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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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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Pyruvate Dehydrogenase Deficiency (PDCD)
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
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Heterogeneity of Coenzyme Q10 Deficiency
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine
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Mitochondrial Respiratory-Chain Diseases
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
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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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Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
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