Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Rima Nabbout

Showing results (131-140 of 310) with videos related to

Pageof 31
Sort By:
Pediatric Neurology|February 11, 2023
Review of Machine Learning and Artificial Intelligence (ML/AI) for the Pediatric NeurologistGrace Y Gombolay, Nakul Gopalan, Andrea Bernasconi, et al.
Epilepsia|February 28, 2006
Epilepsy in Menkes disease: analysis of clinical stagesNadia Bahi-Buisson, Anna Kaminska, Rima Nabbout, et al.
Orphanet Journal of Rare Diseases|November 15, 2013
Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsyRima Nabbout, Nicole Chemaly, Mathilde Chipaux, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|December 10, 2025
Quantitative EEG enhances early assessment and prognostic stratification of brain dysfunction in infants with abusive head traumaValentin Hess, Matthieu Doyen, Rima Nabbout, et al.
Epilepsy & Behavior : E&B|November 7, 2020
Attachment insecurity in infants with infantile spasms: Maternal anxiety and sadness, and infant's temperament outweigh disease severityLaure Boissel, Guillaume Le Borgne, Luisa Fuentealba Baldini, et al.
Neurosurgery|April 13, 2026
Microsurgical Resection of Subependymal Giant Cell Astrocytoma: Single-Center Retrospective Analysis and Meta-AnalysisLuca Sartori, Lelio Guida, Stéphanie Puget, et al.
Epilepsia Open|March 15, 2019
Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotypeLisa Ouss, Dorothee Leunen, Jacques Laschet, et al.
Orphanet Journal of Rare Diseases|March 2, 2024
Istore: a project on innovative statistical methodologies to improve rare diseases clinical trials in limited populationsStefanie Schoenen, Johan Verbeeck, Lukas Koletzko, et al.
Developmental Medicine and Child Neurology|November 12, 2025
Intravenous immunoglobulin and febrile status epilepticus in children with Dravet syndrome: A retrospective multicentre studyRomane Marc, Nicole Chemaly, Mathieu Kuchenbuch, et al.
Human Mutation|March 26, 2013
Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancyMathieu Milh, Antonio Falace, Nathalie Villeneuve, et al.
Pageof 31

Showing results (131-140 of 310) with videos related to

Sort By:
Pageof 31
Pediatric Neurology|February 11, 2023
Review of Machine Learning and Artificial Intelligence (ML/AI) for the Pediatric NeurologistGrace Y Gombolay, Nakul Gopalan, Andrea Bernasconi, et al.
Epilepsia|February 28, 2006
Epilepsy in Menkes disease: analysis of clinical stagesNadia Bahi-Buisson, Anna Kaminska, Rima Nabbout, et al.
Orphanet Journal of Rare Diseases|November 15, 2013
Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsyRima Nabbout, Nicole Chemaly, Mathilde Chipaux, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|December 10, 2025
Quantitative EEG enhances early assessment and prognostic stratification of brain dysfunction in infants with abusive head traumaValentin Hess, Matthieu Doyen, Rima Nabbout, et al.
Epilepsy & Behavior : E&B|November 7, 2020
Attachment insecurity in infants with infantile spasms: Maternal anxiety and sadness, and infant's temperament outweigh disease severityLaure Boissel, Guillaume Le Borgne, Luisa Fuentealba Baldini, et al.
Neurosurgery|April 13, 2026
Microsurgical Resection of Subependymal Giant Cell Astrocytoma: Single-Center Retrospective Analysis and Meta-AnalysisLuca Sartori, Lelio Guida, Stéphanie Puget, et al.
Epilepsia Open|March 15, 2019
Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotypeLisa Ouss, Dorothee Leunen, Jacques Laschet, et al.
Orphanet Journal of Rare Diseases|March 2, 2024
Istore: a project on innovative statistical methodologies to improve rare diseases clinical trials in limited populationsStefanie Schoenen, Johan Verbeeck, Lukas Koletzko, et al.
Developmental Medicine and Child Neurology|November 12, 2025
Intravenous immunoglobulin and febrile status epilepticus in children with Dravet syndrome: A retrospective multicentre studyRomane Marc, Nicole Chemaly, Mathieu Kuchenbuch, et al.
Human Mutation|March 26, 2013
Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancyMathieu Milh, Antonio Falace, Nathalie Villeneuve, et al.
Pageof 31