Showing results (1-10 of 24) with videos related to
Sort By:
Pageof 3
The Lancet. Neurology|March 22, 2025
Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategiesRenzo Guerrini, Ingrid Scheffer, Simona BalestriniDevelopmental Medicine and Child Neurology|September 23, 2014
Lamotrigine can be beneficial in patients with Dravet syndromeLinda Dalic, Saul A Mullen, Eliane Roulet Perez, et al.Journal of Child Neurology|March 27, 2012
Benign neonatal sleep myoclonus: an autosomal dominant form not allelic to KCNQ2 or KCNQ3Zaid Afawi, Haim Bassan, Sarah Heron, et al.Autism Research : Official Journal of the International Society for Autism Research|December 1, 2023
Endophenotyping social cognition in the broader autism phenotypeEmmanuel Peng Kiat Pua, Tarishi Desai, Cherie Green, et al.Epilepsy Research|April 21, 2018
Early mortality in SCN8A-related epilepsiesKatrine M Johannesen, Elena Gardella, Ingrid Scheffer, et al.Orphanet Journal of Rare Diseases|June 12, 2023
Expanding genotype-phenotype correlations in FOXG1 syndrome: results from a patient registryElise Brimble, Kathryn G Reyes, Kopika Kuhathaas, et al.Neurology|August 28, 2025
<i>WWOX</i>-Related Developmental and Epileptic Encephalopathy: Expanding the Clinical Spectrum and Deciphering the Genotype-PhenotypeKelley Gao, Lisa G Riley, Jacques Raubenheimer, et al.Neurology. Genetics|April 12, 2016
Epilepsy with auditory features: A heterogeneous clinico-molecular diseaseTommaso Pippucci, Laura Licchetta, Sara Baldassari, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|June 22, 2010
Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy familyDimitar N Azmanov, Sashka Zhelyazkova, Petya S Dimova, et al.Stem Cell Research|August 16, 2019
Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum DisorderKiymet Bozaoglu, Yujing Gao, Edouard Stanley, et al.Pageof 3