Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mehmet Ozgur Akkurt"'
Autor:
Yakup Yalcin, Serenat Eris Yalcin, Selda Uysal, Burak Tatar, And Yavuz, Mehmet Ozgur Akkurt, Seyran Yigit
Publikováno v:
Medicine Science, Vol 8, Iss 4, Pp 774-781 (2019)
The aim of our study is to evaluate whether CD 44 isoform expression is a prognostic factor in vulvar carcinom and to correlate the expression with clinicopathological parameters. Methods: The study included 26 patients diagnosed with invasive squamo
Externí odkaz:
https://doaj.org/article/7ca39879a3c64fbda3627774b322e431
Autor:
Bora Coskun, Berna Dilbaz, Burak Karadag, Bugra Coskun, Yusuf Aytac Tohma, Riza Dur, Mehmet Ozgur Akkurt
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 5, Pp 713-717 (2018)
Objective: To determine the role of anti-Mullerian hormone (AMH) levels in predicting the response to clomiphene citrate (CC) therapy for ovulation induction in women with unexplained infertility. Materials and methods: For this retrospective study,
Externí odkaz:
https://doaj.org/article/8a4d2c6f17c44514baa5bf8cc13c9df5
Autor:
Cetin Aydin, Serenat Eris Yalcin, Yakup Yalcin, Dilek Uysal, Mehmet Ozgur Akkurt, And Yavuz, Halime Sen Selim, Esra Nur Tola
Publikováno v:
Medicine Science, Vol 5, Iss 4, Pp 941-4 (2016)
The aim of our study is to provide a population-based risk factor profile for placenta previa and thereby enable early diagnosis plus the necessary management for this risky group. Methods This research was a retrospective case control study includin
Externí odkaz:
https://doaj.org/article/33317519b5fc41ee8d8f1635cd60e500
Publikováno v:
Cukurova Medical Journal, Vol 42, Iss 2, Pp 376-379 (2017)
Konjenital diafragmatik herni eşlik edebilecek diğer organ anomalileri riskinin arttığı, sık görülen bir toraks anomalisidir. Kesin etyolojisi bilinmemekle beraber, olası nedeni primordiyal diafragmanın amuskuler parçasındaki kusurdur. Ko
Externí odkaz:
https://doaj.org/article/4864891c0f544282a2d58c4ad679555c
Publikováno v:
Cukurova Medical Journal, Vol 42, Iss 1, Pp 189-191 (2017)
13. kromozomun uzun kolundaki parsiyel delesyon mental retardasyon, gelişme geriliği ve çeşitli konjenital malformasyonlarla karakterize nadir görülen kromozomal bir bozukluktur. Etkilenenlerin fenotipleri delesyonun lokasyon ve boyutuna göre
Externí odkaz:
https://doaj.org/article/c7ce215ddf5d4e0e93e0f4c43f1be5c7
Publikováno v:
Balkan Medical Journal, Vol 32, Iss 4, Pp 426-428 (2015)
Background: Utero-cutaneous fistula (UCF) is an extremely rare entity and only a few case reports have been published. Most UCFs develop secondary to postpartum or postoperative complications. Case Report: A 42 year-old woman began to complain fro
Externí odkaz:
https://doaj.org/article/338dd7b572354a8496767bf596e31b81