Mitochondrial DNA and Disease
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A Young Man with Progressive Vision and Hearing Loss
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MELAS
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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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
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999
Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
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Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
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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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Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
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MELAS Syndrome Involving a Mother & Two Children
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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