Showing results (81-90 of 557) with videos related to
Sort By:
Pageof 56
European Journal of Pharmacology|September 4, 1990
K+ channel openers suppress myotonic activity of human skeletal muscle in vitroS Quasthoff, A Spuler, W Spittelmeister, et al.Pflugers Archiv : European Journal of Physiology|January 1, 1996
Expression and functional characterization of the cardiac L-type calcium channel carrying a skeletal muscle DHP-receptor mutation causing hypokalaemic periodic paralysisH Lerche, N Klugbauer, F Lehmann-Horn, et al.Cell Calcium|April 1, 1989
The use of Fura-2 to estimate myoplasmic [Ca2+] in human skeletal muscleP A Iaizzo, M Seewald, S G Oakes, et al.Pflugers Archiv : European Journal of Physiology|August 26, 1998
Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenitaR Fleischhauer, N Mitrovic, F Deymeer, et al.Anaesthesia|June 10, 2014
Contractile elements in muscular fascial tissue - implications for in-vitro contracture testing for malignant hyperthermiaK Hoppe, R Schleip, F Lehmann-Horn, et al.Muscle & Nerve|September 1, 1985
In vivo P-NMR spectroscopy: muscle energy exchange in paramyotonia patientsF Lehmann-Horn, D Höpfel, R Rüdel, et al.Human Genetics|November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)E Plassart, A Elbaz, J V Santos, et al.Nature Genetics|March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European familiesB Fontaine, J Vale-Santos, K Jurkat-Rott, et al.Muscle & Nerve|November 1, 1989
Adynamia episodica hereditaria: what causes the weakness?K Ricker, L M Camacho, P Grafe, et al.The Journal of Biological Chemistry|February 21, 1997
Functional characterization of a distinct ryanodine receptor mutation in human malignant hyperthermia-susceptible muscleM Richter, L Schleithoff, T Deufel, et al.Pageof 56