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The European Journal of Neuroscience|June 26, 1999
Expression in mammalian cells and electrophysiological characterization of two mutant Kv1.1 channels causing episodic ataxia type 1 (EA-1)F Bretschneider, A Wrisch, F Lehmann-Horn, et al.Electromyography and Clinical Neurophysiology|July 1, 1992
Analysis of multiple EMG and acceleration signals of various record lengths as a means to study pathological and physiological oscillationsP A Iaizzo, R S PozosJournal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 1991
Shivering and pathological and physiological clonic oscillations of the human ankleR S Pozos, P A IaizzoAmerican Journal of Human Genetics|February 1, 1996
Novel muscle chloride channel mutations and their effects on heterozygous carriersV Mailänder, R Heine, F Deymeer, et al.Muscle & Nerve|May 1, 1990
Enhancement of K+ conductance improves in vitro the contraction force of skeletal muscle in hypokalemic periodic paralysisP Grafe, S Quasthoff, M Strupp, et al.Genomics|October 27, 1999
Genomic structure and functional expression of a human alpha(2)/delta calcium channel subunit gene (CACNA2)L Schleithoff, G Mehrke, B Reutlinger, et al.Muscle & Nerve|May 1, 1986
Muscle stiffness and electrical activity in paramyotonia congenitaK Ricker, R Rüdel, F Lehmann-Horn, et al.Muscle & Nerve|February 1, 1984
Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane parametersR Rüdel, F Lehmann-Horn, K Ricker, et al.Biophysical Journal|May 8, 1999
External tetraethylammonium as a molecular caliper for sensing the shape of the outer vestibule of potassium channelsF Bretschneider, A Wrisch, F Lehmann-Horn, et al.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.Pageof 22