No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1-Reference-Cited by-同舟云学术

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No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1

Published:1999-12 Issue:12 Volume:40 Page:1799-1803
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Gennaro Elena,Malacarne Michela,Carbone Ilaria,Riggio Maria Concetta,Bianchi Amedeo,Bonanni Paolo,Boniver Clementina,Bernardina Bernardo Dalla,Marco Pasquale,Giordano Lucio,Guerrini Renzo,Santorum Enrica,Sebastianelli Rosella,Vecchi Marilena,Veggiotti Pierangelo,Vigevano Federico,Bricarelli Franca Dagna,Zara Federico

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1157.1999.tb01601.x/fullpdf

Reference19 articles.

1. Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder

2. Benign Familial Neonatal Convulsions

3. Benign infantile familial convulsions

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy;Annals of Neurology;2014-05-20

2. Idiopathic focal epilepsies;Handbook of Clinical Neurology;2013

3. Idiopathic epileptic seizures and syndromes in infancy;A Clinical Guide to Epileptic Syndromes and their Treatment;2010

4. Benign Infantile Seizures or Watanabe–Vigevano Syndrome;Atlas of Epilepsies;2010

5. The spectrum of benign infantile seizures;Epilepsy Research;2006-08

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