Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Babar Parvez"'
Autor:
Jay A. Montgomery, MD, Wissam Abdallah, MD, Zachary T. Yoneda, MD, Evan Brittain, MD, MSCI, Sam G. Aznaurov, Babar Parvez, MD, Keith Adkins, RN, MSN, S. Patrick Whalen, MD, J.C. Estrada, MD, Sharon Shen, MD, George H. Crossley, MD, Arvindh Kanagasundram, MD, Pablo Saavedra, MD, Christopher R. Ellis, MD, Mark Lawson, MD, Dawood Darbar, MD, M. Benjamin Shoemaker, MD, MSCI
Publikováno v:
Journal of Arrhythmia, Vol 32, Iss 1, Pp 51-56 (2016)
Background: Atrial fibrillation (AF) is associated with cardiac fibrosis, which can now be measured noninvasively using T1-mapping with cardiac magnetic resonance imaging (CMRI). This study aimed to assess the impact of AF on ventricular T1 at the ti
Externí odkaz:
https://doaj.org/article/9263c183f76043f5888900491ce1f078
Publikováno v:
Case Reports in Medicine, Vol 2011 (2011)
Hypercalcemia is a relatively common clinical problem in both outpatient and inpatient settings. Primary pathophysiology is the entry of calcium that exceeds its excretion into urine or deposition in bone into circulation. Among a wide array of cause
Externí odkaz:
https://doaj.org/article/0a937edb912f4ea1b0a4b0cd5fe2d0bb
Publikováno v:
Journal of Innovations in Cardiac Rhythm Management. 7:2548-2552
Autor:
Dan M. Roden, Babar Parvez, Tanya Stubblefield, Gayle Kucera, Raafia Muhammad, Matthew J. Kolek, Joshua C. Denny, Marcia Blair, Dawood Darbar, M. Benjamin Shoemaker
Publikováno v:
The American Journal of Cardiology. 113:309-313
Single nucleotide polymorphisms (SNPs) at chromosome 4q25 (near PITX2) are strongly associated with atrial fibrillation (AF). We assessed whether a 4q25-tagging SNP (rs2200733) is associated with PR interval duration in patients with lone and typical
Autor:
Marcia Blair, Peter Weeke, Babar Parvez, Dan M. Roden, Christie Ingram, Dawood Darbar, Tanya Stubblefield, Laura Short, Gayle Kucera
Publikováno v:
Heart Rhythm. 11:46-52
Background Rare variants in candidate atrial fibrillation (AF) genes have been associated with AF in small kindreds. The extent to which such polymorphisms contribute to AF is unknown. Objective The purpose of this study was to determine the spectrum
Autor:
Babar Parvez, Shannon Carter, Dan M. Roden, Dawood Darbar, Shane Rowan, Tanya Stubblefield, Joseph Vaglio, Gayle Kucera, Raafia Muhammad
Publikováno v:
Journal of the American College of Cardiology. 60:539-545
ObjectivesThis study tested the hypothesis that response to antiarrhythmic drugs (AADs) is modulated by 3 common loci associated with atrial fibrillation (AF).BackgroundRecent genome-wide association studies have identified 3 loci, on chromosomes 4q2
Autor:
Ken Monahan, Babar Parvez, Sandeep Goyal, Dawood Darbar, Dan M. Roden, Li Wang, Jordan Brewster
Publikováno v:
The American Journal of Cardiology. 110:369-372
Atrial fibrillation (AF) is more common in those with obstructive sleep apnea (OSA) than in unaffected subjects and recurs more frequently in the presence of severe OSA after electrical cardioversion and AF ablation. However, it is unknown whether th
Autor:
