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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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A 53-year-old Woman with Lower Extremity Paresthesias
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 10-year-old boy with Bilateral Vision Loss
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MR Neurography for the Diagnosis of Hypertrophic Neuropathies
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A Young Man with Progressive Vision and Hearing Loss
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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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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Autonomic Peripheral Neuropathy
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Cardiac Dysfunction in Neuromuscular Diseases
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Niemann-Pick Disease Type C from Bench to Bedside
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Monomelic Amyotrophy
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Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
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Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
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A Clinical Study of Noonan Syndrome
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Diagnostic Tests for Choreoacanthocytosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Cervical Dystonia:Clinical Findings and Associated Movement Disorders
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