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Acute Medicine|May 26, 2011
Jaundice, renal failure and pulmonary haemorrhage in a canal boat ownerS Dawson, A Lind, C CannonMuscle & Nerve|November 28, 2007
Paradoxical depolarization of BA2+- treated muscle exposed to low extracellular K+: insights into resting potential abnormalities in hypokalemic paralysisArie F Struyk, Stephen C CannonThe Journal of General Physiology|August 30, 2000
COOH-terminal truncated alpha(1S) subunits conduct current better than full-length dihydropyridine receptorsJ A Morrill, S C CannonThe Journal of Physiology|July 1, 1993
Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysisS C Cannon, D P CoreyJournal of Biomechanical Engineering|August 1, 1983
Predictions of the existence, frequency, and amplitude of physiological tremor in normal man based on measured frequency-response characteristicsG I Zahalak, S C CannonNeuron|February 1, 1993
Functional expression of sodium channel mutations identified in families with periodic paralysisS C Cannon, S M StrittmatterJournal of Biomechanics|January 1, 1982
The mechanical behavior of active human skeletal muscle in small oscillationsS C Cannon, G I ZahalakThe Journal of Physiology|December 18, 2001
Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channelM P Takahashi, S C CannonThe Journal of General Physiology|October 3, 2002
Slow inactivation does not block the aqueous accessibility to the outer pore of voltage-gated Na channelsArie F Struyk, Stephen C CannonBiophysical Journal|February 4, 1999
Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotoniaM P Takahashi, S C CannonPageof 43