Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Kathleen R. Maginot"'
Autor:
Hanora A. Van Ert, BSN, Elise C. McCune, Kate M. Orland, MS, Kathleen R. Maginot, MD, Nicholas H. Von Bergen, MD, Craig T. January, MD, PhD, Lee L. Eckhardt, MD, FHRS
Publikováno v:
HeartRhythm Case Reports, Vol 3, Iss 2, Pp 151-154 (2017)
Externí odkaz:
https://doaj.org/article/b47d1738642b41beb28395a0234d54f1
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
An asymptomatic 5-year-old girl presented with bradycardia during a routine well-child visit. Further evaluation revealed profound sinus bradycardia, exercise-induced bidirectional ventricular tachycardia, and supraventricular tachycardia. An echocar
Externí odkaz:
https://doaj.org/article/cbd36ad39d374bb7abd035221453925a
Publikováno v:
Case Reports in Pediatrics, Vol 2012 (2012)
Atrial fibrillation (AF) is rare in the pediatric population; however, there is increasing recognition that AF can be inherited. Long QT syndrome (LQTS), likewise, can be both acquired and inherited with mutations leading to abnormalities in cardiac
Externí odkaz:
https://doaj.org/article/02c73256ab9a44c18a77d3949073db89
Autor:
Wei Zhou, Dan Ye, David J. Tester, Sahej Bains, John R. Giudicessi, Carla M. Haglund-Turnquist, Kate M. Orland, Craig T. January, Lee L. Eckhardt, Kathleen R. Maginot, Michael J. Ackerman
Publikováno v:
Circulation: Genomic and Precision Medicine. 16
Background: Long-QT syndrome (LQTS) is characterized by QT prolongation and increased risk for syncope, seizures, and sudden cardiac death. The majority of LQTS stems from pathogenic mutations in KCNQ1 , KCNH2 , or SCN5A . However, ≈10% of patients
Autor:
Wei Zhou, Dan Ye, David Tester, Sahej Bains, John R. Giudicessi, Carla Haglund-Turnquist, Kate Orland, Craig T. January, L. Lee Eckhardt, Kathleen R. Maginot, Michael John Ackerman
Publikováno v:
Heart Rhythm. 19:S165-S166
Autor:
Antoine Leenhardt, Shubhayan Sanatani, Susan P. Etheridge, Caitlin Brateng, Tomas Robyns, Isabelle Denjoy, Christopher Semsarian, Allan C. Skanes, Andrea Mazzanti, Jaimie Manlucu, Natalia Jura, Rahul C. Deo, Sean Connors, Andrew D. Krahn, Seshadri Balaji, Benjamin Pang, Michael J. Ackerman, Robert M. Hamilton, Julia Cadrin-Tourigny, Jason D. Roberts, Craig T. January, Arthur A.M. Wilde, Anthony Tang, Alice Maltret, Erron W. Titus, J. Martijn Bos, Silvia G. Priori, Dominic Abrams, Jeremy Wu, Martin S. Green, Frederick H. Deiter, Julie Rutberg, Jodie Ingles, Kevin Ng, Jeff S. Healey, Jan Till, Krystien V.V. Lieve, Lee L. Eckhardt, Christian van der Werf, Stephen A. Duffett, Peter S. Fischbach, Kathryn K. Collins, Kathleen R. Maginot, Kate M. Orland, Thomas M. Roston, Ferran Rosés I. Noguer, Linda M. Knight, Michael H. Gollob, Melvin M. Scheinman, Christian Steinberg
Publikováno v:
Circulation
Circulation, 142(10), 932-947. Lippincott Williams and Wilkins
Circulation, American Heart Association, 2020, 142 (10), pp.932-947. ⟨10.1161/CIRCULATIONAHA.120.045723⟩
Circulation, vol 142, iss 10
Circulation, 142(10), 932-947. Lippincott Williams and Wilkins
Circulation, American Heart Association, 2020, 142 (10), pp.932-947. ⟨10.1161/CIRCULATIONAHA.120.045723⟩
Circulation, vol 142, iss 10
Background:Genetic variants in calsequestrin-2 (CASQ2) cause an autosomal recessive form of catecholaminergic polymorphic ventricular tachycardia (CPVT), although isolated reports have identified arrhythmic phenotypes among heterozygotes. Improved in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f65dd090adfafecad5435b8af35536a
https://europepmc.org/articles/PMC7484339/
https://europepmc.org/articles/PMC7484339/
Autor:
Thomas M. Roston, Jeffrey M. Vinocur, Martin J. LaPage, Robert M. Hamilton, Kathleen R. Maginot, Shubhayan Sanatani, Wenting Guo, Ruiwu Wang, Arthur A.M. Wilde, Jan Till, Jinhong Wei, S.R. Wayne Chen, Lee L. Eckhardt, Andrew D. Krahn, Rafik Tadros, Puck Peltenburg, John Paul Estillore, Xiaowei Zhong, Kate M. Orland, Henrik Jensen, Jason D. Roberts, Yanhui Li
Publikováno v:
Heart Rhythm. 18:S288
Autor:
Lee L. Eckhardt, Nicholas H. Von Bergen, Kathleen R. Maginot, Craig T. January, Elise C. McCune, Kate M. Orland, Hanora Van Ert
Publikováno v:
HeartRhythm Case Reports
HeartRhythm Case Reports, Vol 3, Iss 2, Pp 151-154 (2017)
HeartRhythm Case Reports, Vol 3, Iss 2, Pp 151-154 (2017)
Autor:
Zhiguang Yuchi, Martin J. LaPage, Anjan S. Batra, Shubhayan Sanatani, Michal J. Kantoch, Sally H.J. Choi, Susan P. Etheridge, Chris Anderson, Thomas M. Roston, Yung R. Lau, Maria Miszczak-Knecht, Jeffrey M. Vinocur, Roman Gebauer, Christopher L. Johnsrude, Michel Cabrera Ortega, Ming-Lon Young, Saira Mohammed, Robert M. Hamilton, Jack C. Salerno, James E. Potts, Kathryn K. Collins, Ronald J. Kanter, Peter Kubuš, Julie Hathaway, Filip Van Petegem, Andreas Pflaumer, Lynn Kimlicka, Prince J. Kannankeril, Joel Temple, Vincent C. Thomas, Anne Fournier, Mitchell I. Cohen, Christopher C. Erickson, Yaniv Bar-Cohen, Kathleen R. Maginot, Gabriele Hessling
Publikováno v:
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, vol 20, iss 3
AIMS: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an ion channelopathy characterized by ventricular arrhythmia during exertion or stress. Mutations in RYR2-coded Ryanodine Receptor-2 (RyR2) and CASQ2-coded Calsequestrin-2 (CASQ2)
Publikováno v:
HeartRhythm Case Reports
Atrial arrhythmias, such as intraatrial reentrant tachycardia (IART) or atrial fibrillation, are commonly seen in older adults and in those with palliated congenital heart disease. With appropriate monitoring, especially at the time of initiation, so