ophthalmologic Manifestations in MELAS Syndrome
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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MELAS Syndrome Involving a Mother & Two Children
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"Disappearing Infarct" Is Late-Onset MELAS
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Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
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Longitudinally Extensive Transverse Myelitis in MELAS
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Pediatric Leigh Syndrome
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Pyruvate Dehydrogenase Deficiency (PDCD)
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A Young Man with Progressive Vision and Hearing Loss
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Epilepsy in Adults with Mitochondrial Disease: A Cohort Study
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Heterogeneity of Coenzyme Q10 Deficiency
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Alzheimers Disease
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Mitochondrial DNA Polymerase-y and Human Disease
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Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
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