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Rima Nabbout

Showing results (241-250 of 310) with videos related to

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Plos Genetics|February 14, 2009
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects femalesChristel Depienne, Delphine Bouteiller, Boris Keren, et al.
Epilepsia|October 23, 2025
A global perspective on transitioning from pediatric to adult care in epilepsyDanielle M Andrade, Nathalie Jetté, Ilakkiah Chandran, et al.
Journal of Clinical Medicine|June 6, 2019
Early Clinical Predictors of Autism Spectrum Disorder in Infants with Tuberous Sclerosis Complex: Results from the EPISTOP StudyRomina Moavero, Arianna Benvenuto, Leonardo Emberti Gialloreti, et al.
Epilepsia|February 27, 2024
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsiesDeclan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger, et al.
Annals of Clinical and Translational Neurology|July 25, 2020
Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?Romina Moavero, Katarzyna Kotulska, Lieven Lagae, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Brain Communications|November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformationsSandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.
Annals of Neurology|November 12, 2020
Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP TrialKatarzyna Kotulska, David J Kwiatkowski, Paolo Curatolo, et al.
Neurology|January 25, 2022
Development and Validation of a Prediction Model for Early Diagnosis of <i>SCN1A</i>-Related EpilepsiesAndreas Brunklaus, Eduardo Pérez-Palma, Ismael Ghanty, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
Pageof 31

Showing results (241-250 of 310) with videos related to

Sort By:
Pageof 31
Plos Genetics|February 14, 2009
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects femalesChristel Depienne, Delphine Bouteiller, Boris Keren, et al.
Epilepsia|October 23, 2025
A global perspective on transitioning from pediatric to adult care in epilepsyDanielle M Andrade, Nathalie Jetté, Ilakkiah Chandran, et al.
Journal of Clinical Medicine|June 6, 2019
Early Clinical Predictors of Autism Spectrum Disorder in Infants with Tuberous Sclerosis Complex: Results from the EPISTOP StudyRomina Moavero, Arianna Benvenuto, Leonardo Emberti Gialloreti, et al.
Epilepsia|February 27, 2024
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsiesDeclan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger, et al.
Annals of Clinical and Translational Neurology|July 25, 2020
Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?Romina Moavero, Katarzyna Kotulska, Lieven Lagae, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Brain Communications|November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformationsSandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.
Annals of Neurology|November 12, 2020
Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP TrialKatarzyna Kotulska, David J Kwiatkowski, Paolo Curatolo, et al.
Neurology|January 25, 2022
Development and Validation of a Prediction Model for Early Diagnosis of <i>SCN1A</i>-Related EpilepsiesAndreas Brunklaus, Eduardo Pérez-Palma, Ismael Ghanty, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
Pageof 31