Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.1997.tb00347.x/fullpdf
Reference44 articles.
1. Tomaculous neuropathy: a clinical and electrophysiological study in patients with and without 1.5 Mb deletion in chromosome 17p11.2;Amato;Muscle and Nerve,1996
2. Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological findings;Behse;Brain,1972
3. Mutation analysis of the MPZ, PMP22 and C × 32 genes in Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies patients with Spanish ancestry;Bort;Human Genetics,1997
4. Brachial plexus involvement in familar pressure-sensitive neuropathy: electrophysiological and morphological findings;Bosch;Annals of Neurology,1980
5. DNA deletion associated with hereditary neuropathy with liability to pressure palsies;Chance;Cell,1993
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1. Clinical and neurophysiological features of the hereditary neuropathy with liability to pressure palsy due to the 17p11.2 deletion;Arquivos de Neuro-Psiquiatria;2016-02
2. Screening of the 17p11.2–p12 region in a large cohort of patients with Charcot-Marie-Tooth (CMT) disease or hereditary neuropathy with liability to pressure palsies (HNPP);Journal of Applied Genetics;2009-09
3. PMP 22 Gene;Myelin Biology and Disorders;2004
4. Clinical and electrophysiologic features of HNPP patients with 17p11.2 deletion;Acta Neurologica Scandinavica;2003-08-28
5. Valeur diagnostique du profil neurophysiologique classique dans les différents phénotypes de la neuropathie héréditaire sensible à la pression;La Revue de Médecine Interne;2002-04
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