Davut Gül
Military Medical Academy
47 Papers
305 Citations
Davut Gül is an academic researcher from Military Medical Academy. The author has contributed to research in topics: Familial Mediterranean fever & Turner syndrome. The author has an hindex of 13, co-authored 47 publications.
Chat about Author
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.
Study of Autoimmunity in Klinefelter's Syndrome and Idiopathic Hypogonadotropic Hypogonadism
Cagatay Oktenli,Zeki Yesilova,Ismail H. Kocar,Ugur Musabak,Metin Ozata,Ali Inal,Davut Gül,Yavuz S. Sanisoglu +7 more
TL;DR: The findings suggest that both humoral and cellular immunity is enhanced in male hypogonadism and it is possible that testosterone deficiency and increased levels of estradiol are primary responsible factors for this enhanced autoantibody production in Klinefelter's syndrome patients.
36
A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patients
TL;DR: The study showed that R761H mutations were higher than it has been reported in literature until now and were mainly associated with M694V and should be included in the mutation scanning analysis researches or considered if the patient has M694Vs mutation especially in Turkish FMF patients.
34
Evaluation of the relationship between C677T variants of methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in children receiving antiepileptic drug therapy
Sebahattin Vurucu,Erkan Demirkaya,Mustafa Kul,Bülent Ünay,Davut Gül,Rıdvan Akin,Erdal Gökçay +6 more
TL;DR: C677T variants of MTHFR gene have no contribution in hyperhomocysteinemia in epileptic patients receiving CBZ or VPA, and there are no significant differences among them.
32