Prevalence and genotypic associations of epilepsy in Prader-Willi Syndrome: A systematic review and meta-analysis-Reference-Cited by-同舟云学术

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Prevalence and genotypic associations of epilepsy in Prader-Willi Syndrome: A systematic review and meta-analysis

Published:2024-06 Issue: Volume:155 Page:109803
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Pascual-Morena Carlos,Martínez-Vizcaíno Vicente,Cavero-Redondo Iván,Álvarez-Bueno Celia,Martínez-García Irene,Rodríguez-Gutiérrez Eva,Otero-Luis Iris,del Saz-Lara Andrea,Saz-Lara Alicia

Funder

Universidad de Castilla-La Mancha

España Ministerio de Ciencia Innovación y Universidades

Publisher

Elsevier BV

Reference53 articles.

1. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings;Angulo;J Endocrinol Invest,2015

2. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes;Kalsner;Pediatr Clin North Am,2015

3. Prader-Willi syndrome;Driscoll;Neuropediatrics,2023

4. Feasibility of screening for chromosome 15 imprinting disorders in 16 579 newborns by using a novel genomic workflow;Godler;JAMA Netw Open,2022

5. Prader-Willi syndrome;Cassidy;Genet Med,2012

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