Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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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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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Metabolic Disease and Stroke: MELAS
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Mitochondrial DNA Polymerase-y and Human Disease
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Clinicopath Conf., MELAS Syndrome
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Mitochondrial Respiratory-Chain Diseases
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Mitochondrial DNA and Disease
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Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
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Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
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Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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