Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Zuhal Demirci"'
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S35-S36 (2023)
Objective: Factor X deficiency (FXd) is a rare coagulation disorder that can be either hereditary or acquired. Case report: We characterized patients with FXd and evaluated their bleeding patterns and treatment strategies. Methodology: This retrospec
Externí odkaz:
https://doaj.org/article/4c866e69714a4f51a189882c56245b96
Publikováno v:
HemaSphere, Vol 7, p e184481b (2023)
Externí odkaz:
https://doaj.org/article/14b5629a3a18408885bff5b87ed3499d
Publikováno v:
HemaSphere, Vol 7, p e38881ba (2023)
Externí odkaz:
https://doaj.org/article/76a0e1fc694946489d2b03ec169dd9c4
Autor:
Kaan Kavaklı, Süha Süreyya Özbek, Ali Bülent Antmen, Fahri Şahin, Şevkiye Selin Aytaç, Alphan Küpesiz, Bülent Zülfikar, Mehmet Sönmez, Ümran Çalışkan, Can Balkan, Tuğana Akbaş, Taner Arpacı, İpek Tamsel, Turgut Seber, Berna Oğuz, Can Çevikol, Mesut Bulakçı, Polat Koşucu, Demet Aydoğdu, İlgen Şaşmaz, Gülen Tüysüz, Başak Koç, Hüseyin Tokgöz, Zuhal Demirci, Burcu Özkan
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 2, Pp 101-110 (2021)
Objective: This study aimed to observe the preventive effect of prophylactic treatment on joint health in people with hemophilia (PwH) and to investigate the importance of integration of ultrasonographic examination into clinical and radiological eva
Externí odkaz:
https://doaj.org/article/ca5ed396cb0a42fea2f11a3b6008d5e6
Akademický článek
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Akademický článek
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Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp 4- (2024)
Objective: FVII deficiency is the most common of the rare congenital bleeding disorders with a prevalence of about 1:500,000. Bleeding symptoms are considerably variable in terms of both location and severity, and may have a heterogenous spectrum ran
Externí odkaz:
https://doaj.org/article/240646efdf574ebb892253f3c0daf8c0
Autor:
Betül Kübra TÜZÜN, Zühal DEMİRCİ, Gülçin ÇELEBİ, Ajda GÜNEŞ, Derya DEMİR, Nur SOYER, Filiz VURAL, Mahmut TÖBÜ, Fahri ŞAHİN, Güray SAYDAM
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp 19-20 (2024)
Objective: Multiple myeloma (MM) is a heterogeneous disease with the uncontrolled clonal proliferation of plasma cells, accounting for approximately 10% of all hematologic cancers . Hence without curative therapy, the treatment aims to improve overal
Externí odkaz:
https://doaj.org/article/baeb06bb15604c1e8476bbfa45a159d5
Autor:
Hatice Demet, Kiper Unal, Melda, Comert Ozkan, Fatos Dilan, Atilla, Zuhal, Demirci, Nur, Soyer, Ilgin, Yildirim Simsir, Ozgur, Omur, Kazim, Capaci, Guray, Saydam, Fahri, Sahin
Publikováno v:
American journal of blood research. 7(5)
Haemophilia has been associated with low bone mineral density (BMD) probably due to some predisposing factors. The aim of this study was to evaluate the relationship between BMD and potential clinical predictors in adult haemophilic patients. Fortyni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8e6336b06fc4abba37593302eb83670
https://pubmed.ncbi.nlm.nih.gov/29181264
https://pubmed.ncbi.nlm.nih.gov/29181264
Publikováno v:
HemaSphere, Vol 7, p e912656b (2023)
Externí odkaz:
https://doaj.org/article/c6554e64877d48d6b61d1fbe0e27c00e