Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Reed, E."'
Autor:
Daniel M. DePietro, Reed E. Pyeritz, Jesse Chittams, Scott O. Trerotola, Nicole R. Curnes, Victor A. Ferrari
Publikováno v:
Chest. 157:1278-1286
Background High-resolution chest CT (HRCT) scan is recommended after pulmonary arteriovenous malformation (PAVM) embolotherapy to assess for PAVM persistence and untreated PAVM growth. Graded transthoracic contrast echocardiography (TTCE) predicts th
Autor:
Mary J. Roman, Reed E. Pyeritz, Kim A. Eagle, Sherene Shalhub, Gabriele Di Luozzo, Erin R Lewis, Tracy Andrews, Scott A. LeMaire, Federico M. Asch
Publikováno v:
Circulation. 142
Objective: Evaluating progression of distal aortopathy among patients with GT-TAA. Methods: 1,160 patients (2007-2014) including 226 patients with >=2 CT/MRI scans; mean surveillance=1.5±1.4 years. Rapid progression (RP) was within the fourth quar
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,
Autor:
Davide Pacini, Marc Shermerhorn, Santi Trimarchi, Kim A. Eagle, Truls Myrmel, Raffi Bekeredjian, Marek P. Erlich, Reed E. Pyeritz, Chiara Lomazzi, Alan C. Braverman
Acute aortic dissection (AAD) is a life-threatening disorder that is challenging to diagnose and with defined optimal therapies and outcomes. It is associated with high morbidity and mortality rates, in spite of new management approaches developed ov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88661365ca56e3bca40fc1892608fef1
http://hdl.handle.net/11585/807202
http://hdl.handle.net/11585/807202
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:
Jami C. Levine, David A. Parra, Julie De Backer, Elif Seda Selamet Tierney, Arni Nutting, Reed E Pyeritz, Meryl S. Cohen, Gail D. Pearson, Aimee Liou, Shubhika Srivastava, Timothy J. Bradley, Steven D. Colan, Angela M. Sharkey, Aaron K Olson, Shan Chen, Arvind Hoskoppal, M. Jay Campbell, Edward Marcus, Haleh Heydarian, Mary Ella M Pierpont, William Ravekes, Lynn A. Sleeper, Luciana Young, Ronald V. Lacro, Mary J. Roman, Wyman W. Lai, Beth F. Printz
Publikováno v:
The American Journal of Cardiology. 121:1094-1101
The Pediatric Heart Network randomized trial of atenolol versus losartan in the Marfan syndrome showed no treatment differences in the rates of aortic-root growth or clinical outcomes. In this report we present treatment effects on aortic stiffness a
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:
K. A. Eagle, Dianna M. Milewicz, Kalyan Kancheria, Seitaro Oda, Taylor Beecroft, Liliana Preiss, Federico M. Asch, Rajesh Krishnamurthy, Justin P. Zachariah, Kathryn W. Holmes, Tam Doan, Teniola Shittu, Sherene Shalhub, Shaine A. Morris, Ralph V. Shohet, Nicholas A. Dodd, M.J. Roman, Scott A. LeMaire, Ronald V. Lacro, Peter H. Byers, Richard Devereux, Sara Stephens, Alana Cecchi, Justin Weigand, Reed E. Pyeritz
Publikováno v:
Journal of the American College of Cardiology. 75:1621
Vertebral artery tortuosity has been associated with adverse events in Marfan and Loeys-Dietz syndromes, but has not been assessed in Vascular Ehlers-Danlos syndrome (VEDS). Subjects
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
Autor:
Daniel G. Montgomery, Linda Pape, Kim A. Eagle, Reed E. Pyeritz, Kevin M. Harris, Eduardo Bossone, Thomas T. Tsai, Christoph A. Nienaber, Mark J. Russo, Alan C. Braverman, G. Chad Hughes, Eric M. Isselbacher, Patrick T. O'Gara
Publikováno v:
The American Journal of Medicine. 126:909-915
Few data exist on race-related differences in acute aortic dissection patients.We evaluated black (n = 189, 14%) or white (n = 1165, 86%) patients (mean age 62.8 ± 15.3 years; 36.4% women) enrolled in 13 US centers participating in the International