KCNE1 D85N polymorphism — a sex-specific modifier in type 1 long QT syndrome?

ανά Lahtinen, Annukka M, Marjamaa, Annukka, Swan, Heikki, Kontula, Kimmo
Έκδοση 2011

Epinephrine Bolus Test in Detecting Long QT Syndrome Mutation Carriers with Indeterminable Electrocardiographic Phenotype

ανά Hekkala, Anna‐Mari, Swan, Heikki, Viitasalo, Matti, Väänänen, Heikki, Toivonen, Lauri
Τόπος έκδοσης Ann Noninvasive Electrocardiol (2011)

Reproducibility of Computerized Measurements of QT Interval from Multiple Leads at Rest and During Exercise

ανά Hekkala, Anna‐Mari, Väänänen, Heikki, Swan, Heikki, Oikarinen, Lasse, Viitasalo, Matti, Toivonen, Lauri
Τόπος έκδοσης Ann Noninvasive Electrocardiol (2006)

Comparison of QT peak and QT end interval responses to autonomic adaptation in asymptomatic LQT1 mutation carriers

ανά Haapalahti, Petri, Viitasalo, Matti, Perhonen, Merja, Väänänen, Heikki, Mäkijärvi, Markku, Swan, Heikki, Toivonen, Lauri
Έκδοση 2011

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

ανά Marjamaa, Annukka, Laitinen-Forsblom, Päivi, Lahtinen, Annukka M, Viitasalo, Matti, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Έκδοση 2009

Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models

ανά Penttinen, Kirsi, Swan, Heikki, Vanninen, Sari, Paavola, Jere, Lahtinen, Annukka M., Kontula, Kimmo, Aalto-Setälä, Katriina
Τόπος έκδοσης PLoS One (2015)

Correction: Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models

ανά Penttinen, Kirsi, Swan, Heikki, Vanninen, Sari, Paavola, Jere, Lahtinen, Annukka M., Kontula, Kimmo, Aalto-Setälä, Katriina
Τόπος έκδοσης PLoS One (2015)

Effects of cardioactive drugs on human induced pluripotent stem cell derived long QT syndrome cardiomyocytes

ανά Kuusela, Jukka, Kujala, Ville J., Kiviaho, Anna, Ojala, Marisa, Swan, Heikki, Kontula, Kimmo, Aalto-Setälä, Katriina
Τόπος έκδοσης Springerplus (2016)

The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome

ανά Huttunen, Heta, Hero, Matti, Lääperi, Mitja, Känsäkoski, Johanna, Swan, Heikki, Hirsch, Joel A., Miettinen, Päivi J., Raivio, Taneli
Τόπος έκδοσης Front Endocrinol (Lausanne) (2018)

Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain‐of‐Function Mutation in the Na(v)1.5 Sodium Channel

ανά Amarouch, Mohamed Y., Swan, Heikki, Leinonen, Jaakko, Marjamaa, Annukka, Lahtinen, Annukka M., Kontula, Kimmo, Toivonen, Lauri, Widen, Elisabeth, Abriel, Hugues
Τόπος έκδοσης Ann Noninvasive Electrocardiol (2015)

Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation

ανά Koponen, Mikael, Marjamaa, Annukka, Tuiskula, Annukka M., Viitasalo, Matti, Nallinmaa-Luoto, Terhi, Leinonen, Jaakko T., Widen, Elisabeth, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Τόπος έκδοσης PLoS One (2020)

Distinct electrophysiological and mechanical beating phenotypes of long QT syndrome type 1-specific cardiomyocytes carrying different mutations

ανά Kiviaho, Anna L., Ahola, Antti, Larsson, Kim, Penttinen, Kirsi, Swan, Heikki, Pekkanen-Mattila, Mari, Venäläinen, Henna, Paavola, Kiti, Hyttinen, Jari, Aalto-Setälä, Katriina
Τόπος έκδοσης Int J Cardiol Heart Vasc (2015)

Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients: Koponen et al. Follow-up of adult LQTS patients

ανά Koponen, Mikael, Havulinna, Aki S., Marjamaa, Annukka, Tuiskula, Annukka M., Salomaa, Veikko, Laitinen-Forsblom, Päivi J., Piippo, Kirsi, Toivonen, Lauri, Kontula, Kimmo, Viitasalo, Matti, Swan, Heikki
Τόπος έκδοσης BMC Med Genet (2018)

