Zobrazeno 1 - 10
of 386
pro vyhledávání: '"Dianna M, Milewicz"'
Autor:
L. Maximilian Buja, MD, Bihong Zhao, MD, PhD, Humaira Sadaf, MD, Michelle McDonald, DO, Ana M. Segura, MD, Li Li, MD, PhD, Alana Cecchi, MS, Siddharth K. Prakash, MD, Rana O. Afifi, MD, Charles C. Miller, PhD, Anthony L. Estrera, MD, Dianna M. Milewicz, MD, PhD
Publikováno v:
Texas Heart Institute Journal, Vol 51, Iss 1, Pp 1-13 (2024)
Objective The purpose of this study was to apply contemporary consensus criteria developed by the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology to the evaluation of aortic pathology, with the expectati
Externí odkaz:
https://doaj.org/article/85a4cbd36f794ae5b7ad2b514235eca3
Autor:
Hector I. Michelena, Alessandro della Corte, Arturo Evangelista, Joseph J. Maleszewski, William D. Edwards, Mary J. Roman, Richard B. Devereux, Borja Fernández, Federico M. Asch, Alex J. Barker, Lilia M. Sierra-Galán, Laurent de Kerchove, Susan M. Fernandes, Paul W.M. Fedak, Evaldas Girdauskas, Victoria Delgado, Suhny Abbara, Emmanuel Lansac, Siddharth K. Prakash, Malenka M. Bissell, Bogdan A. Popescu, Michael D. Hope, Marta Sitges, Vinod H. Thourani, Phillippe Pibarot, Krishnaswamy Chandrasekaran, Patrizio Lancellotti, Michael A. Borger, John K. Forrest, John Webb, Dianna M. Milewicz, Raj Makkar, Martin B. Leon, Stephen P. Sanders, Michael Markl, Victor A. Ferrari, William C. Roberts, Jae-Kwan Song, Philipp Blanke, Charles S. White, Samuel Siu, Lars G. Svensson, Alan C. Braverman, Joseph Bavaria, Thoralf M. Sundt, Gebrine El Khoury, Ruggero de Paulis, Maurice Enriquez-Sarano, Jeroen J. Bax, Catherine M. Otto, Hans-Joachim Schäfers
Publikováno v:
Archivos de Cardiología de México, Vol 94, Iss 2 (2024)
Este consenso de nomenclatura y clasificación para la válvula aórtica bicúspide congénita y su aortopatía está basado en la evidencia y destinado a ser utilizado universalmente por médicos (tanto pediatras como de adultos), médicos ecocardio
Externí odkaz:
https://doaj.org/article/125e7431c8484ba5a45f217644ca1d1c
Autor:
Steven G Carlisle, Hasan Albasha, Hector I Michelena, Anna Sabate-Rotes, Lisa Bianco, Julie De Backer, Laura Muiño Mosquera, Anji T Yetman, Malenka M Bissell, Maria Grazia Andreassi, Ilenia Foffa, Dawn S Hui, Anthony Caffarelli, Yuli Y Kim, Dongchuan Guo, Rodolfo Citro, Margot De Marco, Justin T Tretter, Kim L McBride, Dianna M Milewicz, Simon C Body, Siddharth K Prakash, EBAV Investigators, BAVCon Investigators
Publikováno v:
PLoS ONE, Vol 19, Iss 9, p e0304514 (2024)
Bicuspid aortic valve (BAV), the most common congenital heart defect, is a major cause of aortic valve disease requiring valve interventions and thoracic aortic aneurysms predisposing to acute aortic dissections. The spectrum of BAV ranges from early
Externí odkaz:
https://doaj.org/article/242c32ad450e4d989ceb2ddbfe7c7ae9
Autor:
Suravi Majumder, Abhijnan Chattopadhyay, Jamie M. Wright, Pujun Guan, L. Maximilian Buja, Callie S. Kwartler, Dianna M. Milewicz
Publikováno v:
JCI Insight, Vol 8, Iss 21 (2023)
Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is caused by biallelic loss-of-function variants in pericentrin (PCNT), and premature coronary artery disease (CAD) is a complication of the syndrome. Histopathology of coronary arter
