Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Elijah R. Behr"'
Autor:
Elijah R. Behr, Yanushi D. Wijeyeratne
Publikováno v:
Trends in Cardiovascular Medicine. 27:207-213
Approximately 4% of sudden cardiac deaths are unexplained [the sudden arrhythmic death syndrome (SADS)], and up to 6-10% of survivors of cardiac arrest do not have an identifiable cardiac abnormality after comprehensive clinical evaluation [idiopathi
Autor:
Elijah R. Behr, Kirsten Bartels, David J. Tester, Greg Mellor, Shubhayan Sanatani, Seshadri Balaji, Christopher S. Simpson, Pankaj Panwar, Christian Steinberg, Ngai Shing Mok, Richard Leather, Julie Hathaway, Andrew D. Krahn, Craig T. January, Christopher C. Erickson, Shelley Falik, Raul Weiss, Paul L. Eugenio, George McDaniel, Arthur A.M. Wilde, Nicole J. Boczek, Jason D. Roberts, Robert M. Hamilton, Elizabeth S. Kaufman, Zachary Laksman, Andrea K Y Lee, Susan Christian, Andrew E. Radbill, Michael J. Ackerman, Filip Van Petegem
Publikováno v:
EP Europace, 21(11), 1725-1732. Oxford University Press
Aims Pathogenic gain-of-function variants in CACAN1C cause type-8 long QT syndrome (LQT8). We sought to describe the electrocardiographic features in LQT8 and utilize molecular modelling to gain mechanistic insights into its genetic culprits. Methods
Autor:
Arthur A.M. Wilde, Elijah R. Behr
Publikováno v:
Nature reviews. Cardiology. 10(10):571-583
Over the past 2 decades, investigators in the field of cardiac genetics have evolved a complex understanding of the pathophysiological basis of inherited cardiac diseases, which predispose individuals to sudden cardiac death. In this Review, we descr
Autor:
Peter Weeke, Bram P. Prins, Yalda Jamshidi, Stefan Kääb, Margherita Torchio, Evmorfia Petropoulou, Dan M. Roden, Sanjay Sharma, Eline A. Nannenberg, Lia Crotti, Pascale Guicheney, Javad Jabbari, Julien Barc, Tao Yang, Peter J. Schwartz, Anders G. Holst, Eleonora Savio-Galimberti, Morten S. Olesen, Michael J. Ackerman, Connie R. Bezzina, Vincent Probst, Yuka Mizusawa, Dawood Darbar, Elijah R. Behr, Arthur A.M. Wilde, Myriam Berthet, Rachel Bastiaenan, Richard Redon, Antoine Leenhardt, Federica Dagradi, Stig Haunsø, Jacob Tfelt-Hansen
Publikováno v:
Cardiovascular Research
Cardiovascular Research, Oxford University Press (OUP), 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Cardiovascular Research, 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Cardiovascular research, 106(3), 520-529. Oxford University Press
Cardiovascular Research, Oxford University Press (OUP), 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Cardiovascular Research, 2015, Equipe 3 Equipe 4, 106 (3), pp.520--529. ⟨10.1093/cvr/cvv042⟩
Cardiovascular research, 106(3), 520-529. Oxford University Press
International audience; AIMS: Brugada syndrome (BrS) remains genetically heterogeneous and is associated with slowed cardiac conduction. We aimed to identify genetic variation in BrS cases at loci associated with QRS duration. METHODS AND RESULTS: A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1cdb672ac45c09cf337599dad400da7
http://hdl.handle.net/10281/182204
http://hdl.handle.net/10281/182204
Autor:
Dan M. Roden, Koji Miyamoto, Elijah R. Behr, Pascal P. McKeown, Shiro Kamakura, Minoru Horie, Peter J. Schwartz, Wataru Shimizu, Hideki Itoh, Michael Christiansen, Naomasa Makita, Shigetomo Fukuhara, Eric Schulze-Bahr, Alfred L. George, Takeru Makiyama, Naoki Mochizuki, Hiroyuki Tsutsui, Akihiko Sunami, Lia Crotti
Phenotypic overlap of type 3 long QT syndrome (LQT3) with Brugada syndrome (BrS) is observed in some carriers of mutations in the Na channel SCN5A. While this overlap is important for patient management, the clinical features, prevalence, and mechani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ed12e0ae2c340b0f219a52b9938202
http://hdl.handle.net/10281/189716
http://hdl.handle.net/10281/189716