Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Makram R. Ebeid"'
Autor:
Sarosh P Batlivala, Makram R Ebeid
Publikováno v:
Annals of Pediatric Cardiology, Vol 12, Iss 1, Pp 60-63 (2019)
Fontan completion in patients with complex cardiac anatomy, and specifically heterotaxy syndrome, can present unique physiologic considerations. For example, existing venous connections may be “unmasked” after a cavopulmonary anastomosis operatio
Externí odkaz:
https://doaj.org/article/a52752c7906946c0b28d3dc2c63ce0f6
Publikováno v:
Annals of Pediatric Cardiology, Vol 11, Iss 2, Pp 181-186 (2018)
Systemic-to-pulmonary artery collateral networks commonly develop in patients with single-ventricle physiology and chronic hypoxemia. Although these networks augment pulmonary blood flow, much of the flow is ineffective and contributes to cardiac vol
Externí odkaz:
https://doaj.org/article/f501b9a20bc54738a603b0cc51fab019
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 44, Iss 4, Pp 346-349 (2016)
Summary– While trisomy 21 is a common genetic disorder in singletons, the incidence among identical twins is very rare, occurring in approximately 1–2 per 1000 twin gestations. Trisomy 21 is associated with high incidence of congenital heart defe
Externí odkaz:
https://doaj.org/article/85d8053e270b40ccb14683789c0ba14e
Autor:
Oliver G. Abela, George S. Abela, Amer Alaiti, Mazen S. Albaghdadi, Carlos E. Alfonso, Hilary F. Armstrong, Steven R. Bailey, Subhash Banerjee, Ori Belson, Navid Berenji, Gary N. Binyamin, Joao Braghiroli, Emmanouil S. Brilakis, Shmuel Chen, Michael Clifton, Jose F. Condado, Jennifer P. Connell, Michael Dangl, Kathryn Das, Makram R. Ebeid, Gabby Elbaz-Greener, Matthew C. Evans, Alexandre Ferreira, Aloke V. Finn, Nathan Frogge, Offer Galili, Samantha Gaston, Jessica Nathalia González, K. Jane Grande-Allen, Jelani K. Grant, Aashish Gupta, null Adrian Howansky, Dora Y. Huang, Kurt Jacobson, J. Stephen Jenkins, Thomas Johnson, Gregory K. Jones, Elysa Jui, Edo Kaluski, Vasili Katsadouros, Sameer Khandhar, Eitan Konstantino, Maya Konstantino, Alexandra Lansky, John Lasala, Neil Pendril Lewis, Alejandro Eric Macias, Michael Magarakis, Mark Mariathas, Cesar E. Mendoza, Ryan Merritt, Hayley Moore, Masayuki Mori, John Moscona, William B. Moskowitz, Liam Musto, Hoang Nguyen, Odunayo Olorunfemi, Takayuki Onishi, Yuko Onishi, Peter O'Kane, Purven Parikh, Samuel P. Powell, Marloe Prince, Furqan A. Rajput, Sarah Reeves, Prakash Saha, Tomas Antonio Salerno, Yu Sato, Megan Sattler, Sudhakar Sattur, Amit Shah, Nicolas W. Shammas, Venkat Shankarraman, Reema Sheth, Kavya L. Singampalli, Dilpreet Singh, George A. Stouffer, Bradley H. Strauss, Christopher B. Sylvester, Prashanth Thakker, Manoj Thangam, Thomas M. Todoran, Catalin Toma, On Topaz, Nirupama Vellanki, Renu Virmani, Xin Wei, Giora Weisz, Christopher J. White, Scott L. Willis, Iosif Xenogiannis, Jeffrey P. Yourshaw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60ac8db936ae08297ff56387b36ed4f0
https://doi.org/10.1016/b978-0-12-821451-0.01002-8
https://doi.org/10.1016/b978-0-12-821451-0.01002-8
Autor:
Makram R. Ebeid, Sarosh P. Batlivala
Publikováno v:
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology, Vol 12, Iss 1, Pp 60-63 (2019)
Annals of Pediatric Cardiology, Vol 12, Iss 1, Pp 60-63 (2019)
Fontan completion in patients with complex cardiac anatomy, and specifically heterotaxy syndrome, can present unique physiologic considerations. For example, existing venous connections may be "unmasked" after a cavopulmonary anastomosis operation. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d2f35a21ccc77077bd687acac76f9d3
http://europepmc.org/articles/PMC6343381
http://europepmc.org/articles/PMC6343381
Autor:
Makram R. Ebeid, Jannika Dodge-Khatami, Ali Dodge-Khatami, Jorge D. Salazar, Mary B. Taylor, Divya Shakti, Mary K Hood, Sarosh P. Batlivala
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 9:68-73
Background: Traditional palliation for biventricular cyanotic congenital heart lesions often involves staging with systemic-to-pulmonary arterial shunts to secure pulmonary blood flow (PBF) in the newborn period prior to complete repair. However, shu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9216b68ed90e662cef30987e77f5ea37
https://doi.org/10.1177/2150135117738007
https://doi.org/10.1177/2150135117738007
Autor:
Wolfgang Radtke, Makram R. Ebeid, Ralf J. Holzer, Daniel H. Gruenstein, Phillip Moore, Henri Justino
Publikováno v:
Catheterization and Cardiovascular Interventions. 89:1118-1128
Objectives The study purpose is to evaluate the safety and efficacy of the ADO II device for closure of patent ductus arteriosus (PDA) in children. Background Transcatheter treatment of PDA has been evolving for 40+ years and is the treatment of choi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afe52d9c143bc93e90a66f3ddd1724de
https://doi.org/10.1002/ccd.26968
https://doi.org/10.1002/ccd.26968
Autor:
Caroline Michot, Julie D. Kaplan, G. Paul Matherne, Makram R. Ebeid, Barrett H. Barnes, Elaine H. Zackai, Mark E. Lindsay, Matthew J. O'Connor, Thomas J. L'Ecuyer, Angela E. Lin, Elizabeth Krieg, Andrew C. Edmondson, Joel B. Krier, Brian B. Ghoshhajra, Valérie Cormier-Daire, Jennifer B. Humberson
Publikováno v:
American Journal of Medical Genetics Part A. 170:2617-2631
Myhre syndrome is a rare, distinctive syndrome due to specific gain-of-function mutations in SMAD4. The characteristic phenotype includes short stature, dysmorphic facial features, hearing loss, laryngotracheal anomalies, arthropathy, radiographic de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::961d86919f441d94cc6960e99d720ca7
https://doi.org/10.1002/ajmg.a.37739
https://doi.org/10.1002/ajmg.a.37739
Publikováno v:
Annals of Pediatric Cardiology, Vol 11, Iss 2, Pp 181-186 (2018)
Systemic-to-pulmonary artery collateral networks commonly develop in patients with single-ventricle physiology and chronic hypoxemia. Although these networks augment pulmonary blood flow, much of the flow is ineffective and contributes to cardiac vol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3bd605965465cd4a9dbfb0e979f6a2b
https://pubmed.ncbi.nlm.nih.gov/29922015
https://pubmed.ncbi.nlm.nih.gov/29922015
Autor:
Charles H. Gaymes, Makram R. Ebeid
Publikováno v:
Catheterization and Cardiovascular Interventions. 82:E688-E693
Bidirectional Glenn shunt is usually performed in patients with single ventricle in preparation for a total cavo-pulmonary connection. We present a patient born with complex congenital heart disease consisting of single ventricle, pulmonary atresia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0f82cfde03681ec135bb021a291d631
https://doi.org/10.1002/ccd.23142
https://doi.org/10.1002/ccd.23142