A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Mitochondrial DNA and Disease
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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MELAS
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Mitochondrial Respiratory-Chain Diseases
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Mitochondrial Optic Neuropathies
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Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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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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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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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
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A 31-Year-Old Man with Sequential Vision Loss
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
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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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A Young Man with Progressive Vision and Hearing Loss
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The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
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Serial Diffusion Imaging in a Case of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
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Metabolic Disease and Stroke: MELAS
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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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Adult-Onset MELAS
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Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Ophthalmologic Manifestations in MELAS Syndrome
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A Defect in Mitochondrial Electron-Transport Activity in Leber's Hereditary Optic Neuropathy
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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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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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