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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 4, 2007
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsionsMaria Virginia Soldovieri, Maria Roberta Cilio, Francesco Miceli, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 14, 2014
The endocannabinoid 2-AG controls skeletal muscle cell differentiation via CB1 receptor-dependent inhibition of Kv7 channelsFabio A Iannotti, Cristoforo Silvestri, Enrico Mazzarella, et al.
EMBO Molecular Medicine|June 27, 2023
Targeting shared molecular etiologies to accelerate drug development for rare diseasesGalliano Zanello, Macarena Garrido-Estepa, Ana Crespo, et al.
Epilepsia|November 27, 2016
Rapid and safe response to low-dose carbamazepine in neonatal epilepsyTristan T Sands, Martina Balestri, Giulia Bellini, et al.
Molecular and Cellular Neurosciences|January 20, 2016
Characterization of two de novoKCNT1 mutations in children with malignant migrating partial seizures in infancyFrancesca Rizzo, Paolo Ambrosino, Anna Guacci, et al.
Biochimica Et Biophysica Acta|June 16, 2015
Epilepsy-causing mutations in Kv7.2 C-terminus affect binding and functional modulation by calmodulinPaolo Ambrosino, Alessandro Alaimo, Silvia Bartollino, et al.
Annals of Neurology|May 10, 2018
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathyPaolo Ambrosino, Maria Virginia Soldovieri, Thomas Bast, et al.
Epilepsia|November 19, 2016
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variantJohn J Millichap, Francesco Miceli, Michela De Maria, et al.
Annals of Neurology|February 21, 2025
Fluoxetine Treatment in Epilepsy of Infancy with Migrating Focal Seizures Due to KCNT1 Variants: An Open Label StudyMarina Trivisano, Ilaria Mosca, Licia Salimbene, et al.
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