Showing results (241-250 of 256) with videos related to

Sort By:
Pageof 26
Cerebellum (London, England)|February 26, 2022
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar DevelopmentAndrea Accogli, Shenzhao Lu, Ilaria Musante, et al.
Neurology. Genetics|March 4, 2021
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variantsFederica Malerba, Giulio Alberini, Ganna Balagura, et al.
Epilepsia|March 24, 2025
Expanding the therapeutic role of highly purified cannabidiol in monogenic epilepsies: A multicenter real-world studyEmanuele Cerulli Irelli, Adolfo Mazzeo, Roberto H Caraballo, et al.
Epilepsia|October 29, 2025
Lennox-Gastaut syndrome unveiled: Advancing diagnosis, therapies, and advocacy-insights from the Genoa International WorkshopAntonella Riva, Gianluca D'Onofrio, Elisabetta Amadori, et al.
Annals of Neurology|November 15, 2024
Automated and Interpretable Detection of Hippocampal Sclerosis in Temporal Lobe Epilepsy: AID-HSMathilde Ripart, Jordan DeKraker, Maria H Eriksson, et al.
Human Genetics|May 14, 2023
Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorderGianluca D'Onofrio, Andrea Accogli, Mariasavina Severino, et al.
Neurology. Genetics|June 3, 2022
Epilepsy Course and Developmental Trajectories in STXBP1-DEEGanna Balagura, Julie Xian, Antonella Riva, et al.
Brain : a Journal of Neurology|March 8, 2024
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disordersJai Sidpra, Sniya Sudhakar, Asthik Biswas, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy studyRebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Epilepsia|July 2, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variantsClaudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga, et al.
Pageof 26