EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome-Reference-Cited by-同舟云学术

EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome

Published:2010-05 Issue:5 Volume:121 Page:652-657
ISSN:1388-2457
Container-title:Clinical Neurophysiology
language:en
Short-container-title:Clinical Neurophysiology

Author:

Buoni Sabrina,Zannolli Raffaella,De Felice Claudio,De Nicola Anna,Guerri Vanessa,Guerra Beatrice,Casali Stefania,Pucci Barbara,Corbini Letizia,Mari Francesca,Renieri Alessandra,Zappella Michele,Hayek Joseph

Publisher

Elsevier BV

Subject

Physiology (medical),Clinical Neurology,Neurology,Sensory Systems

Reference20 articles.

1. Correlation between clinical severity in Rett syndrome patients with a p.R168X or p.T158M MECP2 mutation and the direction and degree of skewing of X chromosome inactivation;Archer;J Med Genet,2007

2. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2-mutated Rett syndrome;Buoni;Clin Neurophysiol,2008

3. Systemic oxidative stress in classic Rett syndrome;De Felice;Free Radic Biol Med.,2009

4. International League Against Epilepsy (ILAE) A proposed diagnostic scheme for people with epileptic seizures and with epilepsy report of the ILAE task force on classification and terminology;Engel;Epilepsia,2001

5. Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE);Fisher;Epilepsia,2005

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