Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Reed, E"'
Autor:
Reed E. Pyeritz, Danielle M. Sienko, Benoit Desjardins, Nicole R. Curnes, Scott O. Trerotola, Jesse Chittams
Publikováno v:
Journal of Vascular and Interventional Radiology. 30:1259-1264
Purpose To assess pulmonary arteriovenous malformation (PAVM) growth among patients with untreated PAVMs using imaging from long-term follow-up per hereditary hemorrhagic telangiectasia international guidelines. Materials and Methods Analysis include
Autor:
Kevin M. Harris, Patrick T. O'Gara, Eric Mittauer, Melinda B. Davis, Eric M. Isselbacher, Lori D. Conklin, Truls Myrmel, Edward P. Chen, Kim A. Eagle, Joseph S. Coselli, Raffi Bekeredjian, Maral Ouzounian, Alan C. Braverman, Stuart Hutchison, Derek R. Brinster, Christina L. Fanola, Dan Gilon, Arturo Evangelista, Toru Suzuki, Reed E. Pyeritz
Publikováno v:
JAMA cardiology. 6(1)
Importance Women with aortopathy conditions are at risk for pregnancy-related aortic dissection, and these conditions may not be recognized until after the aortic dissection occurs. Objective To examine the clinical characteristics, imaging features,
Publikováno v:
Journal of Vascular and Interventional Radiology. 29:981-985
Seven patients with pulmonary arteriovenous malformations (PAVMs) not well suited to coil and/or plug treatment were treated with expanded polytetrafluoroethylene-covered stents. Mean diameter of treated arteries was 6 mm. Complete technical success
Autor:
Stephanie Burns Wechsler, Arvind Hoskoppal, Wyman W. Lai, Luciana Young, Reed E. Pyeritz, Ronald V. Lacro, Timothy J. Bradley, Kristin M. Burns, Jami C. Levine, Aimee Liou, Bruce D. Gelb, Julie De Backer, Felicia Trachtenberg, Angela M. Sharkey, Marie L. Gleason, Elif Seda Selamet Tierney, Lynn Mahony, Aaron K Olson, Jeanne James, Mario Stylianou, Shaji C. Menon
Publikováno v:
Pediatric cardiology, 39(7), 1453-1461. Springer New York
Few data exist regarding predictors of rapid aortic root dilation and referral for aortic surgery in Marfan syndrome (MFS). To identify independent predictors of the rate of aortic root (AoR) dilation and referral for aortic surgery, we investigated
Autor:
M. Elizabeth Brickner, Reed E. Pyeritz, Kathryn C. Chatfield, Dianna M. Milewicz, Anthony L. Estrera, Ellen S. Regalado, Hiroko Morisaki, Patricia L. Musolino, Lauren Mellor-Crummey, Susan L. Benedict, Mustafa Tekin, Denver Sallee, Kathryn W. Holmes, Timothy J. Bradley, Cori Feist, Glen J. Iannucci, Julie Richer, Sherene Shalhub, John R. Østergaard, Lesley C. Adès, Anne H. Child, Paul R. Mark, Shaine A. Morris, Anna L. Mitchell, Birgit Lorenz, Julie De Backer, Takayuki Morisaki, Anji T. Yetman, Alan C. Braverman
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Regalado, E S, Mellor-Crummey, L, De Backer, J, Braverman, A C, Ades, L, Benedict, S, Bradley, T J, Brickner, M E, Chatfield, K C, Child, A, Feist, C, Holmes, K W, Iannucci, G, Lorenz, B, Mark, P, Morisaki, T, Morisaki, H, Morris, S A, Mitchell, A L, Ostergaard, J R, Richer, J, Sallee, D, Shalhub, S, Tekin, M, Estrera, A, Musolino, P, Yetman, A, Pyeritz, R, Milewicz, D M & Montalcino Aortic Consortium 2018, ' Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations ', Genetics in Medicine, vol. 20, no. 10, pp. 1206-1215 . https://doi.org/10.1038/gim.2017.245
Regalado, E S, Mellor-Crummey, L, De Backer, J, Braverman, A C, Ades, L, Benedict, S, Bradley, T J, Brickner, M E, Chatfield, K C, Child, A, Feist, C, Holmes, K W, Iannucci, G, Lorenz, B, Mark, P, Morisaki, T, Morisaki, H, Morris, S A, Mitchell, A L, Ostergaard, J R, Richer, J, Sallee, D, Shalhub, S, Tekin, M, Estrera, A, Musolino, P, Yetman, A, Pyeritz, R, Milewicz, D M & Montalcino Aortic Consortium 2018, ' Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations ', Genetics in Medicine, vol. 20, no. 10, pp. 1206-1215 . https://doi.org/10.1038/gim.2017.245
