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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Mitochondrial DNA Polymerase-y and Human Disease
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Neurologic Aspects of Inflammatory Bowel Disease
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Mitochondrial DNA and Disease
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
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Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
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A Woman with Progressive Painless Sequential Monocular Vision Loss
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Bilateral Hearing Loss and Constricted Visual Fields
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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A Young Woman with Respiratory Failure, Hearing Loss, and Paraplegia
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A 37-Year-Old Man with Multiple Cranial Neuropathies
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Intracranial Neoplasms and Paraneoplastic Disorders, Carcinomatous Meningitis
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Heterogeneity of Coenzyme Q10 Deficiency
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Neurobrucellosis:Clinical and Neuroimaging Correlation
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Mitochondrial Respiratory-Chain Diseases
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Syndrome of Orthostatic Headaches and Diffuse Pachymeningeal Gadolinium Enhancement
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Cockayne Syndrome: Review of 140 Cases
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Anderson-Fabry Disease
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Acute Sensorineural Deafness in Lassa Fever
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Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
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Heredopathia Atactica Polyneuritiformis
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Kearns-Sayre Syndrome & Hypoparathyroidism
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Neurological Manifestations of Fabry Disease in Female Carriers
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Lymphomatoid Granulomatosis Clinically Confined to the CNS
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Important Advances in Clinical Medicine
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