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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.Pflugers Archiv : European Journal of Physiology|June 17, 1999
A transient and a persistent calcium release are induced by chlorocresol in cultivated mouse myotubesM H Gschwend, R Rüdel, H Brinkmeier, 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.Journal of the Neurological Sciences|January 6, 2000
The small sodium-channel blocking factor in the cerebrospinal fluid of multiple sclerosis patients is probably an oligopeptideP Aulkemeyer, G Hausner, H Brinkmeier, 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.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.Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 9, 2002
Optical detection of mitochondrial NADH content in intact human myotubesM H Gschwend, R Rüdel, W S Strauss, 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.Muscle & Nerve|January 12, 1999
Electrical myotonia in heterozygous carriers of recessive myotonia congenitaF Deymeer, F Lehmann-Horn, P Serdaroğlu, et al.Muscle & Nerve|July 1, 1995
Cerebrospinal fluid and serum from patients with inflammatory polyradiculoneuropathy have opposite effects on sodium channelsA Würz, H Brinkmeier, K H Wollinsky, et al.Pageof 12