Epilepsy in a cohort of children with Noonan syndrome and related disorders
Chiara Davico(Centro Studi GISED), Giovanni Battista Ferrero(5T Torino (Italy)), Roberta Vittorini(University of Turin), Marta Borgogno(Centro Studi GISED), Federico Amianto(University of Turin), Diana Carli(University of Turin), Alessandro Mussa(Unknown), Filippa Campagna, Rossella D’Alessandro(University of Turin), Benedetto Vitiello(University of Turin), Federica Ricci(University of Turin)
Cited by 13
Related Papers
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
|Nature Genetics|2022|613
Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
|Nature Reviews Endocrinology|2018|596
Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
|Nature Genetics|2009|417
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
|Nature Communications|2019|249
Pandemic-related emergency psychiatric presentations for self-harm of children and adolescents in 10 countries (PREP-kids): a retrospective international cohort study
|European Child & Adolescent Psychiatry|2021|118