Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Yöntem, Yaman"'
Autor:
Yöntem Yaman, Sultan Aydin Köker, Fahri Yüce Ayhan, Ferah Genel, Can Acıpayam, Yeşim Oymak, Ebru Tuğrul Sarıbeyoğlu, Canan Raziye Vergin
Publikováno v:
Central European Journal of Immunology, Vol 44, Iss 2, Pp 206-209 (2019)
Leukocyte adhesion deficiency type II (LAD II) is a rare, autosomal, recessive inherited immunodeficiency disease that induces frequent and recurrent infections, persistent leukocytosis, severe mental and growth retardation, and impaired wound healin
Externí odkaz:
https://doaj.org/article/898ed3f8357a42869f007c3fb314c9e8
Autor:
Yöntem Yaman, Gökhan Baysoy, Emre Keleşoğlu, Kürşat Özdilli, Aslı Çakır, Dildar Bahar Genç, Murat Elli, Sema Anak
Publikováno v:
Contemporary Oncology, Vol 23, Iss 1, Pp 59-62 (2019)
In the pediatric population, hematopoietic stem cell transplantation (HSCT) is used to treat a wide variety of diseases, both malignant and nonmalignant. For many of these diseases, HSCT is a well-established treatment. Acute graft-versus-host diseas
Externí odkaz:
https://doaj.org/article/e4b345440111407fb98cedded1bff6be
Autor:
Brice Mouttet, Luciana Vinti, Philip Ancliff, Nicole Bodmer, Benoît Brethon, Gunnar Cario, Christiane Chen-Santel, Sarah Elitzur, Volkan Hazar, Joachim Kunz, Anja Möricke, Jerry Stein, Ajay Vora, Yöntem Yaman, Martin Schrappe, Sema Anak, André Baruche, Franco Locatelli, Arend von Stackelberg, Martin Stanulla, Jean-Pierre Bourquin
Publikováno v:
Haematologica, Vol 104, Iss 6 (2019)
Externí odkaz:
https://doaj.org/article/83295e8457244ae98d2e6f9132e8a551
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:
Ömer Faruk Beşer, Ayca Kiykim, Ali Islek, Serdar Nepesov, Gokhan Baysoy, Elif Karakoc-Aydiner, Sezin Aydemir, Yöntem Yaman, Haluk Cokugras, Bernice Lo, Yasemin Kendir Demirkol, Safa Baris, Satanay Hubrack, Fügen Çullu Çokuğraş, Ahmet Ozen
Publikováno v:
Journal of Clinical Immunology. 41:1406-1410
To the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, nutrient- and growth fact
Publikováno v:
Güncel Pediatri. 18:237-250
INTRODUCTION: Main purpose of this study is to evaluate the effects of some genetic modifiers; especially by correcting the imbalance between alpha/non alpha chains on clinical severity of Turkish beta Thalassemia patients. MATERIALS and METHODS: Eig
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
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.
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
Autor:
Sema Anak, Gokhan Baysoy, Dildar Bahar Genc, Emre Keleşoğlu, Yöntem Yaman, Murat Elli, Kürşat Özdilli, Asli Cakir
Publikováno v:
Contemporary Oncology
Contemporary Oncology, Vol 23, Iss 1, Pp 59-62 (2019)
Contemporary Oncology, Vol 23, Iss 1, Pp 59-62 (2019)
WOS: 000463814000008 PubMed ID: 31061639 In the pediatric population, hematopoietic stem cell transplantation (HSCT) is used to treat a wide variety of diseases, both malignant and nonmalignant. For many of these diseases, HSCT is a well-established