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Showing articles 0 to 12 of 12 Filter Applied: Charcot-Marie-Tooth (Click to remove) Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I Neurol 39:1173-1177, Rosen,S.A.,et al, 1989 A 53-year-old Woman with Lower Extremity Paresthesias Neurol 94:1105-1108, Dehbashi, S.,et al, 2020 Chronic and Slowly Progressive Weakness of the Legs and Hands BMJ 348:g459, Nightingale, H.,et al, 2014 Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias Neurol 74:775-778, Karam,C. &Scelsa,S., 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 Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging AJNR 25:494-497, Aho,T.R.,et al, 2004 MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000 Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A Neurol 52:890-891, Butefisch,C.,et al, 1999 Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy JNNP 67:685-687, Duarte,J.,et al, 1999 Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995 Neurotoxicity of Commonly Used Antineoplastic Agents NEJM 291:75, 1271974., Weiss,H.,et al, 1974 Diseases of Muscles-Clinical Manifestations & Differential Diagnosis The New Physic 263, 1967, Oct., Boshes,L., 1967 Showing articles 0 to 12 of 12