Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vildan Koşan Çulha"'
Autor:
Tülin Güngör, Özlem Arman Bilir, Vildan Koşan Çulha, Ali Güngör, Abdurrahman Kara, Fatih Mehmet Azık, Hüsniye Neşe Yaralı
Publikováno v:
Pediatrics and Neonatology, Vol 60, Iss 4, Pp 411-416 (2019)
Objective: Immune thrombocytopenic purpura (ITP) is the most common cause of acquired thrombocytopenia children. The aim of this retrospective study is to describe presenting features and clinical characteristics of ITP and evaluate clinical course,
Externí odkaz:
https://doaj.org/article/cca6cb39c8b4425dadee756e260ef5a7
Autor:
Emel Okulu, Talia İleri, Vildan Koşan Çulha, Fatih Mehmet Azık, Yonca Eğin, Zümrüt Uysal, Nejat Akar
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 03, Pp 170-175 (2011)
Objective: To increase our understanding of the etiology of idiopathic thrombocytopenic purpura (ITP) some cytokine gene polymorphisms were analyzed for susceptibility to the disease. The aim of this study was to investigate the role of tumor necrosi
Externí odkaz:
https://doaj.org/article/028383268de642a98609b46822bc60eb
Publikováno v:
Indian Journal of Hematology and Blood Transfusion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::179b224f3092ab1feebd5babdcb5d131
https://doi.org/10.1007/s12288-023-01671-0
https://doi.org/10.1007/s12288-023-01671-0
Autor:
Vildan, Koşan Çulha, Zümrüt, Uysal
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 19(4)
This study evaluated the diagnostic superiority of serum transferrin receptor (sTfR) measurement to other laboratory tests performed for the determination of iron deficiency caused by chronic disease (CD). Study group consisted of 114 anemic patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abebb6d71ce19b6de498ae5d49df840d
https://pubmed.ncbi.nlm.nih.gov/27265186
https://pubmed.ncbi.nlm.nih.gov/27265186
Publikováno v:
The Turkish journal of pediatrics. 55(4)
The aim of this study was to evaluate the causes of thrombocytosis, which was defined as a platelet count greater than 500 x 10(9)/L, and to compare the groups with mild and severe thrombocytosis. A total of 484 patients were evaluated for the etiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::030a49153074c8697af2668681b505a6
https://pubmed.ncbi.nlm.nih.gov/24292035
https://pubmed.ncbi.nlm.nih.gov/24292035
Autor:
Can Alp GENÇ, Dilek GURLEK GOKCEBAY, Vildan KOSAN CULHA, Namık Yasar Ozbek, Yasin KOKSAL, Zühre Kaya
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S21-S22 (2021)
Objective: Prophylaxis treatment is recommended for the prevention of bleeding and complications in patients with hemophilia A. Personalized treatment methods are an up-to-date approach. Hemophilia treatment is suitable for optimization with pharmaco
Externí odkaz:
https://doaj.org/article/f580bfce1c554d82ac5c0977b8438422
Autor:
Fatih Mehmet Azık, Arsen Akıncı, Tülin Revide Şaylı, Vildan Kosan Çulha, Kuddusi Teberik, Mehmet Yasin Teke, Fatih Gürbüz
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 2, Pp 181-184 (2012)
Ocular findings are rarely the initial symptom of leukemia, although up to 90% of all leukemia patients have fundus changes during the course of the disease. Herein we report a relapsing acute lymphoblastic leukemia patient with the sole presentation
Externí odkaz:
https://doaj.org/article/1be26cbcf5534b2495aa4f0e16d421fb