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Showing articles 0 to 4 of 4 Filter Applied: neuropathy,hereditary peripheral (Click to remove) The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease Neurol 61:1475-1478, Taylor,R.A.,et al, 2003 Strokelike Episodes in a Patient with Chronic Gait Abnormalities JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019 Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet Neurol 46:1133-1137, Pareyson,D.,et al, 1996 Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988 Showing articles 0 to 4 of 4