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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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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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Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
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Atrophy of Bilateral Extraocular Muscles
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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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Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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A 31-Year-Old Man with Sequential Vision Loss
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Pediatric Leigh Syndrome
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Rapidly Progressive Leukoencephalopathy in Mitochondrial Complex I Deficiency
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Heterogeneity of Coenzyme Q10 Deficiency
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Clinicopath Conf., MELAS Syndrome
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Mitochondrial Respiratory-Chain Diseases
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A Forearm Exercise Screening Test for Mitochondrial Myopathy
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Mitochondrial Optic Neuropathies
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Mitochondrial Disease and Stroke
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Recurrent Strokes in a 34-Year-Old Man
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Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Late-Onset Mitochondrial Myopathy
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Inclusion Body Myositis and Myopathies
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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