Showing results (101-110 of 131) with videos related to

Sort By:
Pageof 14
Medical Hypotheses|October 8, 2005
Passive muscle stiffness may be influenced by active contractility of intramuscular connective tissueRobert Schleip, Ian L Naylor, Daniel Ursu, et al.
Brain : a Journal of Neurology|November 19, 2013
Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutationChunxiang Fan, Frank Lehmann-Horn, Marc-André Weber, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 11, 2005
3,4-Methylenedioxymethamphetamine (ecstasy) activates skeletal muscle nicotinic acetylcholine receptorsWerner Klingler, James J A Heffron, Karin Jurkat-Rott, et al.
The Journal of Physiology|May 30, 2012
Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenitaSebastian Weinberger, Daniel Wojciechowski, Damien Sternberg, et al.
Muscle & Nerve|June 26, 2007
Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutationThomas Meyer, Karin Jurkat-Rott, Angela Huebner, et al.
Frontiers in Physiology|December 17, 2020
Paxilline Prevents the Onset of Myotonic Stiffness in Pharmacologically Induced Myotonia: A Preclinical InvestigationKerstin Hoppe, Tina Sartorius, Sunisa Chaiklieng, et al.
Neuropediatrics|June 22, 2019
Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 MutationVincent Zimmern, Florence Riant, Emmanuel Roze, et al.
Molecular Pharmacology|February 24, 2004
An apamin- and scyllatoxin-insensitive isoform of the human SK3 channelOliver H Wittekindt, Violeta Visan, Hiroaki Tomita, et al.
Cephalalgia : an International Journal of Headache|January 15, 2016
Early-onset familial hemiplegic migraine due to a novel SCN1A mutationChunxiang Fan, Stefan Wolking, Frank Lehmann-Horn, et al.
Radiology|February 6, 2014
In vivo 35Cl MR imaging in humans: a feasibility studyArmin M Nagel, Frank Lehmann-Horn, Marc-André Weber, et al.
Pageof 14