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Brain : a Journal of Neurology|June 5, 2026
Kv7.2 loss-of-function causes early hyperexcitability and network remodellingNina Dirkx, Marcus Kaji, Els De Vriendt, et al.Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|August 17, 2018
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized TherapyRobertino Dilena, Jacopo C DiFrancesco, Maria Virginia Soldovieri, et al.Journal of Medicinal Chemistry|August 16, 2022
Beyond Retigabine: Design, Synthesis, and Pharmacological Characterization of a Potent and Chemically Stable Neuronal Kv7 Channel Activator with Anticonvulsant ActivitySimona Musella, Lidia Carotenuto, Nunzio Iraci, et al.Human Mutation|December 31, 2013
Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1AMaria Virginia Soldovieri, Nadia Boutry-Kryza, Mathieu Milh, et al.Journal of Medicinal Chemistry|May 23, 2024
In Silico Assisted Identification, Synthesis, and In Vitro Pharmacological Characterization of Potent and Selective Blockers of the Epilepsy-Associated KCNT1 ChannelNunzio Iraci, Lidia Carotenuto, Tania Ciaglia, et al.Journal of Medicinal Chemistry|December 10, 2019
Synthesis and Pharmacological Characterization of Conformationally Restricted Retigabine Analogues as Novel Neuronal Kv7 Channel ActivatorsCarmine Ostacolo, Francesco Miceli, Veronica Di Sarno, et al.Aging Clinical and Experimental Research|September 1, 2020
Cytokine storm in aged people with CoV-2: possible role of vitamins as therapy or preventive strategySirio Fiorino, Claudio Gallo, Maddalena Zippi, et al.Ebiomedicine|July 3, 2022
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanismFrancesco Miceli, Charissa Millevert, Maria Virginia Soldovieri, 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.Annals of Neurology|June 10, 2019
Autism and developmental disability caused by KCNQ3 gain-of-function variantsTristan T Sands, Francesco Miceli, Gaetan Lesca, et al.Pageof 6