Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Nihan, Bayram"'
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S27-S28 (2023)
Objective: Hemoglobinopaties are the most common genetic disorder worldwide. Patients with transfusion-dependent thalassemia major (TDT) are deficient in β-globulin chain production, resulting in ineffective erytropoiesis and hemolysis. Consequently
Externí odkaz:
https://doaj.org/article/c517074e0a794de2a0f60bf3bc760bd3
Autor:
Zeynep Akgiray, Enes Çandır, Aslı Çakır, Elif Çalış, Leyla Telhan, İrem İşlek, Mehmet Doğan, Yasemin Topçu, Alpay Cakmak, Nihan Bayram, Yöntem Yaman, Murat Elli, Sema Anak
We report a case of a 6-year-old girl, with the diagnosis of neurocutaneous melanomatosis (NCM). Presentation can be without significance and biopsy is required for the diagnosis. In literature our treatment protocol is striking and the quality of li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::470f5a05b6d917c34e8fa8a99d88195e
https://doi.org/10.22541/au.166359084.44583022/v1
https://doi.org/10.22541/au.166359084.44583022/v1
Autor:
Akif Ayaz, Zeynep Dogru, Feyza Bayramoglu, Kıvanç Kök, Nihan Bayram, Yöntem Yaman, Abdullah Hüseyin Köseoğlu, Türkan Yiğitbaşı, Aslı Güner Öztürk Demir, Elçin Yüksel, Burcu Dundar, Erdal Fırat Çaralan, Serdar Nepesov, Murat Elli
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f284a5aae624320d27942ee7c111767d
https://doi.org/10.2139/ssrn.4145478
https://doi.org/10.2139/ssrn.4145478
Autor:
Serdar, Nepesov, Yöntem, Yaman, Murat, Elli, Nihan, Bayram, Kürşat, Özdilli, Ayça, Kıykım, Deniz, Çakır, Betül, Kılıç, Kürşad, Aydın, Akif, Ayaz, Leyla, Telhan, Sema, Anak
Objectİive: In this study, we sought to describe the clinical, laboratory, and genetic characteristics of patients diagnosed with primary hemophagocytic lymphohistiocytosis. Thus, we aimed to evaluate the early diagnosis and appropriate treatment op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecb3bdf873a6ed8ac60397a4067bdb93
https://hdl.handle.net/20.500.12511/9637
https://hdl.handle.net/20.500.12511/9637
Objectives To describe the clinical characteristics of patients with chronic neutropenia. Methods Data of 36 patients with chronic neutropenia, who were followed up in the authors' clinic between May 2013 and May 2020, were analyzed retrospectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d792e5a07ef94e3b76abf0daedb17f48
https://hdl.handle.net/20.500.12511/9970
https://hdl.handle.net/20.500.12511/9970
Autor:
Sema Anak, Leyla Telhan, Nihan Bayram, Murat Elli, Suat H. Ayyildiz, Asli Cakir, Dilek Unal, Fatih Sebirli, Mehmet Dogan, Yöntem Yaman
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e900-e902
Background Hodgkin lymphoma (HL) is predominantly a nodal disease with extranodal presentation being uncommon. Presentation with neurological symptoms is not uncommon in adult patients with HL. Subdiaphragmatic involvements are less common especially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f6e3d52d3cc7bbbb273d2ee75615c76
https://doi.org/10.1097/mph.0000000000002186
https://doi.org/10.1097/mph.0000000000002186
Autor:
Sema Anak, Sude Sema Behar, Hülya Bilgen, Leyla Telhan, Kürşat Özdilli, Yöntem Yaman, Murat Elli, Serdar Nepesov, Nihan Bayram
Publikováno v:
Pediatric Transplantation. 25
Introduction (Ph-like) ALL is a subset of leukemia which has a gene expression profile similar to Ph+disease, but without the presence of BCR-ABL1 translocation. Case description We reported an exceptional case of a child with relapsed Ph-like ALL wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d64a0540fee2cd80cc8766fdf110002a
https://doi.org/10.1111/petr.14024
https://doi.org/10.1111/petr.14024
Autor:
Şifa Şahin, Kürşat Özdilli, Nihan Bayram, Sema Anak, Serdar Nepesov, Hülya Bilgen, Yöntem Yaman, Murat Elli
Publikováno v:
Pediatric Transplantation. 25
Delayed recovery of thrombocytopenia is a well-known complication after allogeneic HSCT. Eltrombopag (ELT), a thrombopoietin receptor agonist (TRAs), induces platelet maturation and release. Mostly conducted in adults, some of the previous studies ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9730a85432ed763d1b06c8dcebe9c605
https://doi.org/10.1111/petr.13962
https://doi.org/10.1111/petr.13962
Autor:
Yöntem Yaman, Murat Elli, Kürşat Özdilli, Leyla Telhan, Nihan Bayram, Volkan Hazar, Ebru Tuğrul Sarıbeyoğlu, Şifa Şahin, Seniye Anak
Giriş: Standart tedavi alan Hodgkin Lymphoma (HL) hastalarının yaklaşık %20’sinde hastalık dirençli seyredebilir veya tekrar edebilir. Tekrar eden/ dirençli HL’da standart tedavi yüksek doz kemoterapi ve takip eden otolog kök hücre nak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cf1aa494bce653829a4980777582eb4
https://hdl.handle.net/20.500.12511/10674
https://hdl.handle.net/20.500.12511/10674