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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
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023
Pyruvate Dehydrogenase Deficiency (PDCD)
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017
Recommendations for the Management of Strokelike Episodes in Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes
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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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Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Inclusion Body Myositis and Myopathies
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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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