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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.Human Molecular Genetics|July 1, 1994
Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletionR Heine, A L George, U Pika, et al.Neurology|October 27, 1997
A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivityS Wagner, H Lerche, N Mitrovic, et al.Muscle & Nerve|February 1, 1983
Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parametersF Lehmann-Horn, R Rüdel, K Ricker, et al.Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|June 9, 1998
[A remote access system for inquiry of centrally stored data on patients suspected of malignant hyperthermia . A prototypical development for the Internet]C Baur, M Kranawetter, S Weiss-Kubat, et al.Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.Genomics|July 1, 1991
Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19K Kausch, F Lehmann-Horn, M Janka, et al.Muscle & Nerve|September 15, 1998
Transient weakness and compound muscle action potential decrement in myotonia congenitaF Deymeer, S Cakirkaya, P Serdaroğlu, et al.European Biophysics Journal : EBJ|December 14, 1999
On identification of Na(+) channel gating schemes using moving-average filtered hidden Markov modelsS Michalek, H Lerche, M Wagner, et al.Muscle & Nerve|January 12, 1999
Electrical myotonia in heterozygous carriers of recessive myotonia congenitaF Deymeer, F Lehmann-Horn, P Serdaroğlu, et al.Pageof 56