Myriam Berthet and Véronique Fressart - Free people check

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290 The KCNQ1 rs polymorphism is a genetic ...

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Sabine Duchatelet : Orateur, Rachel Peat, Isabelle Denjoy, Hideki Itoh, Myriam Berthet, Lia Crotti, Seiko Ohno, Véronique Fressart, Matteo Pedrazzini, ... › article

290 The KCNQ1 rs polymorphism is a genetic ...www.em-consulte.com › article

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Sabine Duchatelet : Orateur, Rachel Peat, Isabelle Denjoy, Hideki Itoh, Myriam Berthet, Lia Crotti, Seiko Ohno, Véronique Fressart, Matteo Pedrazzini, Didier ...

Archives of Cardiovascular Diseases Supplements - Présentation - EM...

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290 The KCNQ1 rs polymorphism is a genetic modifier of cardiac risk in long QT syndrome; Sabine Duchatelet, Rachel Peat, Isabelle Denjoy, Hideki Itoh, Myriam Berthet, Lia Crotti, Seiko Ohno, Véronique Fressart, Matteo Pedrazzini, Didier Klug, David-Alexandre Trégouët, Peter J. Schwartz, Wataru Shimizu, ...

EBSCOhost | | Novel SCN5A mutations in two families with...

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Veronique Fressart & Myriam Berthet & Isabelle Denjoy &. Nawal Bennamar & Anne Rollin & Christelle Cardin &. Pascale Guicheney & Mohamed Chahine. Received: 15 December Accepted: 20 March Published online: 24 April © Springer Science+Business Media New York Abstract.

preferential maternal transmission of KCNQ1 variants linked to ...

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by H Itoh · · Cited by 19 — Hideki Itoh , Myriam Berthet , Véronique Fressart , Isabelle Denjoy , Svetlana Maugenre , Didier Klug , Yuka Mizusawa , Takeru Makiyama , Nynke ... › ...

Long QT syndrome in neonates - CORE

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by JM Lupoglazoff · · Cited by 153 — Véronique Fressart, MD, Françoise Simon, André Bozio, MD,¶ Myriam Berthet,† Nawal Benammar,†. Bernard Hainque, PHD,† Pascale Guicheney, PHD†. › download › pdf

All web results to the name "Myriam Berthet"

Kuhn André, Viviane, Simon et Myriam - data-history.com

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2005: Laetitia Gouas; Viviane Nicaud; Myriam Berthet ... Elisabeth Villain; Véronique Fressart; Françoise Simon; André Bozio; Myriam Berthet ... du coeur et ... › company_...

PubMed Channelpedia - EPFL

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... Rachel Peat, Jean-Marc Lupoglazoff, Véronique Fressart, Myriam Berthet, Michael J Ackerman, Craig T January, Pascale Guicheney, Brian P Delisle. › pubmeds

Useful Resources | Long QT Syndrome Type 1

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Burgess, Didier Klug, Isabelle Denjoy, Rachel Peat, Jean-Marc Lupoglazoff, Véronique Fressart, Myriam Berthet, Michael J. Ackerman, Craig T. January, Pascale ... › useful-resources

Volume 20, numéro 2, février John Libbey Eurotext

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Véronique Fressart, Isabelle Denjoy, Jean-Marc Lupoglazoff, Antoine Leenhardt, Myriam Berthet, Pascale Guicheney, Bernard Hainque Article offert. › revues › stv › sommaire

289 Role of Krox20 during cardiac valve development, remodeling ...

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Article suivant 290 The KCNQ1 rs polymorphism is a genetic modifier of cardiac risk in long QT syndrome. Sabine Duchatelet, Rachel Peat, Isabelle Denjoy, Hideki Itoh, Myriam Berthet, Lia Crotti, Seiko Ohno, Véronique Fressart, Matteo Pedrazzini, Didier Klug, David-Alexandre Trégouët, Peter J. Schwartz, Wataru ...

An international compendium of mutations in the SCN5A-encoded cardiac...

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Jamie D. Kapplinger, David J. Tester, Marielle Alders, Begoña Benito, Myriam Berthet, Josep Brugada, Pedro Brugada, Véronique Fressart, Alejandra ...

Identification of a KCNQ1 Polymorphism Acting as Altmetricahajournals.altmetric.com › details

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Sabine Duchatelet, Lia Crotti, Rachel A. Peat, Isabelle Denjoy, Hideki Itoh, Myriam Berthet, Seiko Ohno, Véronique Fressart, Maria Cristina Monti, Cristina ...