A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Clinicopath Conf., MELAS Syndrome
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Mitochondrial DNA and Disease
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From Stroke Workup to Mitochondrial Disease: A Case Report of MELAS
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MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
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Melas Syndrome
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Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021
"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021
Pediatric Leigh Syndrome
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Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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Pyruvate Dehydrogenase Deficiency (PDCD)
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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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Heterogeneity of Coenzyme Q10 Deficiency
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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 Optic Neuropathies
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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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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Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
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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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