Showing results (131-140 of 330) with videos related to
Sort By:
Pageof 33
Epilepsia|June 23, 2011
A retrospective population-based study on seizures related to childhood vaccinationSarah von Spiczak, Ingo Helbig, Ursula Drechsel-Baeuerle, et al.Epilepsia|February 19, 2015
Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysisCorinna Hartmann, Sarah von Spiczak, Arvid Suls, et al.Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Shared and distinct phenotypic profiles among neurodevelopmental disorder genesHermela Shimelis, Matthew T Oetjens, Bobbi McGivern, et al.Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Early life seizures and epileptic spasms in <i>STXBP1</i>-related disordersKim M Thalwitzer, Julie Xian, Danielle deCampo, et al.Epilepsia|May 5, 2021
Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractableDavid Lewis-Smith, Peter D Galer, Ganna Balagura, et al.Medrxiv : the Preprint Server for Health Sciences|March 23, 2026
Characterizing <i>SCN1A</i> -Related Disorders Using Real-World Data Across 681 Patient-YearsAnna J Prentice, Ian McSalley, Jan H Magielski, et al.Epilepsia|January 27, 2024
Early life seizures and epileptic spasms in STXBP1-related disordersKim M Thalwitzer, Julie Xian, Danielle de Campo, et al.Brain : a Journal of Neurology|October 16, 2024
The clinical and genetic spectrum of paediatric speech and language disordersJan H Magielski, Sarah M Ruggiero, Julie Xian, et al.Epilepsy Research|March 27, 2010
Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysisHiltrud Muhle, Sarah von Spiczak, Verena Gaus, et al.Nature Communications|July 20, 2023
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individualsLudovica Montanucci, David Lewis-Smith, Ryan L Collins, et al.Pageof 33