Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gonzalo A. Wallis"'
Autor:
William E. Anderson, Thomas S. Maxey, Matthew C. Schwartz, Aravinth Karunanandaa, Joseph Paolillo, Paul M. Kirshbom, Gonzalo A. Wallis, J. Rene Herlong
Publikováno v:
Cardiology in the Young. 31:1644-1650
Introduction:Systemic ventricular end-diastolic pressure is important in patients with single ventricle heart disease. Predictors of an elevated systemic ventricular end-diastolic pressure prior to bidirectional Glenn operation have been incompletely
Publikováno v:
Pediatric Transplantation. 24
Immunosuppression is necessary after solid organ transplantation. The non-infectious side effects associated with many of these agents are not well understood. We report a case of colitis, most resembling inflammatory bowel disease, that persisted de
Autor:
Jane Gralla, Andrew Savage, Heather T. Henderson, Gonzalo A. Wallis, Richard Kirk, Melanie D. Everitt, Scott R. Auerbach, Karthik Ramakrishnan, Jake A. Kleinmahon, Randall L. Caldwell, Rakesh K. Singh
Publikováno v:
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 38(3)
BACKGROUND Rejection with severe hemodynamic compromise (RSHC) carries a mortality risk approaching 50%. We aimed to identify current risk factors for RSHC and predictors of graft failure after RSHC. METHODS Data from 3,259 heart transplant (HT) reci
Post-cardiotomy mediastinitis is an especially serious complication after the implantation of prosthetic vascular grafts. Standard of care is irrigation, debridement, and removal of all prosthetic material present in the surgical field. The use of an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b9cc55bbe7e0bfbb1b5a0d7a9f9dab7
https://europepmc.org/articles/PMC6260353/
https://europepmc.org/articles/PMC6260353/
Publikováno v:
The Journal of Pediatrics. 162:646-646.e1
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 22 (2011)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Congenitally corrected transposition is a rare cardiac malformation characterized by the combination of discordant atrioventricular and ventriculo-arterial connections, usually accompanied by other cardiovascular malformations. Incidence has been rep