Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Robyn J. Hylind"'
Autor:
Robyn J. Hylind, Stephanie F. Chandler, Virginie Beausejour Ladouceur, Shelina M. Jamal, Mark E. Alexander, Douglas Y. Mah, Emily A. Phaneuf, Elizabeth S. DeWitt, Vassilios J. Bezzerides, Dominic J. Abrams
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 10 (2020)
Externí odkaz:
https://doaj.org/article/e728e900105a4691b7096c5ba9b2d61d
Autor:
Robyn J. Hylind, Dominic J. Abrams
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 3 (2020)
Externí odkaz:
https://doaj.org/article/b5d3a2df889248ffa9b0f2414e2093fa
Autor:
Robyn J. Hylind, MS, CGC, Virginie Beausejour Ladouceur, MD, Francis Fynn-Thompson, MD, Shannon E. Hourigan, PhD, Vassilios J. Bezzerides, PhD, MD, Dominic J. Abrams, MD, MRCP
Publikováno v:
HeartRhythm Case Reports, Vol 4, Iss 1, Pp 14-17 (2018)
Externí odkaz:
https://doaj.org/article/92fc3a99c0f148a7b838f90d6a6d124f
Autor:
Kristina D. Chambers, Virginie Beausejour Ladouceur, Mark E. Alexander, Robyn J. Hylind, Laura Bevilacqua, Douglas Y. Mah, Vassilios Bezzerides, John K. Triedman, Edward P. Walsh, Dominic J. Abrams
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 6, Iss 9 (2017)
BackgroundThe 2005 Bethesda Conference Guidelines advise patients with long QT syndrome against competitive sports. We assessed cardiac event rates during competitive and recreational sports, and daily activities among treated long QT syndrome patien
Externí odkaz:
https://doaj.org/article/ec82f0c8d690433e8c895e0bcc697611
Autor:
Kelsey M. Fusco, Robyn J. Hylind, Allison L. Cirino, Stephanie L. Harris, Steven A. Lubitz, Dominic J.R. Abrams, Neal K. Lakdawala
Publikováno v:
Journal of Genetic Counseling. 31:1273-1281
First-degree relatives of a proband with an inherited cardiac condition (ICC) are offered predictive genetic testing for the pathogenic or likely pathogenic (P/LP) cardiac gene variant (CGV) to clarify their risk for the familial condition. Relatives
Autor:
Paloma Remior Pérez, Robyn J. Hylind, Thomas M. Roston, Vassilios J. Bezzerides, Dominic J. Abrams
Publikováno v:
Heart, Lung and Circulation.
Autor:
Robyn J. Hylind, Alexandre C. Pereira, Daniel Quiat, Stephanie F. Chandler, Thomas M. Roston, William T. Pu, Vassilios J. Bezzerides, Jonathan G. Seidman, Christine E. Seidman, Dominic J. Abrams
Publikováno v:
Circ Genom Precis Med
Background: Truncating variants in the desmosomal gene PKP2 (PKP2 tv) cause arrhythmogenic right ventricular cardiomyopathy (ARVC) yet display varied penetrance and expressivity. Methods: We identified individuals with PKP2 tv from the UK Biobank (UK
Autor:
Kurt D. Christensen, Pamela M. McMahon, Lauren N. Galbraith, Jennifer M. Yeh, Natasha K. Stout, Christine Y. Lu, Sarah Stein, Maryann Zhao, Robyn J. Hylind, Ann Chen Wu
Publikováno v:
Genetics in Medicine. 25:100797
Autor:
Robyn J Hylind, Thomas M Roston, Karyn M Austin, Vassilios J Bezzerides, Elizabeth S DeWitt, Dominic J Abrams
Publikováno v:
Circulation. 144
Introduction: Arrhythmogenic cardiomyopathy (ACM) resulting from variants in the desmosomal gene desmoplakin (DSP) is typically an adult onset disorder. Here, we describe penetrance, expression and outcomes of DSP-associated ACM in children. Methods:
Autor:
Vassilios J. Bezzerides, Virginie Beausejour Ladouceur, Andrew J. Powell, Amy E. Roberts, Dominic Abrams, Stephen P. Sanders, Elizabeth S. DeWitt, Christina VanderPluym, Elizabeth D. Blume, Calum A. MacRae, Robyn J. Hylind, Francis Fynn-Thompson, Stephanie F. Chandler, Neal K. Lakdawala
Publikováno v:
J Am Coll Cardiol
BACKGROUND: Arrhythmogenic cardiomyopathy (ACM) is a variably penetrant disease increasingly identified in young patients. OBJECTIVES: This study sought to describe the diverse phenotype, genotype, and outcomes in pediatric and adolescent patients. M