Showing results (651-660 of 675) with videos related to

Sort By:
Pageof 68
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2018
The landscape of epilepsy-related GATOR1 variantsSara Baldassari, Fabienne Picard, Nienke E Verbeek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction to: The landscape of epilepsy-related GATOR1 variantsSara Baldassari, Fabienne Picard, Nienke E Verbeek, et al.
Human Mutation|January 6, 2022
Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiencyMarcello Scala, Saskia B Wortmann, Namik Kaya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2018
Correction: The landscape of epilepsy-related GATOR1 variantsSara Baldassari, Fabienne Picard, Nienke E Verbeek, et al.
Epilepsia|June 3, 2022
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional dataSeymour M Lopez, Leon M Aksman, Neil P Oxtoby, et al.
Brain : a Journal of Neurology|March 25, 2022
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsyBo-Yong Park, Sara Larivière, Raul Rodríguez-Cruces, et al.
Nature Communications|July 14, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Christine L Dixon, Hui Guo, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
A WORLDWIDE ENIGMA STUDY ON EPILEPSY-RELATED GRAY AND WHITE MATTER COMPROMISE ACROSS THE ADULT LIFESPANJudy Chen, Alexander Ngo, Raúl Rodríguez-Cruces, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Brain : a Journal of Neurology|January 25, 2018
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA studyChristopher D Whelan, Andre Altmann, Juan A Botía, et al.
Pageof 68