Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Beyhan Durak Aras"'
Autor:
Hasan Baş, Selçuk Dişibeyaz, Erkin Öztaş, Yusuf Aydemir, Tuncer Temel, Oğuz Çilingir, Beyhan Durak Aras, Sevilhan Artan
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 34, Iss 12, Pp 1240-1248 (2023)
Externí odkaz:
https://doaj.org/article/35d65c57ac6e4093be9183b170d36f66
Autor:
Sevgi Işık, Gülçin Günden, Hava Üsküdar Teke, Olga Meltem Akay, Nur Oğuz Davutoğlu, Vahap Aslan, Mustafa Karagülle, Hülya Özen, Oğuz Çilingir, Sevilhan Artan, Beyhan Durak Aras
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 4, Pp 237-244 (2022)
Objective: Objective: Chronic myeloid leukemia (CML) is a clonal hematologic disorder characterized by t(9;22) translocation, in which cytogenetic aberrations can occur in Ph(+) and (-) clones. These aberrations develop due to clonal evolution as wel
Externí odkaz:
https://doaj.org/article/a95fde8945ec4d30beebeb0b5d0db1a9
Autor:
Beyhan Durak Aras, Sevgi Isik, Hava Uskudar Teke, Abdulvahap Aslan, Filiz Yavasoglu, Zafer Gulbas, Fatih Demirkan, Hulya Ozen, Oguz Cilingir, Nur Sena Inci, Gulcin Gunden, Tuba Bulduk, Ebru Erzurumluoglu Gokalp, Sinem Kocagil, Sevilhan Artan, Olga Meltem Akay
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Background Deletion of 13q14 [del(13q)] is the most common cytogenetic change (50%) in chronic lymphoblastic leukemia (CLL), and it is a good prognostic factor if it is detected as a sole aberration by FISH. However, it is observed the clini
Externí odkaz:
https://doaj.org/article/ce7069f8615f4634a0687320dd93d0ec
Autor:
Hava Üsküdar Teke, Nur Oğuz Davutoğlu, Eren Gündüz, Neslihan Andıç, Cengiz Bal, Beyhan Durak Aras
Publikováno v:
İstanbul Medical Journal, Vol 18, Iss 4, Pp 200-204 (2017)
Introduction: Acute myeloid leukemia (AML) is an aggressive clonal myeloid neoplasm that causes the accumulation of myeloblasts in blood and bone marrow. This study aimed to determine immunophenotypic characteristics and their prognostic value in pat
Externí odkaz:
https://doaj.org/article/a4b48c38a5654549becf52b6a22660f7
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 1, Iss 4, Pp 80-82 (2016)
Myeloid sarcoma (MS) is the tumor of immature myeloid cells involving extramedullary sites. Liver involvement of MS is rare in infant. Three months old female infant presented with hepatosplenomegaly and bicytopenia. Repeated bone marrow aspiration d
Externí odkaz:
https://doaj.org/article/16d3536e956a4cd59b25f668de7693ea
Autor:
Beyhan Durak Aras, Olga Meltem Akay, Gülçin Sungar, Güney Bademci, Vahap Aslan, Jülide Caferler, Muhsin Özdemir, Oğuz Çilingir, Sevilhan Artan, Zafer Gülbaş
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 2, Pp 135-142 (2012)
OBJECTIVE: Multiple myeloma (MM) is characterized by the accumulation and proliferation of malignant plasma cells, secreting monoclonal immunoglobulins and genetic abnormalities in MM have implications for disease progression and survival. In the pre
Externí odkaz:
https://doaj.org/article/3ed158a9a8f643929c7d05ec7f5a8a99
Autor:
Neslihan Andıç, Beyhan Durak Aras, Eda Tatlipinar, Sevgi Ozpolat, Hava Uskudar Teke, Eren Gunduz, Meltem Olga Akay
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 1 (2014)
Externí odkaz:
https://doaj.org/article/f01fcac9fda848589e103afd193c406a
Autor:
Neslihan Andıç, Beyhan Durak Aras, Deniz Goren Sahin, Mustafa Karagulle, Hava Uskudar Teke, Eren Gunduz, Meltem Olga Akay
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 1 (2014)
Hydoxyuera has been widely used in treatment of patients with essential thrombocythemia (ET). There is a lack of definitive information about it's leukomogenic potential. Choromosomal abnormalities are found to be rare at diagnosis in ET patients. He
Externí odkaz:
https://doaj.org/article/06c7de3d609942449c254b86f3427d19
Autor:
Elif Uzay, Hasan Bas, Oguz Cilingir, Neslihan Tekin, Beyhan Durak Aras, Ebru Erzurumluoglu Gokalp, Sevilhan Artan, Suzan Saylisoy
Publikováno v:
American Journal of Medical Genetics Part A. 182:740-745
S-adenosylhomocysteine hydrolase deficiency is an autosomal recessive neurometabolic disorder affecting the muscles, liver, and nervous system. The disease occurs by pathogenic variants of AHCY gene encoding S-adenosylhomocysteine hydrolase (AHCY) en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c42d4dd41e45218b83357e4dd22ca8a
https://doi.org/10.1002/ajmg.a.61489
https://doi.org/10.1002/ajmg.a.61489
Publikováno v:
Acta Oncologica Turcica. 53:245-249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::549350fa90fe54511a6d754567964945
https://doi.org/10.5505/aot.2020.40316
https://doi.org/10.5505/aot.2020.40316