Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Guido D, Pollevick"'
Autor:
Rachel T. Klein, Xinxin (Shirley) Yao, Catherine Griswold, Adebanke F. Fagbemi, Lisa R. Susswein, Guido D. Pollevick
Publikováno v:
Obstetrics & Gynecology. 133:163-164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d91d9b81b4ade79072e99f7b88aadd6
https://doi.org/10.1097/01.aog.0000558868.23977.62
https://doi.org/10.1097/01.aog.0000558868.23977.62
Autor:
Rachel Nusbaum, Megan L. Marshall, Lauren Yackowski, Lisa R. Susswein, Scott M. Weissman, Kristen J. Vogel Postula, Patricia D. Murphy, Gabi Richard, Jeffrey Bissonnette, Erica M. Vaccari, Wendy K. Chung, Daniel E. Pineda-Alvarez, Jessica K. Booker, Sherri J. Bale, M. Laura Cremona, Rachel T. Klein, Guido D. Pollevick, Zhixiong Xu, Kathleen S. Hruska, Federica Gibellini
Publikováno v:
Genetics in Medicine
Purpose: Germ-line testing for panels of cancer genes using next-generation sequencing is becoming more common in clinical care. We report our experience as a clinical laboratory testing both well-established, high-risk cancer genes (e.g., BRCA1/2, M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54513942055a87a6c0069e6fe9baf282
http://europepmc.org/articles/PMC4985612
http://europepmc.org/articles/PMC4985612
Autor:
Rainer Schimpf, Michel Haïssaguerre, Samuel Zimmern, Mark Marieb, Guido D. Pollevick, Elena Burashnikov, Roberto Robles, Sami Viskin, Dan Hu, Ryan Pfeiffer, Charles Antzelevitch, Mayurika Desai, Ronald J. Kanter, Stephen L. Winters, Christian Wolpert, Dwight D. Stapleton, Gi-Byoung Nam, Christian Veltmann, Alejandra Guerchicoff, Ruben Laiño, Hector Barajas-Martinez, Eva Delpón, Martin Borggrefe, Koonlawee Nademanee
Publikováno v:
Heart Rhythm. 7:1872-1882
Background L-type calcium channel (LTCC) mutations have been associated with Brugada syndrome (BrS), short QT (SQT) syndrome, and Timothy syndrome (LQT8). Little is known about the extent to which LTCC mutations contribute to the J-wave syndromes ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b160c86cb47a6bc60dd640f0f3c94f05
https://doi.org/10.1016/j.hrthm.2010.08.026
https://doi.org/10.1016/j.hrthm.2010.08.026
Autor:
Yuesheng Wu, Elena Burashnikov, Tamara T. Koopmann, Jonathan M. Cordeiro, Charles Antzelevitch, Ryan Pfeiffer, Guido D. Pollevick, Alejandra Guerchicoff, András Varró, Michael Springer, Hector Barajas-Martinez, Dan Hu
Publikováno v:
Circulation. Cardiovascular genetics, 2(3), 270-278. Lippincott Williams and Wilkins
Background— Brugada syndrome, characterized by ST-segment elevation in the right precordial ECG leads and the development of life-threatening ventricular arrhythmias, has been associated with mutations in 6 different genes. We identify and characte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91069b772820838d95b635d20e348921
https://doi.org/10.1161/circgenetics.108.829192
https://doi.org/10.1161/circgenetics.108.829192
Autor:
Tabitha Carrier, Alexandra Guerchicoff, Dan Hu, Elena Burashnikov, Hector Barajas-Martinez, Jonathan M. Cordeiro, Vincenzo Lorenzo Pascali, Ramon Brugada, Yusheng Wu, Sami Viskin, Rafael Rosso, Guido D. Pollevick, Antonio Oliva, Charles Antzelevitch
Publikováno v:
Legal Medicine. 11:S206-S209
Ventricular tachycardia and fibrillation (VT/VF) complicating Brugada syndrome, a genetic disorder linked to SCN5A mutations, and VF complicating acute myocardial infarction (AMI) have both been linked to phase 2 reentry. Because of these mechanistic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8114be24b0dc79991cf6d0e6f1f4085d
