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Showing articles 0 to 11 of 11 Filter Applied: neurologic disease,diagnoses of (Click to remove) MR Neurography for the Diagnosis of Hypertrophic Neuropathies Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017 Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy NEJM 362:1181-1191, Lupski,J.R., et al, 2010 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 PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A Neurol 50:760-763, Young,P.,et al, 1998 Inherited Primary Peripheral Neuropathies JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993 Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1) Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992 Clinical Manifestations and Evaluation of Adults with Suspected Native Valve Endocarditis UpToDate Feb, Sexton, D.J. & Fowler,Jr., V.G., 2016 Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy Neurol 55:527-532, Gilman,S. et al, 2000 Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy JNNP 65:65-71, Schrag,A.,et al, 1998 Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families Neurol 51:1666-1671, Moseley,M.L.,et al, 1998 Trinucleotide Repeat Expansion in Neurological Disease Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994 Showing articles 0 to 11 of 11