Literature DB >> 16279991

Charcot-Marie-Tooth disease due to the Thr124Met mutation in the myelin protein zero gene associated with multiple sclerosis.

Yusuf A Rajabally, Richard J Abbott.   

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Year:  2005        PMID： 16279991     DOI： 10.1111/j.1085-9489.2005.00054.x

Source DB:  PubMed          Journal:  J Peripher Nerv Syst        ISSN： 1085-9489            Impact factor:   3.494


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  4 in total

1.  Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis.

Authors:  D H Kilfoyle; P J Dyck; Y Wu; W J Litchy; D M Klein; P J B Dyck; N Kumar; J M Cunningham; C J Klein
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-08       Impact factor: 10.154

Review 2.  The sad plight of multiple sclerosis research (low on fact, high on fiction): critical data to support it being a neurocristopathy.

Authors:  Peter O Behan; Abhijit Chaudhuri
Journal:  Inflammopharmacology       Date:  2010-09-24       Impact factor: 5.093

3.  A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B.

Authors:  Rosa Cortese; Stefano Zoccolella; Maria Muglia; Alessandra Patitucci; Antonio Scarafino; Damiano Paolicelli; Isabella Laura Simone
Journal:  Brain Behav       Date:  2016-09-25       Impact factor: 2.708

4.  Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.

Authors:  Oranee Sanmaneechai; Shawna Feely; Steven S Scherer; David N Herrmann; Joshua Burns; Francesco Muntoni; Jun Li; Carly E Siskind; John W Day; Matilde Laura; Charlotte J Sumner; Thomas E Lloyd; Sindhu Ramchandren; Rosemary R Shy; Tiffany Grider; Chelsea Bacon; Richard S Finkel; Sabrina W Yum; Isabella Moroni; Giuseppe Piscosquito; Davide Pareyson; Mary M Reilly; Michael E Shy
Journal:  Brain       Date:  2015-08-25       Impact factor: 13.501
  4 in total

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