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K Jurkat-Rott

Showing results (11-20 of 49) with videos related to

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Journal of Neurology|October 20, 1999
Teaching course: ion channelopathies in neurologyK Jurkat-Rott, H Lerche, N Mitrovic, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
A novel N440K sodium channel mutation causes myotonia with exercise-induced weakness--exclusion of CLCN1 exon deletion/duplication by MLPAF Lehmann-Horn, M Orth, M Kuhn, et al.
Neurology|November 24, 2004
SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamideS L Venance, K Jurkat-Rott, F Lehmann-Horn, et al.
Neurology|November 26, 2011
Sodium (23Na) MRI detects elevated muscular sodium concentration in Duchenne muscular dystrophyM-A Weber, A M Nagel, K Jurkat-Rott, et al.
The Journal of Clinical Investigation|March 13, 1999
Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysisD Tricarico, S Servidei, P Tonali, et al.
Journal of Neurology|July 26, 2013
Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individualsG Charles, C Zheng, F Lehmann-Horn, et al.
Clinical Genetics|October 8, 2016
Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na<sub>v</sub> 1.4 cause periodic paralysisC Fan, N Mao, F Lehmann-Horn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 15, 1998
Familial cramp due to potassium-aggravated myotoniaR W Orrell, K Jurkat-Rott, F Lehmann-Horn, et al.
Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|February 28, 2002
[Anesthesia in neuromuscular disorders. Part 1: introduction]C P Baur, R Schlecht, K Jurkat-Rott, et al.
Acta Anaesthesiologica Scandinavica|May 4, 2013
In vitro muscle contracture investigations on the malignant hyperthermia like episodes in myotonia congenitaK Hoppe, F Lehmann-Horn, S Chaiklieng, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Journal of Neurology|October 20, 1999
Teaching course: ion channelopathies in neurologyK Jurkat-Rott, H Lerche, N Mitrovic, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
A novel N440K sodium channel mutation causes myotonia with exercise-induced weakness--exclusion of CLCN1 exon deletion/duplication by MLPAF Lehmann-Horn, M Orth, M Kuhn, et al.
Neurology|November 24, 2004
SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamideS L Venance, K Jurkat-Rott, F Lehmann-Horn, et al.
Neurology|November 26, 2011
Sodium (23Na) MRI detects elevated muscular sodium concentration in Duchenne muscular dystrophyM-A Weber, A M Nagel, K Jurkat-Rott, et al.
The Journal of Clinical Investigation|March 13, 1999
Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysisD Tricarico, S Servidei, P Tonali, et al.
Journal of Neurology|July 26, 2013
Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individualsG Charles, C Zheng, F Lehmann-Horn, et al.
Clinical Genetics|October 8, 2016
Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na<sub>v</sub> 1.4 cause periodic paralysisC Fan, N Mao, F Lehmann-Horn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 15, 1998
Familial cramp due to potassium-aggravated myotoniaR W Orrell, K Jurkat-Rott, F Lehmann-Horn, et al.
Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|February 28, 2002
[Anesthesia in neuromuscular disorders. Part 1: introduction]C P Baur, R Schlecht, K Jurkat-Rott, et al.
Acta Anaesthesiologica Scandinavica|May 4, 2013
In vitro muscle contracture investigations on the malignant hyperthermia like episodes in myotonia congenitaK Hoppe, F Lehmann-Horn, S Chaiklieng, et al.
Pageof 5