Zobrazeno 1 - 10
of 182
pro vyhledávání: '"Michael H Gollob"'
Autor:
Lisa Albertini, Jordan Ezekian, Melanie Care, Candice Silversides, Mathew Sermer, Michael H. Gollob, Danna Spears
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 23 (2023)
Background It has been postulated that long QT syndrome (LQTS) can cause fetal loss through putative adverse effects of the channelopathy on placenta and myometrial function. The authors aimed to describe the fetal death rate in a population of pregn
Externí odkaz:
https://doaj.org/article/2265ccf302714d93af98bc62a6d52bf7
Autor:
Arthur A. M. Wilde, Christopher Semsarian, Manlio F. Márquez, Alireza Sepehri Shamloo, Michael J. Ackerman, Euan A. Ashley, Back Sternick Eduardo, Héctor Barajas‐Martinez, Elijah R. Behr, Connie R. Bezzina, Jeroen Breckpot, Philippe Charron, Priya Chockalingam, Lia Crotti, Michael H. Gollob, Steven Lubitz, Naomasa Makita, Seiko Ohno, Martín Ortiz‐Genga, Luciana Sacilotto, Eric Schulze‐Bahr, Wataru Shimizu, Nona Sotoodehnia, Rafik Tadros, James S. Ware, David S. Winlaw, Elizabeth S. Kaufman, Takeshi Aiba, Andreas Bollmann, Jong‐Il Choi, Aarti Dalal, Francisco Darrieux, John Giudicessi, Mariana Guerchicoff, Kui Hong, Andrew D. Krahn, Ciorsti Mac Intyre, Judith A. Mackall, Lluís Mont, Carlo Napolitano, Pablo Ochoa Juan, Petr Peichl, Alexandre C. Pereira, Peter J. Schwartz, Jon Skinner, Christoph Stellbrink, Jacob Tfelt‐Hansen, Thomas Deneke
Publikováno v:
Journal of Arrhythmia, Vol 38, Iss 4, Pp 491-553 (2022)
Externí odkaz:
https://doaj.org/article/065b869d10df4d35a27b0f57e20fcc2b
Autor:
Gan-Xiao Chen, Hector Barajas-Martínez, Giuseppe Ciconte, Cheng-I Wu, Michelle M. Monasky, Hao Xia, Bian Li, John A. Capra, Kai Guo, Zhong-He Zhang, Xiu Chen, Bo Yang, Hong Jiang, Gary Tse, Chloe Miu Mak, Yoshiyasu Aizawa, Michael H. Gollob, Charles Antzelevitch, Arthur A.M. Wilde, Carlo Pappone, Dan Hu
Publikováno v:
EBioMedicine, Vol 87, Iss , Pp 104388- (2023)
Summary: Background: Brugada syndrome (BrS) is a severe inherited arrhythmia syndrome that can be unmasked by fever. Methods: A multicentre clinical analysis was performed in 261 patients diagnosed with fever-induced BrS, including 198 (75.9%) and 27
Externí odkaz:
https://doaj.org/article/d15cdf54f8b04193a86c33c050c93e71
Autor:
Julie K. Wright, Darrell H. S. Tan, Sharon L. Walmsley, Jennifer Hulme, Erin O’Connor, Carolyn Snider, Ivy Cheng, Adrienne K. Chan, Bjug Borgundvaag, Shelley McLeod, Michael H. Gollob, Rosemarie J. Clarke, Linda Dresser, Fatima Haji, Tony Mazzulli, Samira Mubareka, Peter Jüni, Dominic Lee, George Tomlinson, Kevin C. Kain, Megan Landes
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-3 (2020)
Abstract Objectives Primary Objective: To determine if pre-exposure prophylaxis (PrEP) with 400mg hydroxychloroquine (HCQ), taken orally once daily reduces microbiologically confirmed COVID-19 among front line health care workers at high risk for SAR
Externí odkaz:
https://doaj.org/article/23c235c5f1014753bd2386bd25150636
Autor:
Dan Hu, Dong Hu, Liwen Liu, Daniel Barr, Yang Liu, Norma Balderrabano-Saucedo, Bo Wang, Feng Zhu, Yumei Xue, Shulin Wu, BaoLiang Song, Heather McManus, Katherine Murphy, Katherine Loes, Arnon Adler, Lorenzo Monserrat, Charles Antzelevitch, Michael H. Gollob, Perry M. Elliott, Hector Barajas-Martinez
Publikováno v:
EBioMedicine, Vol 54, Iss , Pp - (2020)
Background: Although 21 causative mutations have been associated with PRKAG2 syndrome, our understanding of the syndrome remains incomplete. The aim of this project is to further investigate its unique genetic background, clinical manifestations, and
Externí odkaz:
https://doaj.org/article/261fdad085bf4de79b25dd66139363da
Autor:
Michael H. Gollob
Publikováno v:
Heart Rhythm.
Autor:
Mey Boukenna, Prakash Arullampalam, Choshiman Taib, Sabrina Guichard, Jean-Sébastien Rougier, Michael H. Gollob, Hugues Abriel
BackgroundTRPM4 is a Ca2+-activated ion channel permeable to monovalent cations. Its expression in the heart has been confirmed, with most data supporting its presence in the conductive cardiac tissue. Numerous investigations have linkedTRPM4mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a76c6d80560a250e55adeb639106845
https://doi.org/10.1101/2023.03.29.534743
https://doi.org/10.1101/2023.03.29.534743
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
Autor:
Nathan Orr, Rima Arnaout, Lorne J. Gula, Danna A. Spears, Peter Leong-Sit, Qiuju Li, Wadea Tarhuni, Sven Reischauer, Vijay S. Chauhan, Matthew Borkovich, Shaheen Uppal, Arnon Adler, Shaun R. Coughlin, Didier Y. R. Stainier, Michael H. Gollob
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-8 (2016)
Here, Michael Gollob and colleagues perform a whole exome sequencing study to identify a mutation in the atrial-specific myosin light chain gene MYL4 in a small family with autosomal dominant familial atrial fibrillation. They also test the functiona
Externí odkaz:
https://doaj.org/article/3cbe2796738e4c49b3e6beec3f1f88fe
Autor:
Beatrice Bianchi, Lijo Cherian Ozhathil, Argelia Medeiros-Domingo, Michael H. Gollob, Hugues Abriel
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
Transient receptor potential melastatin member 4 (TRPM4), a non-selective cation channel, mediates cell membrane depolarization in immune response, insulin secretion, neurological disorders, and cancer. Pathological variants in TRPM4 gene have been l
Externí odkaz:
https://doaj.org/article/bd49b03986db476fbb85bc178ea5e278
Autor:
Emmi Helle, Lisa Albertini, Melanie Care, Ying Pei, Robert M. Hamilton, Vijay S. Chauhan, Michael H. Gollob, Danna A. Spears
Publikováno v:
Heart Rhythm. 20:S497-S498