Zobrazeno 1 - 10
of 20
pro vyhledávání: '"David Winlaw"'
Autor:
David M. Kwiatkowski, MD, MS, Jeffrey A. Alten, MD, Kenneth E. Mah, MD, David T. Selewski, MD, Tia T. Raymond, MD, MBA, Natasha S. Afonso, MD, MPH, Joshua J. Blinder, MD, Matthew T. Coghill, MD, David S. Cooper, MD, MPH, Joshua D. Koch, MD, Catherine D. Krawczeski, MD, David L.S. Morales, MD, Tara M. Neumayr, MD, A.K.M. Fazlur Rahman, PhD, Garrett Reichle, MS, Sarah Tabbutt, MD, PhD, Tennille N. Webb, MD, Santiago Borasino, MD, Huaiyu Zang, David Winlaw, MD, David Bailly, DO, Stuart Goldstein, MD, Katja Gist, DO, Katie L. Brandewie, MD, Priya N. Bhat, MD, John W. Diddle, MD, Muhammad Ghbeis, MD, Parthak Prodhan, MD, Xiomara Garcia, MD, Shannon Ramer, Mindy Albertson, Zahidee Rodriquez, MD, Mary Lukacs, Michael Gaies, MD, Joshua Freytag, Amanda Sammons, Hideat Abraha, John Butcher, Dominic Zanaboni, MD, Joan Sanchez de Toledo, MD, PhD, Yuliya A. Domnina, MD, Lucas Saenz, MD, Tracy Baust, Jane Kluck, RN, Jun Sasaki, MD, Aanish Raees, MD, Erika R. O'Neil, MD, Javier J. Lasa, MD, Patrick A. Phillips, Kristal M. Hock, Kevin Valentine, MD, Sachin Tadphale, MBBS, Jason R. Buckley, MD, Luke Schroeder, MD, Shanelle Clarke, MD, Wenying Zhang, MD, Andrew Smith, MD, Mohammed Absi, MD, David J. Askenazi, MD, David J. Askenazi, Parthak Prodhan, Xiomara Garcia, Shanelle Clarke, Zahidee Rodriquez, Muhammad Ghbeis, Jun Sasaki, Katie L. Brandewie, Katja Gist, Michael Gaies, Aanish Raees, Dominic Zanaboni, Joan Sanchez de Toledo, Yuliya A. Domnina, Lucas Saenz, John W. Diddle, Jane Kluck, Linda Duncan, Rebecca A. Bertrandt, Lisa J. Sosa, Priya N. Bhat, Erika R. O’Neal, Javier J. Lasa, Kevin Valentine, Jason R. Buckley, Luke Schroeder, Tammy Doman, Suzanne Viers, Wenying Zhang, Andrew H. Smith, Sachin Tadphale, Mohammed Absi, David K. Bailly
Publikováno v:
JTCVS Open, Vol 19, Iss , Pp 275-295 (2024)
Objective: The study objective was to determine if intraoperative peritoneal catheter placement is associated with improved outcomes in neonates undergoing high-risk cardiac surgery with cardiopulmonary bypass. Methods: This propensity score–matche
Externí odkaz:
https://doaj.org/article/275d57c839a44569916f9a9aa97ba836
Autor:
Erica Tsang, Velda X. Han, Chloe Flutter, Sarah Alshammery, Brooke A. Keating, Tracey Williams, Brian S. Gloss, Mark E. Graham, Nader Aryamanesh, Ignatius Pang, Melanie Wong, David Winlaw, Michael Cardamone, Shekeeb Mohammad, Wendy Gold, Shrujna Patel, Russell C. Dale
Publikováno v:
EBioMedicine, Vol 104, Iss , Pp 105156- (2024)
Summary: Background: Kabuki syndrome (KS) is a genetic disorder caused by DNA mutations in KMT2D, a lysine methyltransferase that methylates histones and other proteins, and therefore modifies chromatin structure and subsequent gene expression. Keton
Externí odkaz:
https://doaj.org/article/706dcecdfb3d41058e9433023d709cb7
Autor:
