Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Christine L, D'Arsigny"'
Autor:
Ping Yu Xiong, MD, Zardasht Jaff, MD, Christine L. D’Arsigny, MD, Stephen L. Archer, MD, Don Thiwanka Wijeratne, MD
Publikováno v:
CJC Open, Vol 2, Iss 5, Pp 328-336 (2020)
Background: Although detection of elevated right ventricular systolic pressure (RVSP) on routine echocardiography is common, its clinical significance is underappreciated. The recent change in the hemodynamic definition of pulmonary hypertension (PH)
Externí odkaz:
https://doaj.org/article/0b08c76942a341f7a8310d7d0f8abae0
Autor:
Stefan Edginton, MD, Christine L. D’Arsigny, MD, Cathy McLellan, MD, Stephen L. Archer, MD, FRCP(C), FAHA, FACC
Publikováno v:
CJC Open, Vol 3, Iss 5, Pp 690-692 (2021)
A 51-year-old woman with pulmonary arterial hypertension presented with progressive chest pain and dyspnea. Computed tomography imaging showed significant enlargement of her main pulmonary artery (PA) and was suggestive of left main coronary artery (
Externí odkaz:
https://doaj.org/article/567579c7eed649da95a878409facc6d6
Autor:
Kathryn M. Milne, Matthew D. James, Reginald M. Smyth, Sandra G. Vincent, Namisha Singh, Christine L. D’Arsigny, Juan P. de-Torres, Kerstin de Wit, Amer Johri, J. Alberto Neder, Denis E. O’Donnell, Devin B. Phillips
Publikováno v:
Journal of Applied Physiology. 134:667-677
This study is the first to show that increased exertional dyspnea in patients with post-pulmonary embolism (PE) syndrome, without overt pulmonary hypertension, was strongly associated with elevated inspiratory neural drive (IND) to the diaphragm duri
Autor:
Stephanie R. Sibley, Ian M. Ball, Christine L. D’Arsigny, John W. Drover, Jason W. Erb, Imelda M. Galvin, Daniel W. Howes, Roy Ilan, David W. Messenger, Susan L. Moffatt, Christopher M. Parker, Stacy Ridi, John Muscedere
Publikováno v:
Canadian Journal of Anesthesia/Journal canadien d'anesthésie. 69:1507-1514
Autor:
Kerstin de Wit, Christine L. D’Arsigny
Publikováno v:
Journal of Thrombosis and Haemostasis.
Autor:
Geneviève C Digby, Sean P Keenan, Christopher M Parker, Tasnim Sinuff, Karen E Burns, Sangeeta Mehta, Juan J Ronco, Demetrios J Kutsogiannis, Louise Rose, Najib T Ayas, Luc R Berthiaume, Christine L D’Arsigny, Daniel E Stollery, John Muscedere
Publikováno v:
Canadian Respiratory Journal, Vol 22, Iss 6, Pp 331-340 (2015)
BACKGROUND: The extent of noninvasive ventilation (NIV) use for patients with acute respiratory failure in Canadian hospitals, indications for use and associated outcomes are unknown.
Externí odkaz:
https://doaj.org/article/98aee83615d147a482e5255c77eb24af
Publikováno v:
CJC Open
A 51-year-old woman with pulmonary arterial hypertension presented with progressive chest pain and dyspnea. Computed tomography imaging showed significant enlargement of her main pulmonary artery (PA) and was suggestive of left main coronary artery (
Autor:
Stephanie R, Sibley, Ian M, Ball, Christine L, D'Arsigny, John W, Drover, Jason W, Erb, Imelda M, Galvin, Daniel W, Howes, Roy, Ilan, David W, Messenger, Susan L, Moffatt, Christopher M, Parker, Stacy, Ridi, John, Muscedere
Publikováno v:
Canadian journal of anaesthesia = Journal canadien d'anesthesie. 69(12)
Laryngeal and tracheal injuries are known complications of endotracheal intubation. Endotracheal tubes (ETTs) with subglottic suction devices (SSDs) are commonly used in the critical care setting. There is concern that herniation of tissue into the s
Autor:
William C. Nichols, Anna W. Coleman, Rachel L. Damico, Alexander Hsieh, Brooke Snetsinger, Stephen L. Archer, Lian Tian, Wendy K. Chung, Elina K. Cook, Yufeng Shen, Michael J. Rauh, Paul M. Hassoun, François Potus, Carrie L. Welch, Patricia D.A. Lima, Katie A. Lutz, Michael W. Pauciulo, Jeffrey Mewburn, Christine L. D’Arsigny, Na Zhu, Ashley Martin
Background: Pulmonary arterial hypertension (PAH) is a lethal vasculopathy. Hereditary cases are associated with germline mutations in BMPR2 and 16 other genes; however, these mutations occur in TET2 ), a key enzyme in DNA demethylation, occur in car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b77434d429c8db8dde55ddf0c5992674
https://strathprints.strath.ac.uk/72868/1/Potus_etal_Circulation_2020_Novel_mutations_and_decreased_expression_of_the_epigenetic.pdf
https://strathprints.strath.ac.uk/72868/1/Potus_etal_Circulation_2020_Novel_mutations_and_decreased_expression_of_the_epigenetic.pdf
Autor:
François, Potus, Michael W, Pauciulo, Elina K, Cook, Na, Zhu, Alexander, Hsieh, Carrie L, Welch, Yufeng, Shen, Lian, Tian, Patricia, Lima, Jeffrey, Mewburn, Christine L, D'Arsigny, Katie A, Lutz, Anna W, Coleman, Rachel, Damico, Brooke, Snetsinger, Ashley Y, Martin, Paul M, Hassoun, William C, Nichols, Wendy K, Chung, Michael J, Rauh, Stephen L, Archer
Publikováno v:
Circulation. 141(24)
Pulmonary arterial hypertension (PAH) is a lethal vasculopathy. Hereditary cases are associated with germline mutations inTo test for a role ofWe observed an increased burden of rare, predicted deleterious germline variants inPAH is the first human d