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Journal of the American Heart Association|December 3, 2015
Blood Pressure Control and Risk of Stroke or Systemic Embolism in Patients With Atrial Fibrillation: Results From the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) TrialMeena P Rao, Sigrun Halvorsen, Daniel Wojdyla, et al.Journal of the American College of Cardiology|March 10, 2018
Digoxin and Mortality in Patients With Atrial FibrillationRenato D Lopes, Roberto Rordorf, Gaetano M De Ferrari, et al.Neuromuscular Disorders : NMD|January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) geneHaiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.Blood|October 17, 2014
Management and clinical outcomes in patients treated with apixaban vs warfarin undergoing proceduresDavid Garcia, John H Alexander, Lars Wallentin, et al.Blood|March 31, 2017
Intracranial hemorrhage in patients with atrial fibrillation receiving anticoagulation therapyRenato D Lopes, Patrícia O Guimarães, Bradley J Kolls, et al.Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathyCamila Armirola-Ricaurte, Laura Morant, Isabelle Adant, et al.Circulation. Heart Failure|April 12, 2013
Left ventricular systolic dysfunction, heart failure, and the risk of stroke and systemic embolism in patients with atrial fibrillation: insights from the ARISTOTLE trialJohn J V McMurray, Justin A Ezekowitz, Basil S Lewis, et al.European Heart Journal|October 23, 2013
Apixaban vs. warfarin with concomitant aspirin in patients with atrial fibrillation: insights from the ARISTOTLE trialJohn H Alexander, Renato D Lopes, Laine Thomas, et al.Brain : a Journal of Neurology|August 20, 2025
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathyCamila Armirola-Ricaurte, Laura Morant, Isabelle Adant, et al.Neuromuscular Disorders : NMD|November 16, 2019
MYO-MRI diagnostic protocols in genetic myopathiesJodi Warman Chardon, Jordi Díaz-Manera, Giorgio Tasca, et al.Pageof 13