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Molecular Pain|December 6, 2011
Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7Mark Estacion, Chongyang Han, Jin-Sung Choi, et al.
Annals of Neurology|June 24, 2011
Gain of function Naν1.7 mutations in idiopathic small fiber neuropathyCatharina G Faber, Janneke G J Hoeijmakers, Hye-Sook Ahn, et al.
Brain : a Journal of Neurology|February 4, 2020
Differential effect of lacosamide on Nav1.7 variants from responsive and non-responsive patients with small fibre neuropathyJulie I R Labau, Mark Estacion, Brian S Tanaka, et al.
Epilepsy Research|September 21, 2014
Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathyCarolien G F de Kovel, Miriam H Meisler, Eva H Brilstra, et al.
Biorxiv : the Preprint Server for Biology|September 18, 2025
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
Cell|March 12, 2026
Human-specific features of the cerebellum and ZP2-regulated synapse developmentSuel-Kee Kim, Adriana Cherskov, Aastha Sindhwani, et al.
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