Zobrazeno 1 - 10
of 81
pro vyhledávání: '"KARAKAYA, CENGİZ"'
Publikováno v:
In Journal of Pediatric Urology August 2024
Autor:
Erdem, Mehmet, Erdem, Ahmet, Mutlu, Mehmet Firat, Ozisik, Seckin, Yildiz, Sule, Guler, Ismail, Karakaya, Cengiz
Publikováno v:
In European Journal of Obstetrics and Gynecology February 2016 197:120-124
Autor:
TURAL, Rabia1, KARAKAYA, Cengiz1 karakayac@gazi.edu.tr, ERDEM, Mehmet2,3, AYKOL, Zeynep3, KARABACAK, Recep Onur2, KAVUTÇU, Mustafa1
Publikováno v:
Turkish Journal of Medical Sciences. 2021, Vol. 51 Issue 4, p1969-1975. 7p.
Autor:
Karakaya, Cengiz, Guzeloglu-Kayisli, Ozlem, Uyar, Asli, Kallen, Amanda N., Babayev, Elnur, Bozkurt, Nuray, Unsal, Evrim, Karabacak, Onur, Seli, Emre
Publikováno v:
In Fertility and Sterility June 2015 103(6):1469-1476
Autor:
Oktem, Mesut, Ozcan, Pinar, Erdem, Ozlem, Karakaya, Cengiz, Cenksoy, Cahit, Guner, Haldun, Karabacak, Onur, Dursun, Polat
Publikováno v:
In European Journal of Obstetrics & Gynecology and Reproductive Biology September 2014 180:120-125
Autor:
CEVHER AKDULUM, MÜNİRE FUNDA, ŞAHİN, ESİN, DEMİRDAĞ, ERHAN, ERDEM, AHMET, GÜLER, İSMAİL, ERDEM, MEHMET, KARAKAYA, CENGİZ
Publikováno v:
Gazi Medical Journal. 33
Objective: To evaluate whether hCG day serum LH levels have an impact on IVF outcomes in patients undergoing GnRH antagonist protocols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a69030b38bb7aac5b387b02dd6f30dcb
https://doi.org/10.12996/gmj.2022.38
https://doi.org/10.12996/gmj.2022.38
Autor:
Karakaya, Cengiz, Çil, Aylin Pelin, Bilguvar, Kaya, Çakir, Tunahan, Karalok, Mete Hakan, Karabacak, Recep Onur, Caglayan, Ahmet Okay
Publikováno v:
J Obstet Gynaecol Res
AIM: To identify pathogenic rare coding Mendelian/high-effect size variant(s) by whole-exome sequencing in familial PCOS patients to elucidate PCOS related pathways. METHODS: Twenty women and their affected available relatives diagnosed with polycyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce162984d370b285583f956a10c32aec
https://europepmc.org/articles/PMC9050819/
https://europepmc.org/articles/PMC9050819/
Autor:
ÇAKIR, TUNAHAN, KARAKAYA, CENGİZ, ÇAĞLAYAN, AHMET OKAY, KARABACAK, RECEP ONUR, Karalok, Mete Hakan, Cil, Aylin Pelin, Bilguvar, Kaya
Aim To identify pathogenic rare coding Mendelian/high-effect size variant(s) by whole-exome sequencing in familial polycystic ovary syndrome (PCOS) patients to elucidate PCOS-related pathways. Methods Twenty women and their affected available relativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9d39fa27696de57d8a6c8bb1fb06da67
https://avesis.deu.edu.tr/publication/details/e374fa2e-dfa6-4e62-a3dd-bf6f1cca1bcd/oai
https://avesis.deu.edu.tr/publication/details/e374fa2e-dfa6-4e62-a3dd-bf6f1cca1bcd/oai
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Akademický článek
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