https://doi.org/10.1016/j.legalmed.2009.02.044
https://doi.org/10.1016/j.legalmed.2009.02.044
Autor:
Yuesheng Wu, Jonathan M. Cordeiro, Charles Antzelevitch, Michael Christiansen, Carsten Toftager Larsen, Lucía Núñez, Alejandra Guerchicoff, Jacob Hofman-Bang, Eva Delpón, Poul Erik Bloch Thomsen, Elena Burashnikov, Jørgen K. Kanters, Guido D. Pollevick
Publikováno v:
Circulation: Arrhythmia and Electrophysiology. 1:209-218
Background— The Brugada syndrome, an inherited syndrome associated with a high incidence of sudden cardiac arrest, has been linked to mutations in 4 different genes, leading to a loss of function in sodium and calcium channel activity. Although the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26abc2b15c7565b629b78cf6c4f13e94
https://doi.org/10.1161/circep.107.748103
https://doi.org/10.1161/circep.107.748103
Autor:
Jonathan M. Cordeiro, Guido D. Pollevick, Charles Antzelevitch, Yoshiyasu Aizawa, Dan Hu, Alejandra Guerchicoff, Jacob Hofman-Bang, Stig Haunsø, Gorm B. Jensen, Lasse Steen Ravn, Jesper Hastrup Svendsen, Michael Christiansen, Yuesheng Wu, Elena Burashnikov, Ulrik Dixen
Publikováno v:
Heart Rhythm. 5:427-435
Background Atrial fibrillation (AF) is the most common clinical arrhythmia and a major cause of cardiovascular morbidity and mortality. Among the gene defects previously associated with AF is a gain of function of the slowly activating delayed rectif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f32b418214b8872a0bdd9cdfa4f244f
https://doi.org/10.1016/j.hrthm.2007.12.019
https://doi.org/10.1016/j.hrthm.2007.12.019
Autor:
Tabitha Carrier, Elena Burashnikov, Dan Hu, Jonathan M. Cordeiro, Rafael Rosso, Charles Antzelevitch, Guido D. Pollevick, Serge Sicouri, Ramon Brugada, Antonio Oliva, Yuesheng Wu, Sami Viskin, Alejandra Guerchicoff, Hector Barajas-Martinez
Publikováno v:
Heart Rhythm. 4:1072-1080
Background Ventricular tachycardia (VT) and ventricular fibrillation (VF) complicating Brugada syndrome, a genetic disorder linked to SCN5A mutations, and VF complicating acute myocardial infarction (AMI) both have been linked to phase 2 reentry. Obj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::976628e50214d13c69f2d1f8ddddccf8
https://doi.org/10.1016/j.hrthm.2007.03.040
https://doi.org/10.1016/j.hrthm.2007.03.040
Autor:
Charles Antzelevitch, Ramon Brugada, Guido D. Pollevick, Guillermo J. Pérez, Alejandra Guerchicoff, Fabiana S. Scornik, Mayurika Desai
Publikováno v:
Heart Rhythm. 3:842-850
Background The autonomic nervous system has been implicated in several arrhythmogenic diseases, including long QT syndrome type 3 (LQT3) and Brugada syndrome. Scarce information on the cellular components of the intrinsic cardiac ganglia from higher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca08ee2203c5564405b907922fd9227a
https://doi.org/10.1016/j.hrthm.2006.03.021
https://doi.org/10.1016/j.hrthm.2006.03.021
Autor:
Eberhard Fuchs, Guido D. Pollevick, Fernán Agüero, Julieta Alfonso, Gabriele Flügge, Alberto C.C. Frasch, Daniel O. Sánchez
Publikováno v:
Journal of Neuroscience Research. 78:702-710
Adrenal corticosteroids influence the function of the hippocampus, the brain structure in which the highest expression of glucocorticoid receptors is found. Chronic high levels of cortisol elicited by stress or through exogenous administration can ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::339467a2d2e1466f5a0174ceefdf139b
https://doi.org/10.1002/jnr.20328
https://doi.org/10.1002/jnr.20328