Lone atrial fibrillation in vigorously exercising middle aged men: case-control study

di Karjalainen, Jouko, Kujala, Urho M, Kaprio, Jaakko, Sarna, Seppo, Viitasalo, Matti
Pubblicazione 1998

Risk stratification in Brugada syndrome

di Glatter, Kathryn A, Chiamvimonvat, Nipavan, Viitasalo, Matti, Wang, Qing, Tuteja, Dipika
Pubblicazione 2005

Electrocardiographic Transmural Dispersion of Repolarization in Patients with Inherited Short QT Syndrome

di Anttonen, Olli, Väänänen, Heikki, Junttila, Juhani, Huikuri, Heikki V., Viitasalo, Matti
Pubblicato in Ann Noninvasive Electrocardiol (2008)

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

di Hekkala, Anna‐Mari, Swan, Heikki, Viitasalo, Matti, Väänänen, Heikki, Toivonen, Lauri
Pubblicato in Ann Noninvasive Electrocardiol (2011)

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

di Hekkala, Anna‐Mari, Väänänen, Heikki, Swan, Heikki, Oikarinen, Lasse, Viitasalo, Matti, Toivonen, Lauri
Pubblicato in Ann Noninvasive Electrocardiol (2006)

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

di Haapalahti, Petri, Viitasalo, Matti, Perhonen, Merja, Väänänen, Heikki, Mäkijärvi, Markku, Swan, Heikki, Toivonen, Lauri
Pubblicazione 2011

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

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

Sensitivity and Specificity of Automated Detection of Early Repolarization in Standard 12‐Lead Electrocardiography

di Kenttä, Tuomas, Porthan, Kimmo, Tikkanen, Jani T., Väänänen, Heikki, Oikarinen, Lasse, Viitasalo, Matti, Karanko, Hannu, Laaksonen, Maarit, Huikuri, Heikki V.
Pubblicato in Ann Noninvasive Electrocardiol (2014)

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

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

RELATIONSHIP OF COMMON CANDIDATE GENE VARIANTS TO ELECTROCARDIOGRAPHIC T-WAVE PEAK TO T-WAVE END INTERVAL AND T-WAVE MORPHOLOGY PARAMETERS

di Porthan, Kimmo, Marjamaa, Annukka, Viitasalo, Matti, Väänänen, Heikki, Jula, Antti, Toivonen, Lauri, Nieminen, Markku S, Newton-Cheh, Christopher, Salomaa, Veikko, Kontula, Kimmo, Oikarinen, Lasse
Pubblicazione 2010

Fibrosis and wall thickness affect ventricular repolarization dynamics in hypertrophic cardiomyopathy

di Jalanko, Mikko, Väänänen, Heikki, Tarkiainen, Mika, Sipola, Petri, Jääskeläinen, Pertti, Lauerma, Kirsi, Laitinen, Tiina, Laitinen, Tomi, Laine, Mika, Heliö, Tiina, Kuusisto, Johanna, Viitasalo, Matti
Pubblicato in Ann Noninvasive Electrocardiol (2018)

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

di 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
Pubblicato in BMC Med Genet (2018)

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

di 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
Pubblicazione 2012

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

di 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
Pubblicazione 2009

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

di 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
Pubblicazione 2009

A COMMON VARIANT NEAR KCNJ2 GENE IS ASSOCIATED WITH T-PEAK TO T-END INTERVAL

di Marjamaa, Annukka, Oikarinen, Lasse, Porthan, Kimmo, Ripatti, Samuli, Peloso, Gina, Noseworthy, Peter, Viitasalo, Matti, Nieminen, Markku S., Toivonen, Lauri, Kontula, Kimmo, Peltonen, Leena, Havulinna, Aki S., Jula, Antti, O’Donnell, Christopher J., Newton-Cheh, Christopher, Perola, Markus, Salomaa, Veikko
Pubblicazione 2012