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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, ...

All web results to the name "Myriam Berthet"

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

R231C mutation in KCNQ1 causes long QT syndrome type

mayoclinic.pure.elsevier.com

by DC Bartos · · Cited by 80 — Daniel C. Bartos, Sabine Duchatelet, Don E. Burgess, Didier Klug, Isabelle Denjoy, Rachel Peat, Jean Marc Lupoglazoff, Vronique Fressart, Myriam Berthet, ... › publications

Useful Resources | Long QT Syndrome Type 1

you.stonybrook.edu

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

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

emvmsa1a.jouve-hdi.com

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 ...