Cigdem Binay
Eskişehir Osmangazi University
27 Papers
82 Citations
Cigdem Binay is an academic researcher from Eskişehir Osmangazi University. The author has contributed to research in topics: Medicine & Turner syndrome. The author has an hindex of 7, co-authored 25 publications.
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Papers
Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
Ediz Yeşilkaya,Abdullah Bereket,Feyza Darendeliler,Firdevs Bas,Sukran Poyrazoglu,Banu Kucukemre Aydin,Şükran Darcan,Bumin Dündar,Muammer Buyukinan,Cengiz Kara,Erkan Sari,Erdal Adal,Ayşehan Akıncı,Mehmet Emre Atabek,Fatma Demirel,Nurullah Çelik,Behzat Özkan,Bayram Özhan,Zerrin Orbak,Betül Ersoy,Murat Doğan,Ali Ataş,Serap Turan,Damla Gökşen,Ömer Tarım,Bilgin Yüksel,Oya Ercan,Şükrü Hatun,Enver Simsek,Ayşenur Ökten,Ayhan Abaci,Hakan Doneray,Mehmet Nuri Ozbek,Mehmet Keskin,Hasan Önal,Nesibe Akyürek,Kezban Bulan,Derya Tepe,Hamdi Cihan Emeksiz,Korcan Demir,Deniz Özalp Kızılay,Ali Kemal Topaloglu,Erdal Eren,Samim Özen,Saygin Abali,Leyla Akin,Beray Selver Eklioğlu,Sultan Kaba,Ahmet Anık,Serpil Bas,Tolga Ünüvar,Halil Saglam,Semih Bolu,Tolga Özgen,Durmuş Doğan,Esra Deniz Çakır,Yaşar Şen,Nesibe Andiran,Filiz Mine Çizmecioğlu,Olcay Evliyaoğlu,Gülay Karagüzel,Ozgur Pirgon,Gönül Çatlı,Hatice Dilek Can,Fatih Gurbuz,Cigdem Binay,Veysel Nijat Baş,Kursat Fidanci,Adem Polat,Davut Gül,Cengizhan Açıkel,Huseyin Demirbilek,Peyami Cinaz,Carolyn Bondy +73 more
TL;DR: The karyotype distribution, congenital anomaly and comorbidity profile closely parallel that from other countries and support the need for close medical surveillance of these complex patients throughout their lifespan.
The correlation between GnRH stimulation testing and obstetric ultrasonographic parameters in precocious puberty.
TL;DR: It was found that LH levels, peak LH/FSH ratio, fundal/cervical ratio, uterus length, and ovarian volume were reliable predictors of central precocious puberty (CPP) and obstetric ultrasound parameters represent reliable predictor for the diagnosis of CPP.
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Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey
Sukran Poyrazoglu,Rüveyde Bundak,Zehra Yavas Abali,Hasan Önal,Sevil Sarikaya,Abdurrahman Akgun,Serpil Bas,Saygin Abali,Abdullah Bereket,Erdal Eren,Ömer Tarım,Ayla Güven,Metin Yildiz,Derya Karaman Aksakal,Aysegul Yuksel,Gulcan Seymen Karabulut,Şükrü Hatun,Şükrü Hatun,Tolga Özgen,Yaşar Cesur,Mehmet Azizoğlu,Emine Dilek,Filiz Tutunculer,Esra Deniz Papatya Cakir,Bahar Ozcabi,Olcay Evliyaoğlu,Songül Karadeniz,Fatma Dursun,Semih Bolu,Ilknur Arslanoglu,Gül Yeşiltepe Mutlu,Heves Kırmızıbekmez,Pinar Isguven,Ala Üstyol,Erdal Adal,Ahmet Uçar,Nurcan Cebeci,Didem Bezen,Cigdem Binay,Serap Semiz,Hüseyin Anıl Korkmaz,Nihal Memioglu,Elif Sagsak,Havva Nur Peltek,Melek Yildiz,Teoman Akcay,Serap Turan,Tulay Guran,Zeynep Atay,Nese Akcan,Filiz Mine Çizmecioğlu,Oya Ercan,Aydilek Dağdeviren,Firdevs Bas,Halim Issever,Feyza Darendeliler +55 more
TL;DR: The northwest region of Turkey experienced an intermediate incidence of T1DM over the period of the study and a significant increase in the proportion of cases diagnosed was observed in the autumn-winter seasons.
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Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study.
Şükrü Hatun,Huseyin Demirbilek,Şükran Darcan,Aysegul Yuksel,Cigdem Binay,Damla Gökşen Şimşek,Cengiz Kara,Ergun Cetinkaya,Tolga Ünüvar,Ahmet Uçaktürk,Filiz Tutunculer,Yaşar Cesur,Rüveyde Bundak,Halil Saglam,Enver Simsek,Abdullah Bereket +15 more
TL;DR: Promoting use of carbohydrate count and insulin correction doses may improve the glycemic control of pediatric T1DM in Turkey.
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Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency.
Enver Simsek,Luciana Ribeiro Montenegro,Cigdem Binay,Meliha Demiral,Mustafa Fuat Acıkalin,Ana Claudia Latronico +5 more
TL;DR: An adolescent male with isolated FSH deficiency due to a novel FSHβ gene mutation associated with a prepubertal testes size and normal virilisation is described and recombinant human FSH (rhFSH) replacement is demonstrated.
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