Zobrazeno 1 - 10
of 174
pro vyhledávání: '"Fahri Şahin"'
Autor:
Elif Gülsüm Ümit, Ahmet Muzaffer Demir, Muhlis Cem Ar, Mesut Ayer, Meltem Aylı, Volkan Karakuş, Emin Kaya, Fahir Özkalemkaş, Nilgün Sayınalp, Mehmet Sönmez, Fahri Şahin, Selami Koçak Toprak, Tayfur Toptaş, İrfan Yavaşoğlu, Ümran Çalış
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 3, Pp 141-145 (2024)
Objective: Primary immune thrombocytopenia (ITP) is an acquired disorder of platelets with a complex and unclear mechanism of increased immune destruction or impaired production of platelets. While the management of ITP is evolving, there is still a
Externí odkaz:
https://doaj.org/article/054d63ab37a14969ae51686eef5b3e9e
Autor:
Ahmet Muzaffer Demir, Elif Gülsüm Ümit, Muhlis Cem Ar, Mesut Ayer, Meltem Aylı, Volkan Karakuş, Emin Kaya, Fahir Özkalemkaş, Nilgün Sayınalp, Mehmet Sönmez, Fahri Şahin, Selami Koçak Toprak, Tayfur Toptaş, İrfan Yavaşoğlu, Ümran Çalış
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 2, Pp 97-104 (2024)
Objective: Primary immune thrombocytopenia (pITP) is an acquired autoimmune disorder related to the increased destruction and/or impaired production of platelets. Its diagnosis and management are challenging and require expertise and the interpretati
Externí odkaz:
https://doaj.org/article/fb37fc3017d44f9e90832b4fba39d603
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:
Betül Kübra Tüzün, Ajda Güneş, Derya Demir, Nur Soyer, Mahmut Töbü, Filiz Vural, Serra Kamer, Selen Bayraktaroğlu, Fahri Şahin, Güray Saydam
Publikováno v:
HemaSphere, Vol 7, p e4131850 (2023)
Externí odkaz:
https://doaj.org/article/d3656e6faee64242bd296f637b137453
Publikováno v:
HemaSphere, Vol 7, p e912656b (2023)
Externí odkaz:
https://doaj.org/article/c6554e64877d48d6b61d1fbe0e27c00e
Autor:
Fergün Yılmaz, Nur Soyer, Güldane Cengiz Seval, Sinem Civriz Bozdağ, Pervin Topcuoğlu, Ali Ünal, Leylagül Kaynar, Gökhan Özgür, Gülsan Türköz Sucak, Hakan Göker, Mustafa Velet, Hakan Özdoğu, Mehmet Yılmaz, Emin Kaya, Ozan Salim, Burak Deveci, İhsan Karadoğan, Güray Saydam, Fahri Şahin, Filiz Vural
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 3, Pp 195-203 (2021)
Objective: Although inhibition of the complement system at different steps is a promising therapy modality in patients with paroxysmal nocturnal hemoglobinuria (PNH), allogeneic hematopoietic stem cell transplantation (HCT) is still the only curative
Externí odkaz:
https://doaj.org/article/5bce8903a2b2414e88326fb73088f77a
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
Autor:
Kaan Kavaklı, Bülent Antmen, Vahap Okan, Fahri Şahin, Selin Aytaç, Can Balkan, Ergül Berber, Zühre Kaya, Alphan Küpesiz, Bülent Zülfikar
Publikováno v:
Therapeutic Advances in Hematology, Vol 13 (2022)
Haemophilia is an X-linked lifelong congenital bleeding disorder that is caused by insufficient levels of factor VIII (FVIII; haemophilia A) or factor IX (FIX; haemophilia B) and characterized by spontaneous and trauma-related bleeding episodes. The
Externí odkaz:
https://doaj.org/article/64567dd6d59d469caa672f083dcdb98a
Autor:
Tahir Atik, Esra Işık, Hüseyin Onay, Bilçağ Akgün, Moharram Shamsali, Kaan Kavaklo, Melike Evim, Gülen Tüysüz, Namık Yaşar Özbek, Fahri Şahin, Zafer Salcıoğlu, Canan Albayrak, Yeşim Oymak, Ekrem Ünal, Fatma Burcu Belen, Ebru Yılmaz Keskin, Can Balkan, Birol Baytan, Alphan Küpesiz, Vildan Culha, Tuba Nur Tahtakesen, Adalet Meral Güneş, Ferda Özkınay
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Objective: Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey
Externí odkaz:
https://doaj.org/article/739b1796010f4465a28442c9b6243a1b