Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Dilek Kaçar"'
Autor:
Burçin Kurtipek, Ayça Koca Yozgat, Saliha Kanık Yüksek, Dilek Kaçar, Turan Bayhan, Dilek Gürlek Gökçebay, Aslınur Özkaya Parlak, Neşe Yaralı
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)
Background: Port catheters facilitate the administration of chemotherapy, antibiotics, blood products, fluid and parenteral nutritional support to pediatric patients with hematological malignancies. However, as its use has become widespread, local, a
Externí odkaz:
https://doaj.org/article/846b24b1e3a44a088000b48979722976
Autor:
Ayça Koca Yozgat, Derya Özyörük, Suna Emir, Ahmet Demir, Arzu Yazal Erdem, Can Barış Aker, Zeliha Güzelküçük, İnci Yaman Bajin, Dilek Kaçar, Neşe Yaralı, Namık Yaşar Özbek
Publikováno v:
The Journal of Pediatric Academy, Vol 4, Iss 2, Pp 62-66 (2023)
Cancer care is progressively became as a significant worldwide challenge. Wars can cause destructions and delays in cancer diagnosis and treatment of displaced people. Cancer cure rates need to be improved in indefensible populations such as refugees
Externí odkaz:
https://doaj.org/article/e7cf13b172f04975a107ea08a4e87c32
Autor:
Ayça Koca Yozgat, Fatma Burçin Kurtipek, Zeliha Güzelküçük, Dilek Kaçar, Turan Bayhan, Namık Yaşar Özbek, Neşe Yaralı
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S25- (2023)
Objective: Congenital neutropenia (CN) is a rare inherited hematological disease and its phenotypic, histologic and molecular aspects are heterogeneous. Congenital neutropenia can manifest as isolated neutropenia or neutropenia with extra-hematopoiet
Externí odkaz:
https://doaj.org/article/4fd730349c09423192f82efdd58e14fa
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S25- (2023)
Objective: Polyoma BK virus (BKV) infection/reactivation is an important underlying condition that provokes hemorrhagic cystitis (HC) in hematopoietic stem cell transplantation (HSCT) recipients. However, BKV associated infections can rarely occur in
Externí odkaz:
https://doaj.org/article/5f6d7764b94f4fb083f9693e9b85554e
Autor:
Özlem Arman Bilir, İbrahim İlker Çetin, Dilek Kaçar, Can Barış Aker, Namık Yaşar Özbek, Neşe Yaralı
Publikováno v:
Anatolian Journal of Cardiology, Vol 26, Iss 1, Pp 57-62 (2022)
Objective: Anthracyclines are widely used in the treatment of acute lymphoblastic leukemia (ALL). However, cardiotoxicity is the most critical side effect that requires dose limitation. It is thought to occur at first exposure, but the clinical prese
Externí odkaz:
https://doaj.org/article/6ecfc1e45a354d63bdd8ba7eb9d06c4c
Autor:
Yunus Murat Akcabelen, Dilek Kaçar, Ayça Koca Yozgat, Özlem Arman Bilir, Dilek Gürlek Gökçebay, Turan Bayhan, İkbal Ok Bozkaya, Namık Yaşar Özbek, Neşe Yaralı
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S25- (2021)
Objective: In the 5-year follow-up of patients diagnosed with Juvenile Myelomonocytic Leukemia (JMML) in a single center; reveal treatment and survival analyzes Methodology: In this study, clinical and laboratory data of 12 JMML patients followed in
Externí odkaz:
https://doaj.org/article/a72aeab0c8db4fee96fe6f0fc022886b
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S25-S26 (2021)
Objective: Intrachromosomal amplification of chromosome 21 (iAMP21) is defined as the presence of three or more RUNX1 signals on a single chromosome, or a total of five or more RUNX1 signals per cell. It occurs in 2% of pediatric B-cell acute lymphob
Externí odkaz:
https://doaj.org/article/c9c61f0e417f4c0d8ab14cdbfe8bc9c8
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S28-S29 (2021)
Case report: tRNA nucleotidyltransferase 1(TRNT1) gene encodes a polymerase involved in the maturation of cytosolic and mitochondrial transfer RNAs. Autosomal recessive loss of function mutations of TRNT1 leads sideroblastic anemia, immunodeficiency,
Externí odkaz:
https://doaj.org/article/eff16e9435ff46f8a12425779f3935a0
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S59- (2021)
Case report: We present three children with precursor B acute lymphoblastic leukemia (ALL). The first one had malignancy associated hypercalcemia at diagnosis. The second one experienced hyperamonemia during induction. Both of them had been treated s
Externí odkaz:
https://doaj.org/article/f3b136323ea847eeae39d3625e82d192
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S58- (2021)
Objective: Compared with other cytogenetic acute myeloid leukemia (AML) groups, patients with core-binding factor AML (CBF-AML) are considered as a favorable AML risk group based on their high remission rate and survival probabilities. However, up to
Externí odkaz:
https://doaj.org/article/c730cbd83d9b47a2b003989b8214ddab