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Annals of Neurology|May 1, 1996
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscleH Lerche, N Mitrovic, V Dubowitz, et al.Acta Neurologica Scandinavica|January 6, 2010
Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenitaC Kornblum, G G Lutterbey, B Czermin, et al.The Journal of Physiology|June 1, 1990
Characteristics of Na+ channels and Cl- conductance in resealed muscle fibre segments from patients with myotonic dystrophyC Franke, H Hatt, P A Iaizzo, et al.The Biochemical Journal|May 15, 1995
Activation and labelling of the purified skeletal muscle ryanodine receptor by an oxidized ATP analogueM Hohenegger, A Herrmann-Frank, M Richter, et al.Pflugers Archiv : European Journal of Physiology|April 1, 1991
Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysisF Lehmann-Horn, P A Iaizzo, H Hatt, et al.Pflugers Archiv : European Journal of Physiology|March 1, 1995
Characterization of the high-conductance Ca(2+)-activated K+ channel in adult human skeletal muscleH Lerche, C Fahlke, P A Iaizzo, et al.Human Molecular Genetics|August 1, 1995
Myotonia levior is a chloride channel disorderF Lehmann-Horn, V Mailänder, R Heine, et al.Archives of Neurology|November 1, 1994
Myotonia fluctuans. A third type of muscle sodium channel diseaseK Ricker, R T Moxley, R Heine, et al.Neurology|October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variationN P Davies, P Imbrici, D Fialho, et al.The Journal of Physiology|June 22, 1999
A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMKW Peter, N Mitrovic, M Schiebe, et al.Pageof 56