Purpose: Smooth muscle dysfunction syndrome (SMDS) due to heterozygous ACTA2 arginine 179 alterations is characterized by patent ductus arteriosus, vasculopathy (aneurysm and occlusive lesions), pulmonary arterial hypertension, and other complication
Autor:
Daniel G. Montgomery, Kim A. Eagle, Udo Sechtem, Marco Di Eusanio, Guillaume Jondeau, Marc P. Bonaca, Christoph A. Nienaber, James B. Froehlich, Eduardo Bassone, Fabio Ramponi, Himanshu J. Patel, Mohammad Abbasi, Eric M. Isselbacher, Hans-Henning Eckstein, Mark E. Lindsay, Reed E. Pyeritz, Ali Khoynezhad
Publikováno v:
Circulation. 134:1013-1024
Background: Improved medical care after initial aortic dissection (AD) has led to increased survivorship and a population of individuals at risk for further cardiovascular events, including recurrent AD. Reports describing recurrent ADs have been res
Autor:
Alexander P. Nissen, Van Thi Thanh Truong, Bader A. Alhafez, Jyothy J. Puthumana, Anthony L. Estrera, Simon C. Body, Siddharth K. Prakash, Eduardo Bossone, Rodolfo Citro, Simon Body, J. Daniel Muehlschlegel, Jasmine T. Shahram, Thy B. Nguyen, Vicenza Stefano Nistri, Dan Gilon, Ronen Durst, Carlo de Vincentiis, Francesca R. Pluchinotta, Thoralf M. Sundt, Hector I. Michelena, Giuseppe Limongelli, Patrick M. McCarthy, S. Chris Malaisrie, Aakash Bavishi, Malenka M. Bissell, Gordon S. Huggins, Victor Dayan, Francois Dagenais, Alessandro Della Corte, Evaldas Girdsaukas, Bo Yang, Kim Eagle, Dianna M. Milewicz, Tom C. Nguyen, Harleen K. Sandhu, Hazim J. Safi, Josh C. Denny, Arturo Evangelista, Laura Galian-Gay, Kim A. Eagle, Williams Ravekes, Harry C. Dietz, Kathryn W. Holmes, Jennifer Habashi, Scott A. LeMaire, Joseph S. Coselli, Shaine A. Morris, Cheryl L. Maslen, Howard K. Song, G. Michael Silberbach, Reed E. Pyeritz, Joseph E. Bavaria, Karianna Milewski, Richard B. Devereux, Jonathan W. Weinsaft, Mary J. Roman, Ralph V. Shohet, Nazli McDonnell, Federico M. Asch, H. Eser Tolunay, Patrice Desvigne-Nickens, Hung Tseng, Barbara L. Kroner
Publikováno v:
The Journal of thoracic and cardiovascular surgery. 159(6)
Objective: Bicuspid aortic valve is a common risk factor for thoracic aortic aneurysm and dissection. Guidelines for elective ascending aortic intervention (AAI) in bicuspid aortic valve are derived from limited evidence, and the extent of practice v
Autor:
Roman, Mary J., Pugh, Norma L., Devereux, Richard B., Eagle, Kim A., Holmes, Kathryn, LeMaire, Scott A., Milewski, Rita K., Morris, Shaine A., Prakash, Siddharth K., Pyeritz, Reed E., Ravekes, William J., Shohet, Ralph V., Song, Howard K., Asch, Federico M.
This study analyzed the impact of sex, hemodynamic profile, and valve fusion pattern on aortopathy associated with bicuspid aortic valve (BAV). The National Heart Lung and Blood Institute-sponsored National Registry of Genetically Triggered Thoracic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98b9efebeb93dd612f6b40297f945090
https://europepmc.org/articles/PMC5593782/
https://europepmc.org/articles/PMC5593782/
Autor:
Joseph M, Krepp, Mary J, Roman, Richard B, Devereux, Adrienne, Bruce, Siddharth K, Prakash, Shaine A, Morris, Dianna M, Milewicz, Kathryn W, Holmes, William, Ravekes, Ralph V, Shohet, Reed E, Pyeritz, Cheryl L, Maslen, Barbara L, Kroner, Kim A, Eagle, Liliana, Preiss, Federico M, Asch
Publikováno v:
Congenital heart disease. 12(6)
Background Unicuspid aortic valve (UAV) is a rare disorder, often difficult to distinguish from bicuspid aortic valve (BAV). BAV and UAV share valve pathology such as the presence of a raphe, leaflet fusion, aortic stenosis, aortic regurgitation, and
Publikováno v:
Cardiovascular and interventional radiology. 40(7)
To determine current practice regarding screening, management, and follow-up of pulmonary arteriovenous malformations (PAVMs), particularly those with feeding arteries