Externí odkaz:
https://doaj.org/article/360d3e60de4c43aebd762e0d1e32e849
Autor:
Sara B. Stephens, Sherene Shalhub, Nicholas Dodd, Jesse Li, Michael Huang, Seitaro Oda, Kalyan Kancherla, Tam T. Doan, Siddharth K. Prakash, Justin D. Weigand, Federico M. Asch, Taylor Beecroft, Alana Cecchi, Teniola Shittu, Liliana Preiss, Scott A. LeMaire, Richard B. Devereux, Reed E. Pyeritz, Kathryn W. Holmes, Mary J. Roman, Ronald V. Lacro, Ralph V. Shohet, Rajesh Krishnamurthy, Kim Eagle, Peter Byers, Dianna M. Milewicz, Shaine A. Morris
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 19 (2023)
Background Arterial tortuosity is associated with adverse events in Marfan and Loeys‐Dietz syndromes but remains understudied in Vascular Ehlers‐Danlos syndrome. Methods and Results Subjects with a pathogenic COL3A1 variant diagnosed at age
Externí odkaz:
https://doaj.org/article/baafb229fe084535a00ef7c97ecf8d3c
Autor:
Louis Saddic, MD, PhD, Amanda Orosco, BS, Dongchuan Guo, PhD, Dianna M. Milewicz, MD, PhD, Dana Troxlair, MD, Richard Vander Heide, MD, David Herrington, MD, Yue Wang, PhD, Ali Azizzadeh, MD, Sarah J. Parker, PhD
Publikováno v:
JVS - Vascular Science, Vol 3, Iss , Pp 85-181 (2022)
Objective: Very few clinical predictors of descending thoracic aorta dissection have been determined. Although aneurysms can dissect in a size-dependent process, most descending dissections will occur without prior enlargement. We compared the proteo
Externí odkaz:
https://doaj.org/article/23a0538677714a06ac21164fdd0831c7
Autor:
Shreyas A. Bhave, Dongchuan Guo, Stoyan N. Angelov, Michael J. Bamshad, Deborah A. Nickerson, Dianna M. Milewicz, Mary C. Wallingford
Publikováno v:
Cardiogenetics, Vol 11, Iss 3, Pp 132-138 (2021)
Thoracic aortic aneurysms (TAAs) that progress to acute thoracic aortic dissections (TADs) are life-threatening vascular events that have been associated with altered transforming growth factor (TGF) β signaling. In addition to TAA, multiple genetic
Externí odkaz:
https://doaj.org/article/ef8c115c55394e3996e080037497968e
Autor:
Krishna R. Ojha, Hyoseon Kim, Samuel Padgham, Laura Hopkins, Robert J. Zamen, Abhijnan Chattopadhyay, Gang Han, Dianna M. Milewicz, Michael P. Massett, Andreea Trache
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 11, p 9616 (2023)
Thoracic aortic aneurysm is found in patients with ACTA2 pathogenic variants. ACTA2 missense variants are associated with impaired aortic smooth muscle cell (SMC) contraction. This study tested the hypothesis that the Acta2R149C/+ variant alters acti
Externí odkaz:
https://doaj.org/article/cb2ac005c9654f7aa408ffa13665c3cb
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 8 (2022)
Externí odkaz:
https://doaj.org/article/90e555481b1c462daee0a12844492e6c
Autor:
John D. Horn, Michael J. Johnson, Zbigniew Starosolski, Avner Meoded, Dianna M. Milewicz, Ananth Annapragada, Shaolie S. Hossain
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Moyamoya disease (MMD) is a progressive steno-occlusive cerebrovascular disease leading to recurrent stroke. There is a lack of reliable biomarkers to identify unilateral stroke MMD patients who are likely to progress to bilateral disease and experie
Externí odkaz:
https://doaj.org/article/c898209b6867446389e42ceb87778dca