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Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
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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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Pediatric Leigh Syndrome
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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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Acute Leukoencephalopathies:Differential Diagnosis and Investigation
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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"Disappearing Infarct" Is Late-Onset MELAS
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A Young Man with Progressive Vision and Hearing Loss
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Clinico-Radiological Spectrum of Bilateral Temporal Lobe Hyperintensity: A Retrospective Review
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Mitochondrial Dysfunction in Multiple Symmetrical Lipomatosis
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Mitochondrial DNA and Genetic Disease
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A Defect in Mitochondrial Electron-Transport Activity in Leber's Hereditary Optic Neuropathy
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Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
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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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