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Karin Jurkat-Rott

Showing results (61-70 of 82) with videos related to

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Radiology|February 6, 2014
In vivo 35Cl MR imaging in humans: a feasibility studyArmin M Nagel, Frank Lehmann-Horn, Marc-André Weber, et al.
Human Genetics|January 11, 2003
Several interacting genes influence the malignant hyperthermia phenotypeRachel Robinson, Philip Hopkins, Antonella Carsana, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2009
K+-dependent paradoxical membrane depolarization and Na+ overload, major and reversible contributors to weakness by ion channel leaksKarin Jurkat-Rott, Marc-André Weber, Michael Fauler, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 19, 2018
Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of lifeFrank Lehmann-Horn, Adele D'Amico, Enrico Bertini, et al.
JAMA Neurology|September 25, 2013
Hypokalemic periodic paralysis induced by thymic hyperplasia and relieved by thymectomyRenrong Yang, Karin Jurkat-Rott, Jinlin Cao, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Neuromuscular Disorders : NMD|October 24, 2015
Divalent cation-responsive myotonia and muscle paralysis in skeletal muscle sodium channelopathyAmi Mankodi, Christopher Grunseich, Martin Skov, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
<sup>23</sup>Na MRI and myometry to compare eplerenone vs. glucocorticoid treatment in Duchenne dystrophyPhilip A Glemser, Heike Jaeger, Armin M Nagel, et al.
Neuromuscular Disorders : NMD|December 28, 2016
A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotypeMarcin Bednarz, Bas C Stunnenberg, Benno Kusters, et al.
Human Mutation|August 20, 2005
Rare missense variants in ATP1A2 in families with clustering of common forms of migraineUnda Todt, Martin Dichgans, Karin Jurkat-Rott, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Radiology|February 6, 2014
In vivo 35Cl MR imaging in humans: a feasibility studyArmin M Nagel, Frank Lehmann-Horn, Marc-André Weber, et al.
Human Genetics|January 11, 2003
Several interacting genes influence the malignant hyperthermia phenotypeRachel Robinson, Philip Hopkins, Antonella Carsana, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2009
K+-dependent paradoxical membrane depolarization and Na+ overload, major and reversible contributors to weakness by ion channel leaksKarin Jurkat-Rott, Marc-André Weber, Michael Fauler, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 19, 2018
Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of lifeFrank Lehmann-Horn, Adele D'Amico, Enrico Bertini, et al.
JAMA Neurology|September 25, 2013
Hypokalemic periodic paralysis induced by thymic hyperplasia and relieved by thymectomyRenrong Yang, Karin Jurkat-Rott, Jinlin Cao, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Neuromuscular Disorders : NMD|October 24, 2015
Divalent cation-responsive myotonia and muscle paralysis in skeletal muscle sodium channelopathyAmi Mankodi, Christopher Grunseich, Martin Skov, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
<sup>23</sup>Na MRI and myometry to compare eplerenone vs. glucocorticoid treatment in Duchenne dystrophyPhilip A Glemser, Heike Jaeger, Armin M Nagel, et al.
Neuromuscular Disorders : NMD|December 28, 2016
A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotypeMarcin Bednarz, Bas C Stunnenberg, Benno Kusters, et al.
Human Mutation|August 20, 2005
Rare missense variants in ATP1A2 in families with clustering of common forms of migraineUnda Todt, Martin Dichgans, Karin Jurkat-Rott, et al.
Pageof 9