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Mitochondrial DNA and Disease
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The Polymerase Chain Reaction:Application to Nervous System Disease
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Pediatric Leigh Syndrome
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Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
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The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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Progressive Dystonia with Bilateral Putaminal Hypodensities
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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