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Karin Jurkat-Rott

Showing results (21-30 of 82) with videos related to

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Pflugers Archiv : European Journal of Physiology|March 3, 2007
Gating of the HypoPP-1 mutations: II. Effects of a calcium-channel agonist BayK 8644Alexey Kuzmenkin, Chao Hang, Elza Kuzmenkina, et al.
Channels (Austin, Tex.)|December 9, 2014
Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutationJames R Groome, Karin Jurkat-Rott, Frank Lehmann-Horn
Advances in Experimental Medicine and Biology|September 9, 2010
Hereditary channelopathies in neurologyKarin Jurkat-Rott, Holger Lerche, Yvonne Weber, et al.
Pflugers Archiv : European Journal of Physiology|March 19, 2010
Sodium channelopathies of skeletal muscle result from gain or loss of functionKarin Jurkat-Rott, Boris Holzherr, Michael Fauler, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 28, 2017
Successful treatment of periodic paralysis with coenzyme Q10: two case reportsYuwei Da, Lin Lei, Karin Jurkat-Rott, et al.
Pflugers Archiv : European Journal of Physiology|August 5, 2003
Impaired slow inactivation due to a polymorphism and substitutions of Ser-906 in the II-III loop of the human Nav1.4 channelAlexey Kuzmenkin, Karin Jurkat-Rott, Frank Lehmann-Horn, et al.
Studies in Health Technology and Informatics|May 15, 2014
Towards the automated generation of expert profiles for rare diseases through bibliometric analysisAndreas Pflugrad, Karin Jurkat-Rott, Frank Lehmann-Horn, et al.
Pediatric Neurology|July 9, 2013
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraineIciar Sánchez-Albisua, Martin Schöning, Karin Jurkat-Rott, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
The role of fibrosis in Duchenne muscular dystrophyWerner Klingler, Karin Jurkat-Rott, Frank Lehmann-Horn, et al.
Cephalalgia : an International Journal of Headache|November 18, 2017
Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499LVictoria Schubert, Eva Auffenberg, Saskia Biskup, et al.
Pageof 9

Showing results (21-30 of 82) with videos related to

Sort By:
Pageof 9
Pflugers Archiv : European Journal of Physiology|March 3, 2007
Gating of the HypoPP-1 mutations: II. Effects of a calcium-channel agonist BayK 8644Alexey Kuzmenkin, Chao Hang, Elza Kuzmenkina, et al.
Channels (Austin, Tex.)|December 9, 2014
Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutationJames R Groome, Karin Jurkat-Rott, Frank Lehmann-Horn
Advances in Experimental Medicine and Biology|September 9, 2010
Hereditary channelopathies in neurologyKarin Jurkat-Rott, Holger Lerche, Yvonne Weber, et al.
Pflugers Archiv : European Journal of Physiology|March 19, 2010
Sodium channelopathies of skeletal muscle result from gain or loss of functionKarin Jurkat-Rott, Boris Holzherr, Michael Fauler, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 28, 2017
Successful treatment of periodic paralysis with coenzyme Q10: two case reportsYuwei Da, Lin Lei, Karin Jurkat-Rott, et al.
Pflugers Archiv : European Journal of Physiology|August 5, 2003
Impaired slow inactivation due to a polymorphism and substitutions of Ser-906 in the II-III loop of the human Nav1.4 channelAlexey Kuzmenkin, Karin Jurkat-Rott, Frank Lehmann-Horn, et al.
Studies in Health Technology and Informatics|May 15, 2014
Towards the automated generation of expert profiles for rare diseases through bibliometric analysisAndreas Pflugrad, Karin Jurkat-Rott, Frank Lehmann-Horn, et al.
Pediatric Neurology|July 9, 2013
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraineIciar Sánchez-Albisua, Martin Schöning, Karin Jurkat-Rott, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
The role of fibrosis in Duchenne muscular dystrophyWerner Klingler, Karin Jurkat-Rott, Frank Lehmann-Horn, et al.
Cephalalgia : an International Journal of Headache|November 18, 2017
Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499LVictoria Schubert, Eva Auffenberg, Saskia Biskup, et al.
Pageof 9