Charcot-Marie-Toothdisease相关论文
Objective: The aim of the present study was to investigate the molecular genetic characterstics of Charcot-Marie-Tooth (......
Mutation analysis of MPZ gene and clinical features in Chinese patients with Charcot-Marie-Tooth dis
Background and objective Charcot-Marie-Tooth disease (CMT), also called hereditary motor and sensory neuropathy (HMSN), ......
Two rare mutations in exon 3 and 5 of HSG/MFN2 gene may dance together in the mixed style of essenti
Vascular proliferative disorders,such as atherosclerosis and restenosis,are the most common causes of severe cardiovascu......
Nine-hole Peg Test and Ten-meter Walk Test for Evaluating Functional Loss in Chinese Charcot-Marie-T
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Clinical classification and gene mutation of Chinese probands with Charcot-Marie-Tooth disease Analy
Charcot-Mafie-Tooth (CMT) disease is the most common inherited peripheral neuropathic disorder.CMT is clinically and gen......
Rapid genetic screening of Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liabil
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Objective: Apparently, scoliosis occurs in approximately one-third of patients with Charcot-Marie-Tooth disease. Little ......
Genetic factors may be learnt from families with gene mutations that render nerve-injury sus-ceptibility even to ordinar......