Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Aynur Uğur Bilgin"'
Publikováno v:
Genel Tıp Dergisi, Vol 27, Iss 1, Pp 33-35 (2017)
Kronik lenfositik lösemi ve Mantle hücreli lenfoma da yeni bir tedavi seçeneği olan ibrutinib, yüksek etkinliği ile günümüzde sık kullanılmaya başlanmıştır. Hedefe yönelik monoklonal antikorların yan etkileri sitotoksik tedavilere g
Externí odkaz:
https://doaj.org/article/e875cb3bf05943bb82a0f4e2b4787d24
Autor:
Aynur Uğur Bilgin
Publikováno v:
Genel Tıp Dergisi, Vol 24, Iss 1, Pp 38-44 (2014)
Kanser ilişkili halsizlik ve fiziksel performans düşüklüğü kemoterapi sırasında ve sonrasında en sık rastlanılan problemlerdir. Anemi, beslenme bozuklukları, hormonal değişiklikler, psikososyal faktörler ve azalmış aktivite başlıc
Externí odkaz:
https://doaj.org/article/354c31f145914b9e9cb7827909f63a6a
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 2, Pp 194-196 (2014)
Externí odkaz:
https://doaj.org/article/71561e382ff746d0ba79d2cee84a198d
Publikováno v:
Balkan Medical Journal, Vol 33, Iss 5, Pp 581-582 (2016)
Externí odkaz:
https://doaj.org/article/7b3bdb0851e94e85ae1a5597104213e6
Autor:
İsmail Baloğlu, Aynur Uğur Bilgin
Publikováno v:
Selcuk Tip Dergisi. 2:94-98
\n Introduction: Multipl myeloma is a disease of unknown pathogenesis. Although there was a different\n\n hypotheses on the subject, recently mutations in the pathway of apoptosis come to the fore. PUMA may play a role in apoptosis, bound or\n\n unbo
Autor:
Aynur Uğur Bilgin1 aynurugurbilgin@yahoo.com
Publikováno v:
Journal of General Medicine / Genel Tıp Dergisi. 2014, Vol. 24 Issue 1, p38-44. 7p.
Publikováno v:
Transfusion and Apheresis Science. 50:433-437
Thrombotic thrombocytopenic purpura (TTP) is an uncommon, severe, potentially life-threatening disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, altered mental status, fever, and renal abnormalities. It can be seen at any
Publikováno v:
Transfusion and Apheresis Science. 52:214-216
Immune thrombocytopenia (ITP) is an acquired immune-mediated disease characterized by persistant thrombocytopenia. Onset of the disease and the clinical course is highly variable, but the disease typically has a benign course. Patients rarely develop
Autor:
Mutlu Arat, Mehmet Bektas, Esra Erden, Ramazan Idilman, Aynur Uğur Bilgin, Onder Arslan, Sule Mine Bakanay
Publikováno v:
The Turkish Journal of Gastroenterology. 24:359-362
In this paper, we report the case of a 19-year-old male patient who presented with lymphoblastic phase of chronic myeloid leukemi- a and received an allogeneic bone marrow transplant from his cousin. The patient experienced severe, steroid-refractory
Autor:
Ayşen, Timurağaoğlu, Aynur, Uğur Bilgin, Murat, Tuncer, İlhan, Gölbaşı, Dilek, Çolak, Seray, Dizlek, Gülten, Karpuzoğlu
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 22(4)
Posttransplant lymphoproliferative disorder (PTLD) is a serious complication of organ transplantation, with a reported incidence between 0.8% to 32%. Herein we retrospectively analyzed the patients who diagnosed as PTLD in Akdeniz University. Within