Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study-Reference-Cited by-同舟云学术

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Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study

Published:2024-09 Issue: Volume:205 Page:107399
ISSN:0920-1211
Container-title:Epilepsy Research
language:en
Short-container-title:Epilepsy Research

Author:

Yıldız Nihal,Serdaroğlu Esra,Kart Pınar Özkan,Besen Seyda,Kanmaz Seda,Toprak Dilara Ece,Kilic Betul,Ersoy Ozlem,Gencpinar Pınar,Dundar Nihal Olgac,Okuyaz Cetin,Serdaroglu Ayse,Carman Kursat Bora,Yarar Coşkun,Ekici Barış,Tatlı Burak,Erol İlknur,Aydın Kürşad,Tekgül Hasan,Cansu Ali

Publisher

Elsevier BV

Reference25 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. FOXG1 is responsible for the congenital variant of Rett syndrome;Ariani;Am. J. Hum. Genet.,2008

3. Oral findings in Rett syndrome: an update and review of the literature;Bianco;Dent. Med Probl.,2018

4. Rett Syndrome. 2023 Aug 8;Chahil,2023

5. Rett syndrome and epilepsy: an update for child neurologists;Dolce;Pediatr. Neurol.,2013

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