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Showing articles 0 to 6 of 6 Filter Applied: neuropathy,hereditary peripheral (Click to remove) Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene NEJM 354:2584-2592, Case 18-2006, 2006 Clinical Spectrum of Chronic Acquired Demyelinating Polyneuropathies Muscle & Nerve 24:311-324, Saperstein,D.S.,et al, 2001 Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy BMJ 316:1500-1501, Ando,Y.,et al, 1998 Molecular Genetics of Amyloid Neuropathy in Europe Lancet 1:524-526, Holt,I.J.,et al, 1989 Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988 Scalloped Pupils in Familial Amyloidosis NEJM 293:914, Lessell,S.,et al, 1975 Showing articles 0 to 6 of 6