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Kimmo Kontula

Showing results (21-30 of 97) with videos related to

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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 14, 2005
The relation of the XbaI and PvuII polymorphisms of the estrogen receptor gene and the CAG repeat polymorphism of the androgen receptor gene to peak bone mass and bone turnover rate among young healthy menVille-Valtteri Välimäki, Kirsi Piippo, Stiina Välimäki, et al.
Inflammatory Bowel Diseases|October 18, 2007
Novel CARD15/NOD2 mutations in Finnish patients with Crohn's disease and their relation to phenotypic variation in vitro and in vivoMaarit Lappalainen, Paulina Paavola-Sakki, Leena Halme, et al.
Annals of Medicine|June 25, 2009
Depressive symptoms in the congenital long QT syndromeTaina Hintsa, Liisa Keltikangas-Järvinen, Sampsa Puttonen, et al.
Hormone Research|March 30, 2005
Manifestation, management and molecular analysis of candidate genes in two rare cases of thyrotoxic hypokalemic periodic paralysisCamilla Schalin-Jantti, Tiina Laine, Kaisa Valli-Jaakola, et al.
Scandinavian Journal of Gastroenterology|April 26, 2006
Screening of tumor necrosis factor receptor-associated factor 6 as a candidate gene for inflammatory bowel diseaseMaarit Lappalainen, Paulina Paavola-Sakki, Leena Halme, et al.
Heart Rhythm|May 7, 2022
Effects of β-blockers on ventricular repolarization documented by 24-hour electrocardiography in long QT syndrome type 2Mikael Koponen, Annukka Marjamaa, Heikki Väänänen, et al.
BMC Medical Genetics|February 17, 2009
Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardiaAnnukka Marjamaa, Päivi Laitinen-Forsblom, Annukka M Lahtinen, et al.
Springerplus|March 31, 2016
Effects of cardioactive drugs on human induced pluripotent stem cell derived long QT syndrome cardiomyocytesJukka Kuusela, Ville J Kujala, Anna Kiviaho, et al.
Plos One|May 9, 2015
Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC ModelsKirsi Penttinen, Heikki Swan, Sari Vanninen, et al.
Annals of Medicine|June 5, 2004
Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in FinlandHeidi Fodstad, Heikki Swan, Päivi Laitinen, et al.
Pageof 10

Showing results (21-30 of 97) with videos related to

Sort By:
Pageof 10
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 14, 2005
The relation of the XbaI and PvuII polymorphisms of the estrogen receptor gene and the CAG repeat polymorphism of the androgen receptor gene to peak bone mass and bone turnover rate among young healthy menVille-Valtteri Välimäki, Kirsi Piippo, Stiina Välimäki, et al.
Inflammatory Bowel Diseases|October 18, 2007
Novel CARD15/NOD2 mutations in Finnish patients with Crohn's disease and their relation to phenotypic variation in vitro and in vivoMaarit Lappalainen, Paulina Paavola-Sakki, Leena Halme, et al.
Annals of Medicine|June 25, 2009
Depressive symptoms in the congenital long QT syndromeTaina Hintsa, Liisa Keltikangas-Järvinen, Sampsa Puttonen, et al.
Hormone Research|March 30, 2005
Manifestation, management and molecular analysis of candidate genes in two rare cases of thyrotoxic hypokalemic periodic paralysisCamilla Schalin-Jantti, Tiina Laine, Kaisa Valli-Jaakola, et al.
Scandinavian Journal of Gastroenterology|April 26, 2006
Screening of tumor necrosis factor receptor-associated factor 6 as a candidate gene for inflammatory bowel diseaseMaarit Lappalainen, Paulina Paavola-Sakki, Leena Halme, et al.
Heart Rhythm|May 7, 2022
Effects of β-blockers on ventricular repolarization documented by 24-hour electrocardiography in long QT syndrome type 2Mikael Koponen, Annukka Marjamaa, Heikki Väänänen, et al.
BMC Medical Genetics|February 17, 2009
Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardiaAnnukka Marjamaa, Päivi Laitinen-Forsblom, Annukka M Lahtinen, et al.
Springerplus|March 31, 2016
Effects of cardioactive drugs on human induced pluripotent stem cell derived long QT syndrome cardiomyocytesJukka Kuusela, Ville J Kujala, Anna Kiviaho, et al.
Plos One|May 9, 2015
Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC ModelsKirsi Penttinen, Heikki Swan, Sari Vanninen, et al.
Annals of Medicine|June 5, 2004
Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in FinlandHeidi Fodstad, Heikki Swan, Päivi Laitinen, et al.
Pageof 10