Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kamil Kilic"'
Autor:
Murat Kilic, Rasim Farajov, Zaza Iakobadze, Seray Akcalar, Dilsat Camli, Kamil Kilic, Cahit Yilmaz, Can A. Karaca
Publikováno v:
Transplantation Proceedings. 55:375-378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8962e33e441b74c035903643dcfb7a04
https://doi.org/10.1016/j.transproceed.2023.02.008
https://doi.org/10.1016/j.transproceed.2023.02.008
Autor:
Kamil Kilic, Gokhan Temiz, Murat Zeytunlu, Murat Kilic, Mehmet Alper Kamil Kilic, Mehmet Alper
Publikováno v:
Archives of Clinical and Experimental Surgery, Vol 4, Iss 3, Pp 135-141 (2015)
Objective: Liver transplantation has been one of the areas in which microvascular surgery is frequently practiced. With the use of microsurgical techniques in hepatic artery anastomosis, the incidence of hepatic artery thrombosis has been signifi- ca
Externí odkaz:
https://doaj.org/article/ab3bd796f2a149018fdd3ff2c00a6bee
Autor:
Kamil Kilic, Cahit Yilmaz, Sema Aydogdu, Rasim Farajov, Murat Kilic, Zaza Iakobadze, Can Karaca
Publikováno v:
Liver Transplantation. 27:257-263
Biliary complications (BCs) are still a major cause of morbidity following liver transplantation despite the advancements in the surgical technique. Although Roux-en-Y (RY) hepaticojejunostomy has been the standard technique for years in pediatric pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3538e1925fd0fa6cc3cbc43b833ae7b1
https://doi.org/10.1002/lt.25845
https://doi.org/10.1002/lt.25845
Autor:
Can Karaca, Suat Buket, Rasim Farajov, Zaza Iakobadze, Murat Kilic, Kamil Kilic, Cahit Yilmaz
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation.
Objectives Living-donor liver transplant for BuddChiari syndrome is particularly challenging because of the need for venous outflow reconstruction as grafts from living donors lack vena cava. In addition, recipient vena cava may be thrombotic and fib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::766245e0a57aa2140db8bd5e25bbf7e2
https://pubmed.ncbi.nlm.nih.gov/31801445
https://pubmed.ncbi.nlm.nih.gov/31801445
Autor:
Kamil Kilic, Rasim Ferecov, Adnan Tosun, Can A. Karaca, Murat Kilic, Zaza Iakobadze, Cahit Yilmaz
Publikováno v:
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society. 24(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf12f4ab345eb533c2a2ead5aaec3398
https://pubmed.ncbi.nlm.nih.gov/29108119
https://pubmed.ncbi.nlm.nih.gov/29108119
Publikováno v:
Journal of Craniofacial Surgery. 15:222-225
Benign osteoblastoma is a rare primary bone tumor that constitutes approximately 1% of all primary bone tumors. Its occurrence in the craniomaxillofacial region as also rare and represents only 15% of all osteoblastomas. The tumor shows a predilectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f385c938356b19741ff34fe4b9b9792c
https://doi.org/10.1097/00001665-200403000-00009
https://doi.org/10.1097/00001665-200403000-00009
Akademický článek
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Publikováno v:
The Journal of craniofacial surgery. 15(3)
Gardner syndrome, a variant of familial adenomatous polyposis, is an autosomal dominant disease characterized by gastrointestinal polyps that develop in the colon as well as in the stomach and upper intestine (duodenum), multiple osteomas, and skin a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3c494b83d27eebdc8b316d13e58d651
https://pubmed.ncbi.nlm.nih.gov/15111819
https://pubmed.ncbi.nlm.nih.gov/15111819
