Metabolic Disease and Stroke: MELAS
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Alternate-Sided Homonymous Hemianopia as the Solitary Presentation of Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes Syndrome
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Magnetic Resonance Imaging Shows Specific Abnormalities in the MELAS Syndrome
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Magnetic Resonance Imaging in MELAS Syndrome
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Pediatric Leigh Syndrome
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Multiple Simultaneous Cerebral Infarctions in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002
Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
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Mitochondrial DNA and Disease
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Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies
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Significance of Basal Ganglia Calcification on Computed Tomography in Children
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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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