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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.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
The European Journal of Neuroscience|June 26, 2001
Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in manA K Alekov, M M Rahman, N Mitrovic, et al.
Muscle & Nerve|September 1, 1981
Membrane defects in paramyotonia congenita with and without myotonia in a warm environmentF Lehmann-Horn, R Rüdel, R Dengler, et al.
Clinical Genetics|March 1, 1990
A linkage study of malignant hyperthermia (MH)K Bender, H Senff, T F Wienker, et al.
Muscle & Nerve|May 1, 1987
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pHF Lehmann-Horn, G Küther, K Ricker, 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.
EEG-EMG Zeitschrift Fur Elektroenzephalographie, Elektromyographie Und Verwandte Gebiete|December 1, 1991
[Visual evoked potentials in Alzheimer's and Parkinson disease]R Zimmer, H Walther, A Kurz, et al.
The Journal of Physiology|August 15, 1995
Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channelN Mitrović, A L George, H Lerche, et al.
Proceedings. Biological Sciences|April 2, 2010
Recovery of mechano-electrical transduction in rat cochlear hair bundles after postnatal destruction of the stereociliar cross-linksJ Ebert, S Fink, A Koitschev, et al.
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