Rachel Austin, Jaye S. Brown, Sarah Casauria, Evanthia O. Madelli, Tessa Mattiske, Tiffany Boughtwood, Alejandro Metke, Andrew Davis, Ari E. Horton, David Winlaw, Debjani Das, Magdalena Soka, Eleni Giannoulatou, Emma M. Rath, Eric Haan, Gillian M. Blue, Jitendra Vohra, John J. Atherton, Karin van Spaendonck-Zwarts, Kathy Cox, Leslie Burnett, Mathew Wallis, Matilda Haas, Michael C.J. Quinn, Nicholas Pachter, Nicola K. Poplawski, Zornitza Stark, Richard D. Bagnall, Robert G. Weintraub, Sarah-Jane Pantaleo, Sebastian Lunke, Paul De Fazio, Tina Thompson, Paul James, Yuchen Chang, Diane Fatkin, Ivan Macciocca, Jodie Ingles, Sally L. Dunwoodie, Chris Semsarian, Julie McGaughran, Lesley Ades, Annabel Enriquez, Alison McLean, Renee Smyth, Dimithu Alankarage, James McNamara, Morgan almog, Vanessa Fear, Caroline Medi, Mohammad Al-Shinnag, Miriam Fine, Raymond Sy, Keri Finlay, Di Milnes, Dotti Tang, Denisse Garza, Michael Milward, Jessica Taylor, Ansley Morrish, Shelby Taylor, Chris Barnett, Laura Gongolidis, Jim Morwood, Michel Tchan, Belinda Gray, Helen Mountain, Simon Bodek, Cassie Greer, David Mowat, Jordan Thorpe, Kirsten Boggs, Chai-Ann Ng, Alison Trainer, Michael Bogwitz, Mathilda Haas, Natalie Nowak, Gunjan Trivedi, Bernadette Hanna, Noelia Nunez Martinez, Giulia Valente, Alessandra Bray, Richard Harvey, Monique Ohanian, Marie-Jo Brion, Janette Hayward, Sinead O’Sullivan, Jamie Vandenberg, Jaye Brown, Carmen Herrera, Angela Overkov, Kunal Verma, Rob Bryson Richardson, Adam Hill, Miranda Vidgen, Georgie Hollingsworth, Chirag Patel, Charlotte Burns, Georgina Hollway, Mark Perrin, Kathryn Waddel-Smith, Michelle Cao, Matthew Perry, Will Carr, Denise Howting, Andreas Pflaumer, Peta Phillips, Meredith Wilson, Heather Chalinor, Joanne Isbister, Thuan Phuong, Matilda Jackson, Rachel Pope-Couston, Lisa Worgan, Gavin Chapman, Linda Wornham, Theosodia Charitou, Sarah Jane-Pantaleo, Preeti Punni, Kathy Wu, Belinda Chong, Renee Johnson, Laura Yeates, Felicity Collins, Andrew Kelly, Michael Quinn, Dominica Zentner, Gemma Correnti, Sarah King-Smith, Sulekha Rajagopalan, Edwin Kirk, Hariharan Raju, Fiona Cunningham, Sarah Kummerfeld, Timo Lassman, Matthew Regan, Jason Davis, Jonathon Lipton, Jonathan Rogers, Mark Ryan, Sarah Sandaradura, Michelle de Silva, Paul MacIntyre, Nicole Schonrock, Nicola Den Elzen, Paul Scuffham, Sophie Devery, Amali Mallawaarachchi, Julia Dobbins, Julia Mansour, Isabella Sherburn, Ellenore Martin, Mary-Clare Sherlock, Nathan Dwyer, Jacob Mathew, Emma Singer, Stefanie Elbracht-Leong, Carla Smerdon, David Elliott, Janine Smith
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101842- (2024)
Purpose: The Australian Genomics Cardiovascular Disorders Flagship was a national multidisciplinary collaboration. It aimed to investigate the feasibility of genome sequencing (GS) and functional genomics to resolve variants of uncertain significance
Externí odkaz:
https://doaj.org/article/c9654afa9dea4d2db6eb639d8979bf14
Autor:
Samantha J. Lain, Gillian Blue, Bridget O’Malley, David Winlaw, Gary Sholler, Sally Dunwoodie, Natasha Nassar, The Congenital Heart Disease Synergy Study group
Publikováno v:
International Journal of Population Data Science, Vol 8, Iss 1 (2023)
Introduction Contemporary care of congenital heart disease (CHD) is largely standardised, however there is heterogeneity in post-surgical outcomes that may be explained by genetic variation. Data linkage between a CHD biobank and routinely collected
Externí odkaz:
https://doaj.org/article/72ed29d03a0c48cfa50a4406dd639d93
Autor:
Genevieve Coorey, Gemma A. Figtree, David F. Fletcher, Victoria J. Snelson, Stephen Thomas Vernon, David Winlaw, Stuart M. Grieve, Alistair McEwan, Jean Yee Hwa Yang, Pierre Qian, Kieran O’Brien, Jessica Orchard, Jinman Kim, Sanjay Patel, Julie Redfern
Publikováno v:
npj Digital Medicine, Vol 5, Iss 1, Pp 1-12 (2022)
Abstract Potential benefits of precision medicine in cardiovascular disease (CVD) include more accurate phenotyping of individual patients with the same condition or presentation, using multiple clinical, imaging, molecular and other variables to gui
Externí odkaz:
https://doaj.org/article/a89c12ecf5d94282a867fd26e2f2c8ee
Publikováno v:
Genomics, Proteomics & Bioinformatics, Vol 17, Iss 5, Pp 540-545 (2019)
Next-generation sequencing (NGS) technologies generate thousands to millions of genetic variants per sample. Identification of potential disease-causal variants is labor intensive as it relies on filtering using various annotation metrics and conside
Externí odkaz:
https://doaj.org/article/dead9408ef354f299f95d7a34c20e131
Autor:
David Winlaw, Thomas L Gentles, Karin du Plessis, Yves d'Udekem, Johannes Breur, Joelle Julius Nicolaas Daems, Chantal Attard, Suelyn Van Den Helm, Thomas G Wilson
Publikováno v:
Open Heart, Vol 8, Iss 1 (2021)
Background Fontan-associated liver disease is accompanied by a hypercoagulable state. While hepatic dysfunction in Fontan patients is common, its relationship with haemostatic changes and clinical outcomes in this patient population remains unclear.O
Externí odkaz:
https://doaj.org/article/60e1099c73704461b2ebbd89877fa345
Autor:
Brent McSharry, Lahn Straney, Janet Alexander, Tom Gentles, David Winlaw, John Beca, Johnny Millar, Frank Shann, Barry Wilkins, Andrew Numa, Christian Stocker, Simon Erickson, Anthony Slater
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 9 (2019)
Background Outcomes for pediatric cardiac surgery are commonly reported from international databases compiled from voluntary data submissions. Surgical outcomes for all children in a country or region are less commonly reported. We aimed to describe
Externí odkaz:
https://doaj.org/article/5575f7ca28d94d08aeaf0429858ead3e
Publikováno v:
Annals of Pediatric Cardiology, Vol 10, Iss 3, Pp 301-303 (2017)
The anomalous origin of the left brachiocephalic artery in a right sided aortic arch is a rare vascular ring which might lead to esophageal compression. The exact embryological origin of this anomaly is still widely debated. We present an infant who
Externí odkaz:
https://doaj.org/article/8f635c9f9f0448cb94e8d2d97bcdecdb
Autor:
Karina Laohachai, David Winlaw, Hiran Selvadurai, Ganesh Kumar Gnanappa, Yves d'Udekem, David Celermajer, Julian Ayer
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 6, Iss 8 (2017)
BackgroundPatients with a Fontan circulation have reduced exercise capacity and respiratory muscle strength. Inspiratory muscle training (IMT) improves exercise capacity and quality of life in adults with heart failure. We assessed whether 6 weeks of
Externí odkaz:
https://doaj.org/article/84820dbfdc4b4683a6fa11645c95e1db