Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Cesar Igor Mesia"'
Autor:
Chi Chi Do‐Nguyen, Maxwell F. Kilcoyne, Randy M. Stevens, James Starc, Nandini Madan, Vicki Mahan, Cesar Igor Mesia, Achintya Moulick
Publikováno v:
Clinical Case Reports, Vol 8, Iss 6, Pp 1034-1038 (2020)
Abstract We describe successful placement of the Inspiris Resilia aortic valve in the pulmonary position. This valve has advantages for immediate benefit and future percutaneous interventions, making it a promising prosthesis for adult congenital pat
Externí odkaz:
https://doaj.org/article/786bf31c074c46718c7ad24f999d3a00
Autor:
Maxwell F. Kilcoyne, James Starc, Nandini Madan, Vicki Mahan, Cesar Igor Mesia, Chi Chi Do-Nguyen, Randy M. Stevens, Achintya Moulick
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 6, Pp 1034-1038 (2020)
Clinical Case Reports, Vol 8, Iss 6, Pp 1034-1038 (2020)
We describe successful placement of the Inspiris Resilia aortic valve in the pulmonary position. This valve has advantages for immediate benefit and future percutaneous interventions, making it a promising prosthesis for adult congenital patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da2c92dff685347601242d6b034eaa3a
https://doi.org/10.1002/ccr3.2794
https://doi.org/10.1002/ccr3.2794
Publikováno v:
World Journal of Cardiovascular Surgery. :29-39
Background: The primary concern of the Fontan procedure has been atrial arrhythmias, but little attention has been given to hemodynamic changes. This study’s purpose was to examine the hemodynamics and arrhythmias of the Intra/extracardiac fenestra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a83a09a9994312265077e38f4828243d
https://doi.org/10.4236/wjcs.2018.82004
https://doi.org/10.4236/wjcs.2018.82004
Autor:
Linda T. Nguyen, Sue Moyer, Rajeev Prasad, Cesar Igor Mesia, Emilee Flynn, Reena Jethva, Rachel Fleishman, Achintya Moulick
Publikováno v:
Clinical Case Reports
Key Clinical Message This case report describes a patient with a 22q11.2 duplication. His features, which include VACTERL association with an esophageal atresia/tracheo‐esophageal fistula and a vascular ring, expand the previously described phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::677336193caf2c4f0129fde6d292ed17
http://europepmc.org/articles/PMC5331229
http://europepmc.org/articles/PMC5331229
Publikováno v:
Journal of cardiac surgery. 34(12)
Background Anomalous left coronary artery (LMCA) arising from the pulmonary artery (ALCAPA) is a life-threatening congenital birth defect. Prompt surgical correction by reimplantation of the LMCA into the aorta is the treatment of choice, however, un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f31d3e93588e16da6d5e4049d7bdcaa
https://pubmed.ncbi.nlm.nih.gov/31638717
https://pubmed.ncbi.nlm.nih.gov/31638717
Publikováno v:
Journal of Clinical Anesthesia. 32:12-16
The internal mammary artery (IMA) has been used as a systemic-to-pulmonary artery shunt in selected patients with congenital heart disease. Growth and development of hypoplastic pulmonary arteries have been described. We discuss the surgical and anes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7dda921f07f4f726f190dc40b26674
https://doi.org/10.1016/j.jclinane.2015.12.017
https://doi.org/10.1016/j.jclinane.2015.12.017
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 6:328-331
A 19-day-old newborn girl weighing 1.9-kg was born with anomalous origin of the left coronary artery (LCA) from the pulmonary artery (PA). Because of the small anatomic structures and long distance between the anomalous origin of the LCA high within
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d30dadc4506b15a09e10e6ee5363df0f
https://doi.org/10.1177/2150135114563768
https://doi.org/10.1177/2150135114563768
Autor:
Shuping Ge, Cesar Igor Mesia, Nicholas Obiri, Jinglan Liu, Carol E. Anderson, Achintya Moulick
Publikováno v:
American Journal of Medical Genetics Part A. 167:268-270
We read with great interest the article by Osoegawa et al. [2014]whichshowedincreasedriskofsexchromosomeaneuploidyamongmales with congenital conotruncal defects. A boy born with trans-position of the great arteries (TGA) was found to have a 47,XXYchr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a78eb45759bd16195fc85d381a21edf
https://doi.org/10.1002/ajmg.a.36814
https://doi.org/10.1002/ajmg.a.36814
Autor:
Ramin Nazari, Jason Parker, Achintya Moulick, Cesar Igor Mesia, Viean Tan, Randy Stevens, Jeffrey J. Cies
Publikováno v:
Critical Care Medicine. 42:A1403
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be17437d1dafd24e823d9beacef63fd1
https://doi.org/10.1097/01.ccm.0000457676.94387.29
https://doi.org/10.1097/01.ccm.0000457676.94387.29
Publikováno v:
Chest. 146:690A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab941a320122fb9a5977284a51ee3cdc
https://doi.org/10.1378/chest.1994742
https://doi.org/10.1378/chest.1994742