Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients
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
Published in BMC medical genetics (05.04.2018)
Published in BMC medical genetics (05.04.2018)
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Not All hERG Pore Domain Mutations Have a Severe Phenotype: G584S Has an Inactivation Gating Defect with Mild Phenotype Compared to G572S, Which Has a Dominant Negative Trafficking Defect and a Severe Phenotype
ZHAO, JING TING, HILL, ADAM P., VARGHESE, ANTHONY, COOPER, ANTONY A., SWAN, HEIKKI, LAITINEN-FORSBLOM, PÄIVI J., REES, MARK I., SKINNER, JONATHAN R., CAMPBELL, TERENCE J., VANDENBERG, JAMIE I.
Published in Journal of cardiovascular electrophysiology (01.08.2009)
Published in Journal of cardiovascular electrophysiology (01.08.2009)
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Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients
Fodstad, Heidi, Bendahhou, Saïd, Rougier, Jean-Sébastien, Laitinen-Forsblom, Päivi J, Barhanin, Jacques, Abriel, Hugues, Schild, Laurent, Kontula, Kimmo, Swan, Heikki
Published in Annals of medicine (Helsinki) (01.01.2006)
Published in Annals of medicine (Helsinki) (01.01.2006)
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SCN5A Mutation Associated with Cardiac Conduction Defect and Atrial Arrhythmias
LAITINEN-FORSBLOM, PÄIVI J., MÄKYNEN, PEKKA, MÄKYNEN, HEIKKI, YLI-MÄYRY, SINIKKA, VIRTANEN, VESA, KONTULA, KIMMO, AALTO-SETÄLÄ, KATRIINA
Published in Journal of cardiovascular electrophysiology (01.05.2006)
Published in Journal of cardiovascular electrophysiology (01.05.2006)
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Gain-of-Function Mutation of the SCN5A Gene Causes Exercise-Induced Polymorphic Ventricular Arrhythmias
Swan, Heikki, Amarouch, Mohamed Yassine, Leinonen, Jaakko, Marjamaa, Annukka, Kucera, Jan P, Laitinen-Forsblom, Päivi J, Lahtinen, Annukka M, Palotie, Aarno, Kontula, Kimmo, Toivonen, Lauri, Abriel, Hugues, Widen, Elisabeth
Published in Circulation. Cardiovascular genetics (01.12.2014)
Published in Circulation. Cardiovascular genetics (01.12.2014)
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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
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
Published in BMC medical genetics (05.04.2018)
Published in BMC medical genetics (05.04.2018)
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Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves
Paavola, Jere, Viitasalo, Matti, Laitinen-Forsblom, Päivi J., Pasternack, Michael, Swan, Heikki, Tikkanen, Ilkka, Toivonen, Lauri, Kontula, Kimmo, Laine, Mika
Published in European heart journal (01.05.2007)
Published in European heart journal (01.05.2007)
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Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca[sup]2+ waves
Paavola, Jere, Viitasalo, Matti, Laitinen-Forsblom, Päivi J, Pasternack, Michael, Swan, Heikki, Tikkanen, Ilkka, Toivonen, Lauri, Kontula, Kimmo, Laine, Mika
Published in European heart journal (01.05.2007)
Published in European heart journal (01.05.2007)
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0265: A novel SCN5A mutation associated with exercise-induced polymorphic ventricular arrhythmias resembling CPVT
Amarouch, Mohamed Yassine, Leinonen, Jaakko, Marjamaa, Annukka, Kucera, Jan P., Laitinen-Forsblom, Päivi J., Lahtinen, Annukka M., Palotie, Aarno, Kontula, Kimmo, Toivonen, Lauri, Abriel, Hugues, Widen, Elisabeth, Swan, Heikki
Published in Archives of Cardiovascular Diseases Supplements (01.04.2014)
Published in Archives of Cardiovascular Diseases Supplements (01.04.2014)
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Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves. Commentary
WEHRENS, Xander H. T, PAAVOLA, Jere, VIITASALO, Matti, LAITINEN-FORSBLOM, Päivi J, PASTERNACK, Michael, SWAN, Heikki, TIKKANEN, Ilkka, TOIVONEN, Lauri, KONTULA, Kimmo, LAINE, Mika
Published in European heart journal (2007)
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Published in European heart journal (2007)
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