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K Jurkat-Rott

Showing results (21-30 of 49) with videos related to

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Human Molecular Genetics|September 15, 1999
Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture testA Brandt, L Schleithoff, K Jurkat-Rott, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 8, 2008
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutationD I Zafeiriou, F Lehmann-Horn, E Vargiami, et al.
Neurology|September 18, 2007
Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutationsT V Wuttke, K Jurkat-Rott, W Paulus, et al.
The Journal of Physiology|March 1, 1995
Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubesI Sipos, K Jurkat-Rott, C Harasztosi, et al.
Advances in Medical Sciences|January 31, 2008
Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutationA Winczewska-Wiktor, B Steinborn, F Lehman-Horn, et al.
Neurology|August 26, 2006
Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weaknessM-A Weber, S Nielles-Vallespin, M Essig, et al.
FEBS Letters|March 25, 1998
Calcium currents and transients of native and heterologously expressed mutant skeletal muscle DHP receptor alpha1 subunits (R528H)K Jurkat-Rott, U Uetz, U Pika-Hartlaub, et al.
Society of General Physiologists Series|January 1, 1995
Altered calcium currents in human hypokalemic periodic paralysis myotubes expressing mutant L-type calcium channelsF Lehmann-Horn, I Sipos, K Jurkat-Rott, et al.
British Journal of Anaesthesia|November 30, 2000
Xenon does not induce contracture in human malignant hyperthermia muscleC P Baur, W Klingler, K Jurkat-Rott, et al.
Journal of Neurology|May 1, 2012
Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degenerationM-A Weber, A M Nagel, M B Wolf, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|September 15, 1999
Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture testA Brandt, L Schleithoff, K Jurkat-Rott, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 8, 2008
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutationD I Zafeiriou, F Lehmann-Horn, E Vargiami, et al.
Neurology|September 18, 2007
Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutationsT V Wuttke, K Jurkat-Rott, W Paulus, et al.
The Journal of Physiology|March 1, 1995
Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubesI Sipos, K Jurkat-Rott, C Harasztosi, et al.
Advances in Medical Sciences|January 31, 2008
Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutationA Winczewska-Wiktor, B Steinborn, F Lehman-Horn, et al.
Neurology|August 26, 2006
Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weaknessM-A Weber, S Nielles-Vallespin, M Essig, et al.
FEBS Letters|March 25, 1998
Calcium currents and transients of native and heterologously expressed mutant skeletal muscle DHP receptor alpha1 subunits (R528H)K Jurkat-Rott, U Uetz, U Pika-Hartlaub, et al.
Society of General Physiologists Series|January 1, 1995
Altered calcium currents in human hypokalemic periodic paralysis myotubes expressing mutant L-type calcium channelsF Lehmann-Horn, I Sipos, K Jurkat-Rott, et al.
British Journal of Anaesthesia|November 30, 2000
Xenon does not induce contracture in human malignant hyperthermia muscleC P Baur, W Klingler, K Jurkat-Rott, et al.
Journal of Neurology|May 1, 2012
Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degenerationM-A Weber, A M Nagel, M B Wolf, et al.
Pageof 5