Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kimberley A. Myers"'
Publikováno v:
Fluids, Vol 8, Iss 7, p 196 (2023)
Tetralogy of Fallot (TOF) is the most prevalent cyanotic congenital heart defect (CHD) that alters normal blood flow through the heart and accounts for 10% of all CHD. Pulmonary stenosis and regurgitation are common in adults who have undergone TOF r
Externí odkaz:
https://doaj.org/article/1d6fb934f3b649f6b843451366a41e9a
Autor:
Ashifa Hudani, Safia Ihsan Ali, David Patton, Kimberley A. Myers, Nowell M. Fine, James A. White, Steven Greenway, Julio Garcia
Publikováno v:
Applied Sciences, Vol 13, Iss 5, p 2810 (2023)
Patients with Tetralogy of Fallot (TOF) have multiple surgical sequelae altering the pulmonary flow hemodynamics. Repaired TOF (rTOF) adults frequently develop pulmonary regurgitation impacting the blood flow pressure, right ventricle load, and pulmo
Externí odkaz:
https://doaj.org/article/2cc825b777f849a3a27a10e1aee00816
Publikováno v:
Fluids; Volume 8; Issue 7; Pages: 196
Tetralogy of Fallot (TOF) is the most prevalent cyanotic congenital heart defect (CHD) that alters normal blood flow through the heart and accounts for 10% of all CHD. Pulmonary stenosis and regurgitation are common in adults who have undergone TOF r
Autor:
Gary J, Galante, Daryl I, Schantz, Kimberley A, Myers, Charissa R, Pockett, Ivan M, Rebeyka, Andrew S, Mackie
Publikováno v:
Pediatric cardiology. 42(7)
Pericardial effusion (PE) after cardiac surgery can be life threatening without timely detection, and the optimal screening method is unknown. We sought to evaluate the role of a surveillance echocardiogram on postoperative day 10 (± 2), determine t
Autor:
Kimberley A Myers, Michelle Noga, Cinzia Crawley, Edythe B Tham, David J. Patton, Chodchanok Vijarnsorn
Publikováno v:
Pediatric Radiology. 46:991-1002
Standardized methods to evaluate atrial properties in single ventricles are lacking. To determine the feasibility of quantifying right atrial volumes and function in hypoplastic left heart using MRI. We studied 15 infants with hypoplastic left heart
Autor:
Alyssa Power, Nowell M. Fine, David J. Patton, Kimberley A Myers, Jean K. Mah, Sabrina Poonja, Steven C. Greenway, Dal Disler
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 4 (2017)
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine
Background: Advances in medical care for patients with Duchenne muscular dystrophy (DMD) have resulted in improved survival and an increased prevalence of cardiomyopathy. Serial echocardiographic surveillance is recommended to detect early cardiac dy
Autor:
Kimberley A Myers, Frank Dicke, Frederic Dallaire, Steven C. Greenway, Deborah Fruitman, David J. Patton, Robin Clegg, Joyce Harder, Erika E. Vorhies, Yvonne Balon, Tim Prieur, Michael Connelly, Steven R. Martin, Nanette Alvarez, Amyna Fidai, Robert P. Myers
Publikováno v:
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine, Vol 4 (2017)
Frontiers in Cardiovascular Medicine, Vol 4 (2017)
Fontan-associated liver disease (FALD) is a serious complication related to the chronically elevated venous pressure and low cardiac output of this abnormal circulation. However, diagnostic markers for this condition are limited. We hypothesized that
Autor:
Jeffery F. Smallhorn, Edythe B. Tham, Sabira Valiani, Sachie Kaneko, Shelby Kutty, Timothy Colen, Nee S. Khoo, Kimberley A Myers
Publikováno v:
Journal of the American Society of Echocardiography. 27:314-322
Background The long-term prognosis of hypoplastic left heart syndrome is limited by progressive right ventricular dysfunction. The aim of this study was to determine the trends in single right ventricular systolic function between staged palliative s
Publikováno v:
Journal of the American Society of Echocardiography. 26:1221-1227
Background Invasive studies have shown that children with Fontan palliation have abnormal arterial stiffness, impedance, and hydraulic power and efficiency. The aim of this study was to assess these indexes noninvasively in a cohort of children with
Autor:
Lawrence Korngut, Hans D. Katzberg, Basil J. Petrof, Angela Genge, Nicolas Dupré, Julian Raiman, Harvey B. Sarnat, Dubravka Dodig, Mark A. Tarnopolsky, Sandra Sirrs, Kimberley A Myers, Aneal Khan, Shannon L. Venance
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 43(4)
Pompe disease is a lysosomal storage disorder caused by a deficiency of the enzyme acid alpha-glucosidase. Patients have skeletal muscle and respiratory weakness with or without cardiomyopathy. The objective of our review was to systematically evalua