Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
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Neurogenic Muscle Hypertrophy
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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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Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
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