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Neuromuscular Disorders : NMD|June 1, 1997
From mutation to myotonia in sodium channel disordersS C CannonKidney International|March 18, 2000
Spectrum of sodium channel disturbances in the nondystrophic myotonias and periodic paralysesS C CannonNeuromuscular Disorders : NMD|July 16, 2002
An expanding view for the molecular basis of familial periodic paralysisStephen C CannonNeurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Physiologic principles underlying ion channelopathiesStephen C CannonThe Journal of Physiology|February 17, 2010
Voltage-sensor mutations in channelopathies of skeletal muscleStephen C CannonTrends in Neurosciences|January 1, 1996
Ion-channel defects and aberrant excitability in myotonia and periodic paralysisS C CannonComprehensive Physiology|April 17, 2015
Channelopathies of skeletal muscle excitabilityStephen C CannonThe Biochemical Journal|November 1, 1985
Electron transfer to nitrogenase in Klebsiella pneumoniae. nifF gene cloned and the gene product, a flavodoxin, purifiedJ Deistung, F C Cannon, M C Cannon, et al.Plos Computational Biology|August 29, 2006
The ion channel inverse problem: neuroinformatics meets biophysicsRobert C Cannon, Giampaolo D'AlessandroThe Journal of General Physiology|January 5, 1999
The position of the fast-inactivation gate during lidocaine block of voltage-gated Na+ channelsV Vedantham, S C CannonPageof 43