David J. Milan, Lenore J. Launer, Bruno H. Stricker, Yongmei Liu, Arne Pfeufer, Jingzhong Ding, Jason D. Roberts, Vilmundur Gudnason, David Conen, Usha B. Tedrow, Eric Boerwinkle, Aravinda Chakravarti, Benjamin F. Voight, Michiel Rienstra, Emelia J. Benjamin, Guo Li, Dan E. Arking, Raafia Muhammad, Joshua C. Bis, Uwe Völker, Tatsuhiko Tsunoda, Mina K. Chung, Barbara McKnight, Lin Y. Chen, Sekar Kathiresan, Karen L. Furie, Kathryn L. Lunetta, Olle Melander, Kenneth Rice, Marylyn D. Ritchie, Honghuang Lin, Naoyuki Kamatani, Nicole L. Glazer, Kurt Lohman, W. H. Linda Kao, Jacqueline C.M. Witteman, Stefan Kääb, David R. Van Wagoner, Martina Müller-Nurasyid, Gerhard Steinbeck, Susan R. Heckbert, André G. Uitterlinden, Sebastian Clauss, Anne B. Newman, John Barnard, Nicholas L. Smith, Paul M. Ridker, Bruce M. Psaty, Dawood Darbar, Tamara B. Harris, Thomas Meitinger, Fernando Rivadeneira, Saagar Mahida, Marcus Dörr, Stephan B. Felix, J. Gustav Smith, Nona Sotoodehnia, Matthew Borkovich, Babar Parvez, Michiaki Kubo, Jonathan D. Smith, Albert Hofman, Tetsushi Furukawa, Kouichi Ozaki, Lynda M. Rose, Albert V. Smith, Jared W. Magnani, Toshihiro Tanaka, Steven A. Lubitz, Reza Wakili, Daniel Levy, Siyan Xu, Moritz F. Sinner, Robert W. Davies, H-Erich Wichmann, Elsayed Z. Soliman, Alvaro Alonso, Bouwe P. Krijthe, Dan M. Roden, Michael H. Gollob, Daniel I. Chasman, Marketa Sjögren, Siegfried Perz, Henry Völzke, Christine M. Albert, Yusuke Nakamura, Patrick T. Ellinor, Jerome I. Rotter, Jonathan Rosand
Publikováno v:
Nature Genetics, 44(6), 670-U88. Nature Publishing Group
Nature genetics
Nature Genetics, 44(6), 670-5. Nature Publishing Group
Nat. Genet. 44, 670-675 (2012)
Nature genetics
Nature Genetics, 44(6), 670-5. Nature Publishing Group
Nat. Genet. 44, 670-675 (2012)
Atrial fibrillation is a highly prevalent arrhythmia and a major risk factor for stroke, heart failure and death. We conducted a genome-wide association study (GWAS) in individuals of European ancestry, including 6,707 with and 52,426 without atrial
Autor:
Babar Parvez, Dan M. Roden, Joseph Vaglio, Shane Rowan, Raafia Muhammad, Dawood Darbar, Nagesh Chopra
Publikováno v:
Journal of the American College of Cardiology. 59:49-56
Objectives In this study, we evaluated the impact of 2 common β1-adrenergic receptor (β1-AR) polymorphisms ( G389R and S49G ) in response to ventricular rate control therapy in patients with atrial fibrillation (AF). Background Randomized studies h
Autor:
Gisli Masson, Daniel F. Gudbjartsson, Hilma Holm, Raafia Muhammad, Thomas Werge, Kari Stefansson, Gu∂mundur Thorgeirsson, Dawood Darbar, Carlo Zanon, Lambertus A. Kiemeney, Arnaldur Gylfason, Babar Parvez, Gudmar Thorleifsson, Hafdis T. Helgadottir, Dan M. Roden, Solveig Gretarsdottir, Hrafnhildur Stefansdottir, Jona Saemundsdottir, Thorunn Rafnar, Agnar Helgason, Aslaug Jonasdottir, Unnur Thorsteinsdottir, Augustine Kong, David O. Arnar, Stefan E Matthiasson, Asgeir Sigurdsson, G. Bragi Walters, Patrick Sulem, Hreinn Stefansson, Olafur T. Magnusson
Publikováno v:
Nature Genetics, 43, 4, pp. 316-20
Nature Genetics, 43, 316-20
Nature Genetics, 43, 316-20
Contains fulltext : 95597.pdf (Publisher’s version ) (Closed access) Through complementary application of SNP genotyping, whole-genome sequencing and imputation in 38,384 Icelanders, we have discovered a previously unidentified sick sinus syndrome