The Broad Clinical Spectrum of Epilepsies Associated With Protocadherin 19 Gene Mutation
Giovanni Battista Dell’Isola(Saint Camillus International University of Health and Medical Sciences), Alberto Verrotti(University of Perugia), Valerio Vinti(University of Perugia), Giorgia Tascini(University of Perugia), Antonella Fattorusso(University of Perugia), Giuseppe Di Cara(University of Perugia), Pasquale Striano(Istituto Giannina Gaslini), Elisabetta Mencaroni(University of Perugia)
Cited by 35
Related Papers
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
|New England Journal of Medicine|2008|811
Autism Spectrum Disorders and the Gut Microbiota
|Nutrients|2019|479
The Pharmacoresistant Epilepsy: An Overview on Existent and New Emerging Therapies
|Frontiers in Neurology|2021|260
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
|Nature Communications|2019|248
Defining the phenotypic spectrum of <i>SLC6A1</i> mutations
|Epilepsia|2018|151