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Kimmo Kontula

Showing results (1-10 of 97) with videos related to

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Annals of Medicine|June 21, 2012
Clinical and molecular approaches to individualize antihypertensive drug therapyTimo P Hiltunen, Kimmo Kontula
European Journal of Human Genetics : EJHG|October 23, 2003
Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphismsPäivi J Laitinen, Heikki Swan, Kimmo Kontula
Journal of Cardiovascular Electrophysiology|February 22, 2005
Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutationsHeikki Swan, Päivi Laitinen, Kimmo Kontula, et al.
BMC Medical Genetics|January 20, 2011
KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?Annukka M Lahtinen, Annukka Marjamaa, Heikki Swan, et al.
Pacing and Clinical Electrophysiology : PACE|March 1, 2005
Effects of epinephrine on right ventricular monophasic action potentials in the LQT1 versus LQT2 form of long QT syndrome: preferential enhancement of "triangulation" in LQT1Matti Viitasalo, Kristian J Paavonen, Heikki Swan, et al.
Journal of the American Geriatrics Society|January 26, 2005
Genetic variant of lactase-persistent C/T-13910 is associated with bone fractures in very old ageNabil S Enattah, Raimo Sulkava, Pirjo Halonen, et al.
Journal of Cellular Physiology|January 25, 2002
Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardiaAndrew R Marks, Silvia Priori, Mirella Memmi, et al.
Heart Rhythm|October 22, 2008
U-waves and T-wave peak to T-wave end intervals in patients with catecholaminergic polymorphic ventricular tachycardia, effects of beta-blockersMatti Viitasalo, Lasse Oikarinen, Heikki Väänänen, et al.
Atherosclerosis|December 2, 2014
Prevalence and clinical correlates of familial hypercholesterolemia founder mutations in the general populationAnnukka M Lahtinen, Aki S Havulinna, Antti Jula, et al.
Heart Rhythm|May 1, 2007
Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointesAnnukka Lehtonen, Heidi Fodstad, Päivi Laitinen-Forsblom, et al.
Pageof 10

Showing results (1-10 of 97) with videos related to

Sort By:
Pageof 10
Annals of Medicine|June 21, 2012
Clinical and molecular approaches to individualize antihypertensive drug therapyTimo P Hiltunen, Kimmo Kontula
European Journal of Human Genetics : EJHG|October 23, 2003
Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphismsPäivi J Laitinen, Heikki Swan, Kimmo Kontula
Journal of Cardiovascular Electrophysiology|February 22, 2005
Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutationsHeikki Swan, Päivi Laitinen, Kimmo Kontula, et al.
BMC Medical Genetics|January 20, 2011
KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?Annukka M Lahtinen, Annukka Marjamaa, Heikki Swan, et al.
Pacing and Clinical Electrophysiology : PACE|March 1, 2005
Effects of epinephrine on right ventricular monophasic action potentials in the LQT1 versus LQT2 form of long QT syndrome: preferential enhancement of "triangulation" in LQT1Matti Viitasalo, Kristian J Paavonen, Heikki Swan, et al.
Journal of the American Geriatrics Society|January 26, 2005
Genetic variant of lactase-persistent C/T-13910 is associated with bone fractures in very old ageNabil S Enattah, Raimo Sulkava, Pirjo Halonen, et al.
Journal of Cellular Physiology|January 25, 2002
Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardiaAndrew R Marks, Silvia Priori, Mirella Memmi, et al.
Heart Rhythm|October 22, 2008
U-waves and T-wave peak to T-wave end intervals in patients with catecholaminergic polymorphic ventricular tachycardia, effects of beta-blockersMatti Viitasalo, Lasse Oikarinen, Heikki Väänänen, et al.
Atherosclerosis|December 2, 2014
Prevalence and clinical correlates of familial hypercholesterolemia founder mutations in the general populationAnnukka M Lahtinen, Aki S Havulinna, Antti Jula, et al.
Heart Rhythm|May 1, 2007
Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointesAnnukka Lehtonen, Heidi Fodstad, Päivi Laitinen-Forsblom, et al.
Pageof 10