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Showing articles 0 to 10 of 10 Filter Applied: neuropathy,hereditary peripheral (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Strokelike Episodes in a Patient with Chronic Gait Abnormalities JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019 Clinical Reasoning: A Teenager with Left Arm Weakness Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018 MR Neurography for the Diagnosis of Hypertrophic Neuropathies Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017 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 The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease Neurol 61:1475-1478, Taylor,R.A.,et al, 2003 Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study Ann Neurol 28:43-49, Claus,D.,et al, 1990 Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I Neurol 39:1173-1177, Rosen,S.A.,et al, 1989 Refsum Disease In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989 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 10 of 10