Hasil Pencarian - Lauri Toivonen

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  1. 1
    Flexibilidade da Programaçao Evita Intervençao Desnecessária em Pacientes com CDI

    Flexibilidade da Programaçao Evita Intervençao Desnecessária em Pacientes com CDI oleh St. Jude Medical, Dr. Lauri Toivonen*

    Diterbitkan 2009-10-01
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  2. 2
    Flexibilidade da Programaçao Evita Intervençao Desnecessária em Pacientes com CDI

    Flexibilidade da Programaçao Evita Intervençao Desnecessária em Pacientes com CDI oleh St. Jude Medical, Dr. Lauri Toivonen*

    Diterbitkan 2009-10-01
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  3. 3
    Flexibilidade da Programaçao Evita Intervençao Desnecessária em Pacientes com CDI

    Flexibilidade da Programaçao Evita Intervençao Desnecessária em Pacientes com CDI oleh St. Jude Medical, Dr. Lauri Toivonen*

    Diterbitkan 2009-10-01
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  4. 4
    Peak CK-MB has a strong association with chronic scar size and wall motion abnormalities after revascularized non-transmural myocardial infarction – a prospective CMR study

    Peak CK-MB has a strong association with chronic scar size and wall motion abnormalities after revascularized non-transmural myocardial infarction – a prospective CMR study oleh Pauli Pöyhönen, Minna Kylmälä, Paula Vesterinen, Sari Kivistö, Miia Holmström, Kirsi Lauerma, Heikki Väänänen, Lauri Toivonen, Helena Hänninen

    Diterbitkan 2018-02-01
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  5. 5
    Testing of Common Electromagnetic Environments for Risk of Interference with Cardiac Pacemaker Function

    Testing of Common Electromagnetic Environments for Risk of Interference with Cardiac Pacemaker Function oleh Maria Tiikkaja, Aapo L. Aro, Tommi Alanko, Harri Lindholm, Heli Sistonen, Juha E.K. Hartikainen, Lauri Toivonen, Jukka Juutilainen, Maila Hietanen

    Diterbitkan 2013-09-01
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  6. 6
    Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.

    Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. oleh Mikael Koponen, Annukka Marjamaa, Annukka M Tuiskula, Matti Viitasalo, Terhi Nallinmaa-Luoto, Jaakko T Leinonen, Elisabeth Widen, Lauri Toivonen, Kimmo Kontula, Heikki Swan

    Diterbitkan 2020-01-01
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  7. 7
    Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients

    Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients oleh Mikael Koponen, Aki S. Havulinna, Annukka Marjamaa, Annukka M. Tuiskula, Veikko Salomaa, Päivi J. Laitinen-Forsblom, Kirsi Piippo, Lauri Toivonen, Kimmo Kontula, Matti Viitasalo, Heikki Swan

    Diterbitkan 2018-04-01
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  8. 8
    Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations.

    Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations. oleh Kirsi Kujala, Jere Paavola, Anna Lahti, Kim Larsson, Mari Pekkanen-Mattila, Matti Viitasalo, Annukka M Lahtinen, Lauri Toivonen, Kimmo Kontula, Heikki Swan, Mika Laine, Olli Silvennoinen, Katriina Aalto-Setälä

    Diterbitkan 2012-01-01
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  9. 9
    Polymorphisms in the GNAS Gene as Predictors of Ventricular Tachyarrhythmias and Sudden Cardiac Death: Results From the DISCOVERY Trial and Oregon Sudden Unexpected Death Study

    Polymorphisms in the GNAS Gene as Predictors of Ventricular Tachyarrhythmias and Sudden Cardiac Death: Results From the DISCOVERY Trial and Oregon Sudden Unexpected Death Study oleh Heinrich Wieneke, Jesper Hastrup Svendsen, Jeffrey Lande, Sebastian Spencker, Juan Gabriel Martinez, Bernhard Strohmer, Lauri Toivonen, Hervé Le Marec, F. Javier Garcia‐Fernandez, Domenico Corrado, Adriana Huertas‐Vazquez, Audrey Uy‐Evanado, Carmen Rusinaru, Kyndaron Reinier, Csaba Foldesi, Wieslaw Hulak, Sumeet S. Chugh, Winfried Siffert

    Diterbitkan 2016-12-01
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