Showing results (11-20 of 212) with videos related to
Sort By:
Pageof 22
Acta Anaesthesiologica Scandinavica|May 1, 1991
Characterization of swine susceptible to malignant hyperthermia by in vivo, in vitro and post-mortem techniquesM J Seewald, H M Eichinger, F Lehmann-Horn, et al.Muscle & Nerve|June 1, 1990
Schwartz-Jampel syndrome: II. Na+ channel defect causes myotoniaF Lehmann-Horn, P A Iaizzo, C Franke, et al.Muscle & Nerve|March 1, 1989
Malignant hyperthermia: effects of halothane on the surface membraneP A Iaizzo, F Lehmann-Horn, S R Taylor, et al.The Journal of Physiology|November 14, 1997
Chloride conductance in mouse muscle is subject to post-transcriptional compensation of the functional Cl- channel 1 gene dosageM F Chen, R Niggeweg, P A Iaizzo, et al.Muscle & Nerve|August 1, 1991
Altered Na+ channel activity and reduced Cl- conductance cause hyperexcitability in recessive generalized myotonia (Becker)C Franke, P A Iaizzo, H Hatt, et al.British Journal of Anaesthesia|March 4, 2000
Malignant hyperthermia causing Gly2435Arg mutation of the ryanodine receptor facilitates ryanodine-induced calcium release in myotubesH Brinkmeier, J Krämer, R Krämer, et al.Neuromuscular Disorders : NMD|January 1, 1991
Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenitaP A Iaizzo, C Franke, H Hatt, et al.Neuromuscular Disorders : NMD|January 1, 1992
Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutationsT Deufel, W Müller-Felber, D E Pongratz, et al.Current Opinion in Neurology|October 1, 1995
Hereditary nondystrophic myotonias and periodic paralysesF Lehmann-Horn, R RüdelSeminars in Pediatric Neurology|June 1, 1996
Channelopathies: the nondystrophic myotonias and periodic paralysesF Lehmann-Horn, R RüdelPageof 22