Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mehmet Dikec"'
Autor:
Abdulmecit Yildiz, Sena Ulu, Aysegul Oruc, Ali Riza Ucar, Savas Ozturk, Selma Alagoz, Necmi Eren, Ismail Kocyigit, Simal Koksal Cevher, Ali Burak Haras, Abdullah Sumnu, Turgay Arinsoy, Garip Sahin, Gultekin Suleymanlar, Caner Cavdar, Gizem Kumru Sahin, Ilhan Kurultak, Abdulkadir Unsal, Gulizar Sahin, Sinan Kazan, Erhan Tatar, Mehmet Dıkec, Belda Dursun, Hayriye Sayarlioglu, Kultigin Turkmen, Ayse Serra Artan, Nimet Aktas, Zulfikar Yilmaz, Ahmet Behlul, Hamad Dheir, Sim Kutlay, Nurhan Seyahi
Publikováno v:
Renal Failure, Vol 44, Iss 1, Pp 1048-1059 (2022)
Background We aimed to evaluate the features of primary membranous nephropathy (MNP) in Turkish people.Methods This is a retrospective analysis of patients with biopsy-proven primary MNP. We obtained the data collected between 2009 and 2019 in the pr
Externí odkaz:
https://doaj.org/article/c36df02bb08a47bfa7a3a1c02a6b3880
Autor:
Gunden Deger, Mahmut Nezih Carin, Zeki Toprak, Umut Kasapoğlu, Arzu Ozdemir Kayalar, Fatih Gokhan Akbay, Suheyla Apaydin, Mehmet Dikec, Aysegul Kudu
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims The recipients who have antibodies againts to donors’ HLA (Anti HLA- DSA) carrie a huge risk for allograf (AG) losing. In current study, it was retrospectively evaluated whether the live donor kidney recipients (LDKRs) under des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52d19478aabab3ee65f270eb3a12fec9
https://doi.org/10.1093/ndt/gfaa142.p1787
https://doi.org/10.1093/ndt/gfaa142.p1787
Autor:
Necmi Eren, Turgay Arinsoy, Ali Burak Haras, Abdulmecit Yildiz, Garip Sahin, Ismail Koçyiğit, Mehmet Dikec, Zulfikar Yilmaz, Savas Ozturk, Abdullah Sumnu, Ahmet Behlul, Ayse Serra Artan, Gizem Kumru Gahin, Memnune Sena Ulu, Nimet Aktas, Abdulkadir Unsal, Sim Kutlay, Bulent Vatansever, Hamad Dheir, Gulizar Manga Sahin, Ali Riza Ucar, Ilhan Kurultak, Hayriye Sayarlioğlu, Şimal Köksal Cevher, Aysegul Oruc, Selma Alagoz, Caner Çavdar, Gultekin Suleymanlar, Nurhan Seyahi, Sinan Kazan, Kultiin Turkmen, Belda Dursun
Publikováno v:
Nephrology Dialysis Transplantation. 35
Background and Aims Membranous nephropathy (MN) is the most common cause of nephrotic syndrome in the adult population. The aim of our study is to determine the demographic and clinical characteristics and biopsy findings of the patients diagnosed wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::813f7130d49c4839deddc96eeb7c7c5a
https://doi.org/10.1093/ndt/gfaa142.p0425
https://doi.org/10.1093/ndt/gfaa142.p0425
Autor:
Sheyla Apaydin, Murat Tuğcu, Gülbüz Sezgin, Mehmet Dikec, Gulizar Manga Sahin, Mustafa Canbakan, Murat Gücün, Aysun Yakut
Publikováno v:
Genomics. 43:115-122
Alkaptonuria (AKU; McKusick No. 203500), a rare hereditary disorder of the phenylalanine catabolism, was the first disease to be interpreted as an inborn error of metabolism (A. E. Garrod, 1902, Lancet 2: 1616-1620). AKU patients are deficient for ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcfa5bdb0322ed88a2e8d54cd2fac06e
https://doi.org/10.1006/geno.1997.4805
https://doi.org/10.1006/geno.1997.4805