Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sema, Karakuş"'
Autor:
Emine Merve Savaş, Seda Yılmaz, Ayşe Asena Başer Dikyar, Zübeyde Nur Özkurt, Ramazan Öcal, Ferda Can, Sezgin Pepeler, Lale Aydın Kaynar, Sanem Gökçen, Abdulkerim Yıldız, Murat Albayrak, Sema Karakuş, Özcan Çeneli, Münci Yağcı
Publikováno v:
Turkish Journal of Hematology, Vol 40, Iss 4, Pp 236-241 (2023)
Objective: The discovery of imatinib was a milestone for chronic myeloid leukemia (CML). As the life expectancy of CML patients has approached that of the general population, research has shifted towards improving quality of life and economic conside
Externí odkaz:
https://doaj.org/article/dba536e5bd394b3b8141212902e2496b
Autor:
Eren Gündüz, Hakkı Onur Kırkızlar, Elif Gülsüm Ümit, Sedanur Karaman Gülsaran, Vildan Özkocaman, Fahir Özkalemkaş, Ömer Candar, Tugrul Elverdi, Selin Küçükyurt, Semra Paydaş, Özcan Çeneli, Sema Karakuş, Senem Maral, Ömer Ekinci, Yıldız İpek, Cem Kis, Zeynep Tuğba Güven, Aydan Akdeniz, Tiraje Celkan, Ayşe Hilal Eroğlu Küçükdiler, Gülsüm Akgün Çağlıyan, Ceyda Özçelik Şengöz, Ayşe Karataş, Tuba Bulduk, Alper Özcan, Fatma Burcu Belen Apak, Aylin Canbolat, İbrahim Kartal, Hale Ören, Ersin Töret, Gül Nihal Özdemir, Şule Mine Bakanay Öztürk
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 2, Pp 130-135 (2022)
Objective: Castleman disease (CD) is a rare disease also known as angiofollicular lymph node hyperplasia. The two main histological subtypes are the hyaline vascular and plasma cell variants. It is further classified as unicentric CD (UCD) or multice
Externí odkaz:
https://doaj.org/article/90602ce9f9bf437588736f9a063da92f
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 4, Pp 314-320 (2021)
Castleman disease is a rare lymphoproliferative disease also known as angiofollicular lymph node hyperplasia. It is classified as hyaline vascular and plasmacytic variants histologically but characteristics of both types can coexist. Most unicentric
Externí odkaz:
https://doaj.org/article/50e287e15131452398b26bd68534320b
Autor:
Yunus Kasım Terzi, Tuğçe Bulakbaşı Balcı, Can Boğa, Zafer Koç, Zerrin Yılmaz Çelik, Hakan Özdoğu, Sema Karakuş, Feride İffet Şahin
Publikováno v:
Turkish Journal of Hematology, Vol 33, Iss 4, Pp 320-325 (2016)
Objective: Hemochromatosis is an autosomal recessive disease that is one of the most important reasons for iron overload. Sickle cell disease is a hemoglobinopathy that occurs as a result of a homozygous mutation in the hemoglobin gene. Erythrocyte t
Externí odkaz:
https://doaj.org/article/4e00c686b20146568782a01414689f4d
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 2, Pp 121-127 (2014)
OBJECTIVE: Venous, arterial, and microcirculatory events are frequently encountered in the clinical course of essential thrombocytosis and polycythemia vera. We aimed to investigate the levels of soluble endothelial protein C receptor (sEPCR) in myel
Externí odkaz:
https://doaj.org/article/5d1ceb933cbb4aa3a2a816981ee1eeab
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 3, Pp 248-253 (2012)
OBJECTIVE: The accompanying thrombocytosis is referred to as the major factor associated with thromboembolism in iron deficiency anemia (IDA). Increased viscosity may increase the risk of thrombosis. We hypothesized that increased platelet count -wit
Externí odkaz:
https://doaj.org/article/5a43aafa2b39445ab17834da09fe25e4
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 3, Pp 293-296 (2012)
Externí odkaz:
https://doaj.org/article/903c5fb158074779a56f2b80749a9855
Autor:
Selami K. Toprak, Sema Karakuş
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 4, Pp 422-424 (2012)
Externí odkaz:
https://doaj.org/article/3ba68b421e204d47ab2857de490a820d
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 3, Pp 307-308 (2012)
Externí odkaz:
https://doaj.org/article/3cdade454a8446ca88f3e28410ae5b70
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 04, Pp 350-351 (2011)
Externí odkaz:
https://doaj.org/article/bb3aeba2a8224fc3960498a5556899de