Cell Model of Catecholaminergic Polymorphic Ventricular Tachycardia Reveals Early and Delayed Afterdepolarizations

ανά Kujala, Kirsi, Paavola, Jere, Lahti, Anna, Larsson, Kim, Pekkanen-Mattila, Mari, Viitasalo, Matti, Lahtinen, Annukka M., Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki, Laine, Mika, Silvennoinen, Olli, Aalto-Setälä, Katriina
Έκδοση 2012

Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture

ανά Lahti, Anna L., Kujala, Ville J., Chapman, Hugh, Koivisto, Ari-Pekka, Pekkanen-Mattila, Mari, Kerkelä, Erja, Hyttinen, Jari, Kontula, Kimmo, Swan, Heikki, Conklin, Bruce R., Yamanaka, Shinya, Silvennoinen, Olli, Aalto-Setälä, Katriina
Έκδοση 2012

COMMON CANDIDATE GENE VARIANTS ARE ASSOCIATED WITH QT INTERVAL DURATION IN THE GENERAL POPULATION

ανά Marjamaa, Annukka, Newton-Cheh, Christopher, Porthan, Kimmo, Reunanen, Antti, Lahermo, Päivi, Väänänen, Heikki, Jula, Antti, Karanko, Hannu, Swan, Heikki, Toivonen, Lauri, Nieminen, Markku S., Viitasalo, Matti, Peltonen, Leena, Oikarinen, Lasse, Palotie, Aarno, Kontula, Kimmo, Salomaa, Veikko
Έκδοση 2009

High prevalence of four long QT syndrome founder mutations in the Finnish population

ανά MARJAMAA, ANNUKKA, SALOMAA, VEIKKO, NEWTON-CHEH, CHRISTOPHER, PORTHAN, KIMMO, REUNANEN, ANTTI, KARANKO, HANNU, JULA, ANTTI, LAHERMO, PÄIVI, VÄÄNÄNEN, HEIKKI, TOIVONEN, LAURI, SWAN, HEIKKI, VIITASALO, MATTI, NIEMINEN, MARKKU S., PELTONEN, LEENA, OIKARINEN, LASSE, PALOTIE, AARNO, KONTULA, KIMMO
Έκδοση 2009

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

ανά Kerr, Shona M., Klaric, Lucija, Halachev, Mihail, Hayward, Caroline, Boutin, Thibaud S., Meynert, Alison M., Semple, Colin A., Tuiskula, Annukka M., Swan, Heikki, Santoyo-Lopez, Javier, Vitart, Veronique, Haley, Chris, Dean, John, Miedzybrodzka, Zosia, Aitman, Timothy J., Wilson, James F.
Τόπος έκδοσης Sci Rep (2019)

Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier against Arrhythmic Risk in Long QT Syndrome

ανά Duchatelet, Sabine, Crotti, Lia, Peat, Rachel A., Denjoy, Isabelle, Itoh, Hideki, Berthet, Myriam, Ohno, Seiko, Fressart, Véronique, Monti, Maria Cristina, Crocamo, Cristina, Pedrazzini, Matteo, Dagradi, Federica, Vicentini, Alessandro, Klug, Didier, Brink, Paul A., Goosen, Althea, Swan, Heikki, Toivonen, Lauri, Lahtinen, Annukka M., Kontula, Kimmo, Shimizu, Wataru, Horie, Minoru, George, Alfred L., Trégouët, David-Alexandre, Guicheney, Pascale, Schwartz, Peter J.
Έκδοση 2013

Heritability in genetic heart disease: the role of genetic background

ανά Jansweijer, Joeri A, van Spaendonck-Zwarts, Karin Y, Tanck, Michael W T, van Tintelen, J Peter, Christiaans, Imke, van der Smagt, Jasper J, Vermeer, Alexa M C, Bos, J Martijn, Moss, Arthur J, Swan, Heikki, Priori, Sylvia G, Rydberg, Annika, Tfelt-Hansen, Jacob, Ackerman, Michael J, Olivotto, Iacopo, Charron, Philippe, Gimeno, Juan R, van den Berg, Maarten P, Wilde, Arthur AM, Pinto, Yigal M
Τόπος έκδοσης Open Heart (2019)