Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions-Reference-Cited by-同舟云学术

Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions

Published:2011-08-17 Issue:8 Volume:6 Page:e23182
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Kasperavičiūtė Dalia,Catarino Claudia B.,Chinthapalli Krishna,Clayton Lisa M. S.,Thom Maria,Martinian Lillian,Cohen Hannah,Adalat Shazia,Bockenhauer Detlef,Pope Simon A.,Lench Nicholas,Koltzenburg Martin,Duncan John S.,Hammond Peter,Hennekam Raoul C. M.,Land John M.,Sisodiya Sanjay M.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference38 articles.

1. Epilepsy: being ill in more ways than one.;S Wiebe;Epilepsy Curr,2007

2. The epidemiology of the comorbidity of epilepsy in the general population.;A Gaitatzis;Epilepsia,2004

3. Migraine, epilepsy, and psychiatric comorbidity: partners in crime.;MR Winawer;Neurology,2010

4. Treating obstructive sleep apnea in adults with epilepsy: a randomized pilot trial.;BA Malow;Neurology,2008

5. Neurological comorbidity and epilepsy: implications for treatment.;G Zaccara;Acta Neurol Scand,2009

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