A 53-year-old Woman with Lower Extremity Paresthesias
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A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
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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 60-year-old man with arm weakness and numbness
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A Child with Delayed Motor Milestones and Ptosis
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Congenital Myasthenic Syndromes
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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A 54-year-old man with Dyspnea and Muscle Weakness
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Clinical Reasoning: A Teenager with Left Arm Weakness
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Essential Tremor
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MR Neurography for the Diagnosis of Hypertrophic Neuropathies
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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A 52-year-old Woman with Progressive Proximal Weakness
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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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Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Bent Spine Syndrome
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Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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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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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Autosomal Dominant Cramping Disease
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Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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The Oculopharyngeal Syndrome
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Complex Ataxia
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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