Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Yaşar, Bekir"'
Autor:
İleri, Alper, Yıldırım Karaca, Suna, İleri, Hande, Karaca, İbrahim, Gölbaşı, Hakan, Özer, Mehmet, Budak, Adnan, Kutbay, Yasar Bekir, Koç, Altuğ, Özeren, Mehmet
Publikováno v:
In Journal of Gynecology Obstetrics and Human Reproduction October 2023 52(8)
Autor:
Aksu Uzunhan, Tuğçe, Ertürk, Biray, Aydın, Kürşad, Ayaz, Akif, Altunoğlu, Umut, Yarar, Murat Hakkı, Gezdirici, Alper, İçağasıoğlu, Dilara Füsun, Gökpınar İli, Ezgi, Uyanık, Bülent, Eser, Metin, Kutbay, Yaşar Bekir, Topçu, Yasemin, Kılıç, Betül, Bektaş, Gonca, Arduç Akçay, Ayfer, Ekici, Barış, Chousein, Amet, Avcı, Şahin, Yüksel, Atıl, Kayserili, Hülya
Publikováno v:
In Clinical Neurology and Neurosurgery January 2023 224
Autor:
Özge Köprülü, Sezer Acar, Kadri Murat Erdoğan, Özlem Nalbantoğlu, Tarık Kırkgöz, Gülçin Arslan, Beyhan Özkaya, Yaşar Bekir Kutbay, Behzat Özkan
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 4, Pp 401-408 (2022)
The 45,X/47,XYY mosaicism is an extremely rare genetic disorder with highly phenotypic manifestations such as ovotesticular disorders of sexual development, mixed gonadal dysgenesis and Turner syndrome. Herein, we report two cases with very distincti
Externí odkaz:
https://doaj.org/article/ac925d37e44443fb9c358adf8d8c2b2a
Autor:
Berk Özyılmaz, Gül Caner Mercan, Özgür Kırbıyık, Taha Reşid Özdemir, Samira Özkara, Özge Özer Kaya, Yaşar Bekir Kutbay, Kadri Murat Erdoğan, Merve Saka Güvenç, Altuğ Koç
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 57, Iss 3, Pp 140-148 (2019)
Objective:The aim of this study is to investigate the efficiency of a first-line molecular genetic evaluation approach, in children with deafness.Methods:Patients who were found to have sensorineural hearing loss by age-appropriate audiological tests
Externí odkaz:
https://doaj.org/article/66a97428e8c94324ac5de34e16d365bb
Autor:
Tuba Demirci Yıldırım, Utku Erdem Soyaltın, Altuğ Koç, Serkan Yıldız, Mehmet Tanrısev, Yaşar Bekir Kutbay, Ferhat Ekinci, Süleyman Yıldırım, Harun Akar, Cengiz Ceylan
Publikováno v:
The Journal of Tepecik Education and Research Hospital. 33:45-49
Autor:
Demirci Yıldırım, Tuba, CEYLAN, Cengiz, AKAR, Harun, Yildirim, Suleyman, EKİNCİ, Ferhat, KUTBAY, Yaşar Bekir, Tanrisev, Mehmet, YILDIZ, Serkan, SOYALTIN, Utku Erdem, KOÇ, Altuğ
Objective: Glomerulonephritis (GN) a heterogeneous group disease and the pathophysiology of GN is not understood yet. The aim of the study, the investigation frequency of Janus kinase (JAK)2 gene mutation in GN. Methods: The study was conducted in Un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2605::4a3dfdf4304f2a85d7aee20b3bee9a73
https://avesis.deu.edu.tr/publication/details/7ce5a59b-f3af-437a-9919-d9325df792e9/oai
https://avesis.deu.edu.tr/publication/details/7ce5a59b-f3af-437a-9919-d9325df792e9/oai
Akademický článek
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Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 197-199 (2017)
Externí odkaz:
https://doaj.org/article/c6d3d28405194af78e7e28e0b1ce6541
Autor:
Yıldırım, Tuba Demirci, Soyaltın, Utku Erdem, Koç, Altuğ, Yıldız, Serkan, Tanrısev, Mehmet, Kutbay, Yaşar Bekir, Ekinci, Ferhat, Yıldırım, Süleyman, Akar, Harun, Ceylan, Cengiz
Publikováno v:
Journal of Tepecik Education & Research Hospital / İzmir Tepecik Eğitim ve Araştırma Hastanesi Dergisi; 2023, Vol. 33 Issue 1, p45-49, 5p
Autor:
Alper İLERİ, Suna YILDIRIM KARACA, Hande İLERİ, Hakan GÖLBAŞI, Alkım Gülşah ŞAHİNGÖZ YILDIRIM, Yaşar Bekir KUTBAY, Altuğ KOÇ, Mehmet ÖZEREN
Objective: Non-invasive prenatal testing (NIPT) and fetal fraction (FF) are shown to be affected by various factors like maternal characteristics or medications. Recently medications are now undergoing evaluation as influencing factors. Still no data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e88b8010a3634769ade2d0ce3892bccc
https://hdl.handle.net/11454/78947
https://hdl.handle.net/11454/78947