Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kemal Ureten"'
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff8908fa5d45bce687b49ea01abfa844
https://doi.org/10.1530/endoabs.49.ep684
https://doi.org/10.1530/endoabs.49.ep684
Autor:
Meral, Calgüneri, Oztürk Meral, Calgüneri, M Akif, Oztürk, Sedat, Kiraz, Ihsan, Ertenli, A Mesut, Onat, Kemal, Ureten, Zeynep, Ozbalkan, Ibrahim C, Haznedaroğlu
Publikováno v:
Joint Bone Spine. 73:334-336
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a95cff93dd6d82b24a5f876d1836bc6
https://doi.org/10.1016/j.jbspin.2005.08.001
https://doi.org/10.1016/j.jbspin.2005.08.001
Autor:
Mevlut, Ceri, Selman, Unverdi, Mustafa, Altay, Kemal, Ureten, M Akif, Oztürk, Namik, Gönen, Murat, Duranay
Publikováno v:
Clinical and experimental rheumatology. 28(4 Suppl 60)
To investigate the prevalence and levels of anti-cyclic citrullinated peptide antibodies (anti-CCP) in patients with familial Mediterranean fever (FMF) with and without arthritis.Eighty-three patients with FMF and 43 healthy controls were included in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6ac300d42a8f354d98bfdc8907fd25d
https://pubmed.ncbi.nlm.nih.gov/20868572
https://pubmed.ncbi.nlm.nih.gov/20868572
Autor:
Kemal, Ureten, Ihsan, Ertenli, M Akif, Oztürk, Sedat, Kiraz, A Mesut, Onat, Murat, Tuncer, Hamza, Okur, Ali, Akdogan, Sule, Apras, Meral, Calgüneri
Publikováno v:
The Journal of rheumatology. 32(5)
Hyperfunction of neutrophils is a characteristic finding in Behçet's disease (BD). Microbial agents have been proposed as causative agents in the disease flares. Fc gamma receptor 1 (CD64) is not normally expressed by neutrophils of healthy individu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e7314bbd0dddc9a0b056f74bfb1d6023
https://pubmed.ncbi.nlm.nih.gov/15868620
https://pubmed.ncbi.nlm.nih.gov/15868620
Autor:
Özlem Karakurt Arıtürk, Kemal Üreten, Münevver Sarı, Nuray Yazıhan, Evin Yılmaz, İmge Ergüder
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 41, Iss 1, Pp 38-44 (2013)
Objectives: Familial Mediterranean fever (FMF) is an autosomal recessive disorder and the most frequent periodic syndrome characterized by recurrent attacks of polyserositis. Heart-type fatty acid-binding protein (h-FABP) is an intracellular molecule
Externí odkaz:
https://doaj.org/article/6c8f887814dd4f86b71d7ef07bcf591f