Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Sevilhan Artan"'
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:
Nazlı Durmaz Çelik, Ebru Erzurumluoğlu, Serkan Özben, Uğur Toprak, Göknur Yorulmaz, Sevilhan Artan, Serhat Özkan
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-10 (2023)
Abstract Background Gordon Holmes syndrome (GHS) is a rare autosomal recessive disorder characterized by hypogonadotropic hypogonadism, cognitive decline, and cerebellar ataxia. Mutations in the Ring Finger Protein 216 (RNF216) gene have been known t
Externí odkaz:
https://doaj.org/article/3971ccdb6c7948cdac240c1072e859e3
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:
Taner Ulus, Muhammet Dural, Pelin Meşe, Furkan Yetmiş, Kadir Uğur Mert, Bülent Görenek, Oğuz Çilingir, Ebru Erzurumluoglu Gökalp, Serap Arslan, Sevilhan Artan, Özlem Aykaç, Ertuğrul Çolak, Hikmet Yorgun, Uğur Canpolat, Kudret Aytemir
Publikováno v:
Anatolian Journal of Cardiology, Vol 25, Iss 2, Pp 129-138 (2021)
Externí odkaz:
https://doaj.org/article/d032af3eeb744039a65db6728dd5a1fb
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:
Orcun Unal, Mustafa Ozer Ulukan, Vedat Bakuy, Behiye Kaytaz, Sevilhan Artan, Erinc Aral, Didem Melis Oztas, Metin Onur Beyaz, Murat Ugurlucan, Behcet Sevin
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 35, Iss 5, Pp 626-633 (2020)
Abstract Objective: To detect and to compare the apoptotic effects of intraoperatively topically applied diltiazem, papaverine, and nitroprusside. Methods: Internal thoracic artery segments of ten patients were obtained during coronary bypass graftin
Externí odkaz:
https://doaj.org/article/a4138a009e7347a59cdc8a0cc81ecec7
Publikováno v:
Asian Pacific Journal of Reproduction, Vol 4, Iss 1, Pp 41-43 (2015)
Through cytogenetic analysis, heteromorphisms were detected in chromosomes 1,9,16 and Y and defined as non-phenotypic variations. The polymorphism in the centromeric heterochromatin region of chromosome 6 is a rare variant, and only five cases have b
Externí odkaz:
https://doaj.org/article/52d6fb22ced84f9fa8526b08f8e6a289
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:
Demet Özbabalık Adapınar, Suzan Saylısoy, Çınar Yenilmez, Hüseyin Aslan, Bengü Ertan, Sevilhan Artan, Gülcan Güleç, Çiğdem Susuz, Baki Adapınar
Publikováno v:
Dementia and Geriatric Cognitive Disorders Extra, Vol 1, Iss 1, Pp 429-432 (2011)
Variant Creutzfeldt-Jakob disease (vCJD) was first reported in the UK in 1996. Here, we report the first Turkish case of vCJD. A 47-year-old man, who has never lived outside of Turkey and had had no transfusion, was admitted to the University Hospita
Externí odkaz:
https://doaj.org/article/4058f0b167f845abb7a6787905e3fb3a
Publikováno v:
International Journal of Endocrinology, Vol 2014 (2014)
Background. Nonclassic congenital adrenal hyperplasia (NCAH), caused by mutations in the gene encoding 21-hydroxylase, is a common autosomal recessive disorder. In the present work, our aim was to determine the prevalence of NCAH presenting as premat
Externí odkaz:
https://doaj.org/article/8707a38d075d4b4c8a08fb748582a7a1