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Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.Proceedings of the National Academy of Sciences of the United States of America|August 16, 2000
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced currentK Jurkat-Rott, N Mitrovic, C Hang, et al.Annals of Neurology|September 11, 1999
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsionsH Lerche, C Biervert, A K Alekov, et al.Neurology|March 12, 2010
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2Y G Weber, R Roebling, J Kassubek, 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.Neurology|July 8, 2011
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxiasM Strupp, R Kalla, J Claassen, et al.Current Opinion in Neurology|October 1, 1995
Hereditary nondystrophic myotonias and periodic paralysesF Lehmann-Horn, R RüdelSeminars in Pediatric Neurology|June 1, 1996
Channelopathies: the nondystrophic myotonias and periodic paralysesF Lehmann-Horn, R RüdelAnesthesia and Analgesia|January 7, 2000
A multicenter study of 4-chloro-m-cresol for diagnosing malignant hyperthermia susceptibilityC P Baur, L Bellon, P Felleiter, et al.Muscle & Nerve|March 1, 1990
The correlation between electrical after-activity and slowed relaxation in myotoniaP A Iaizzo, F Lehmann-HornPageof 56