Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygousCSTBpoint and indel mutations-Reference-Cited by-同舟云学术

Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygousCSTBpoint and indel mutations

Published:2012-12 Issue:12 Volume:53 Page:2120-2127
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Canafoglia Laura,Gennaro Elena,Capovilla Giuseppe,Gobbi Giuseppe,Boni Antonella,Beccaria Francesca,Viri Maurizio,Michelucci Roberto,Agazzi Pamela,Assereto Stefania,Coviello Domenico A.,Di Stefano Maria,Rossi Sebastiano Davide,Franceschetti Silvana,Zara Federico

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2012.03718.x/fullpdf

Reference24 articles.

1. Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations;Alakurtti;Eur J Hum Genet,2005

2. Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease;Canafoglia;Neurology,2004

3. Long-term evolution of EEG in Unverricht-Lundborg disease;Ferlazzo;Epilepsy Res,2007

4. Neuropsychological findings in patients with Unverricht-Lundborg disease;Ferlazzo;Epilepsy Behav,2009

5. Unverricht-Lundborg disease (EPM1);Genton;Epilepsia,2010

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