Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yucel, Yankol"'
Autor:
Yucel Yankol, Nesimi Mecit, Turan Kanmaz, Gokhan Ertugrul, Koray Acarli, Munci Kalayoglu, Hale Kirimlioglu
Publikováno v:
Experimental and Clinical Transplantation. 20:104-107
Smith-Lemli-Opitz syndrome is an autosomal recessive metabolic disease characterized by mental retardation and multiple congenital anomalies. The main pathology is the lack of the enzyme 3β-hydroxysterol Δ7-reductase, which is the last enzymatic st
Autor:
Margorit Rita Krespi, Asli Tankurt, Koray Acarlı, Yucel Yankol, Munci Kalayoglu, Turan Kanmaz
Publikováno v:
Cogent Psychology, Vol 3, Iss 1 (2016)
Aim: Liver transplantation from living donors affects not only recipients’ but also donors’ lives. The aim of this study was to explore living donors’ experience of life. Methods: The sample consisted of 16 living donors who donated a part of t
Externí odkaz:
https://doaj.org/article/08060938e5a14bdfb7d68ddd5573784a
Publikováno v:
American Journal of Transplantation. 20:611-613
Autor:
Emily Bugeaud, Anthony M. D'Alessandro, David P. Foley, Yucel Yankol, Michael D. Rizzari, Tiffany Zens, Koray Acarli, Oya Andacoglu, Glen Leverson, Nesimi Mecit, Joshua D. Mezrich, Munci Kalayoglu, Turan Kanmaz, Luis A. Fernandez
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim: the progression of chronic kidney disease (CKD) in recipients of living-donor liver transplant (LDLT) compared to deceased-donor liver transplant (DDLT) has not been studied in the literature. We hypothesize that CKD stage progression
Autor:
Tiffany Zens, Anthony M. D’Alessandro, Michael J. Eerhart, Peter J. Chlebeck, Jose A. Reyes, Saverio Capuano, Daniel Burguete, Yucel Yankol, Yolanda Ponstein, Luis A. Fernandez, Jose R. Torrealba, Jennifer Coonen, William J. Burlingham, Kevin Brunner, Laura J. Zitur, Edwin Van Amersfoort, Myron A. Pozniak, Jeremy A. Sullivan, Juan S. Danobeitia, Arjang Djamali, Ewa Jankowska-Gan, Cees van Kooten
Publikováno v:
American Journal of Transplantation, 20(6), 1513-1526. WILEY
Delayed graft function (DGF) in renal transplant is associated with reduced graft survival and increased immunogenicity. The complement-driven inflammatory response after brain death (BD) and posttransplant reperfusion injury play significant roles i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b7a7a020e6c0b5601705b12f0a6b72
https://hdl.handle.net/1887/3185005
https://hdl.handle.net/1887/3185005
Publikováno v:
Turk J Surg
Turkish Journal of Surgery
Turkish Journal of Surgery
Objective: living liver donor surgery is a major surgical procedure applied to healthy people with mortality and morbidity risks and does not provide any direct therapeutic advantage to the donor. We retrospectively analyzed the postoperative complic
Autor:
Tevfik, Küçükkartallar1 tevfikkk75@hotmail.com, Yucel, Yankol1, Turan, Kanmaz1, Serdar, Topaloğlu1, Koray, Acarli1, Munci, Kalayoglu1
Publikováno v:
Pediatric Transplantation. May2011, Vol. 15 Issue 3, p281-284. 4p. 4 Charts.
Autor:
Yucel Yankol
Publikováno v:
Hepatology. 58:776A-785A
Autor:
Yucel, Yankol, Mustafa, Ertugrul, Turan, Kanmaz, Nesimi, Mecit, Ilhan, Ocak, Ozlem, Durmaz, Koray, Acarli, Munci, Kalayoglu
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 14(5)
Acute liver failure is a rapidly progressive and life-threatening disease in children, whose clinical features differ from those of adults.This is a review of a single center's experience with pediatric acute liver failure in a region with insufficie
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 15(5)
Argininosuccinic aciduria is a urea cycle disorder caused by an argininosuccinate lyase enzyme deficiency that ends with nitrogen accumulation as ammonia. Argininosuccinic aciduria patients are at risk for long-term complications including poor neuro