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A Young Man with Progressive Vision and Hearing Loss
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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MELAS Syndrome Involving a Mother & Two Children
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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"Disappearing Infarct" Is Late-Onset MELAS
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Mitochondrial Optic Neuropathies
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Age and Cause of Death in Mitochondrial Diseases
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
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Atrophy of Bilateral Extraocular Muscles
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Mitochondrial DNA and Disease
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Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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