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Kimmo Kontula

Showing results (11-20 of 97) with videos related to

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International Journal of Cardiology|September 29, 2009
Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitroAnnukka Marjamaa, Päivi Laitinen-Forsblom, Anetta Wronska, et al.
Cardiovascular Research|May 26, 2005
Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insightsKimmo Kontula, Päivi J Laitinen, Annukka Lehtonen, et al.
European Journal of Endocrinology|October 19, 2012
Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1Kati M Donner, Timo P Hiltunen, Olli A Jänne, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|October 14, 2011
STK39 variation predicts the ambulatory blood pressure response to losartan in hypertensive menKati M Donner, Timo P Hiltunen, Tuula Hannila-Handelberg, et al.
International Journal of Legal Medicine|April 12, 2003
Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in waterPhilippe Lunetta, Antti Levo, Päivi J Laitinen, et al.
Annals of Medicine|June 5, 2004
Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardiaPäivi J Laitinen, Heikki Swan, Kirsi Piippo, et al.
World Journal of Gastroenterology|June 15, 2006
Family and twin studies in inflammatory bowel diseaseLeena Halme, Paulina Paavola-Sakki, Ulla Turunen, et al.
Journal of Molecular and Cellular Cardiology|July 28, 2004
Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndromeHeidi Fodstad, Heikki Swan, Muriel Auberson, et al.
Pharmacogenetics and Genomics|March 20, 2010
Common genetic variation of beta1- and beta2-adrenergic receptor and response to four classes of antihypertensive treatmentTimo Suonsyrjä, Kati Donner, Tuula Hannila-Handelberg, et al.
American Journal of Hypertension|December 6, 2008
Renin-angiotensin system and alpha-adducin gene polymorphisms and their relation to responses to antihypertensive drugs: results from the GENRES studyTimo Suonsyrjä, Tuula Hannila-Handelberg, Heidi Fodstad, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
International Journal of Cardiology|September 29, 2009
Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitroAnnukka Marjamaa, Päivi Laitinen-Forsblom, Anetta Wronska, et al.
Cardiovascular Research|May 26, 2005
Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insightsKimmo Kontula, Päivi J Laitinen, Annukka Lehtonen, et al.
European Journal of Endocrinology|October 19, 2012
Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1Kati M Donner, Timo P Hiltunen, Olli A Jänne, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|October 14, 2011
STK39 variation predicts the ambulatory blood pressure response to losartan in hypertensive menKati M Donner, Timo P Hiltunen, Tuula Hannila-Handelberg, et al.
International Journal of Legal Medicine|April 12, 2003
Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in waterPhilippe Lunetta, Antti Levo, Päivi J Laitinen, et al.
Annals of Medicine|June 5, 2004
Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardiaPäivi J Laitinen, Heikki Swan, Kirsi Piippo, et al.
World Journal of Gastroenterology|June 15, 2006
Family and twin studies in inflammatory bowel diseaseLeena Halme, Paulina Paavola-Sakki, Ulla Turunen, et al.
Journal of Molecular and Cellular Cardiology|July 28, 2004
Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndromeHeidi Fodstad, Heikki Swan, Muriel Auberson, et al.
Pharmacogenetics and Genomics|March 20, 2010
Common genetic variation of beta1- and beta2-adrenergic receptor and response to four classes of antihypertensive treatmentTimo Suonsyrjä, Kati Donner, Tuula Hannila-Handelberg, et al.
American Journal of Hypertension|December 6, 2008
Renin-angiotensin system and alpha-adducin gene polymorphisms and their relation to responses to antihypertensive drugs: results from the GENRES studyTimo Suonsyrjä, Tuula Hannila-Handelberg, Heidi Fodstad, et al.
Pageof 10