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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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Clinical Reasoning: A Teenager with Left Arm Weakness
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A Child with Delayed Motor Milestones and Ptosis
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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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Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
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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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Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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Recurrent Acroparaesthesia During Febrile Infections
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
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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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Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
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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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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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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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Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
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Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
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Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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