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1دورية أكاديمية
المؤلفون: Baş, Firdevs, Darendeliler, Fatma Feyza, Devecioglu, Esra, Poyrazoğlu, Şükran, Gökçay, Emine Gülbin, Aydin, Banu K., Kadioglu, Alev, Kaya, Gamze A.
المساهمون: Uppsala Universitet (Uppsala University) ,, 3389877
مصطلحات موضوعية: Endokrinoloji ve Metabolizma Hastalıkları, Endocrinology, Endocrine and Autonomic Systems, Diabetes and Metabolism, Life Sciences, Health Sciences, Dahili Tıp Bilimleri, İç Hastalıkları, Sağlık Bilimleri, Tıp, Klinik Tıp (MED), Klinik Tıp, ENDOKRİNOLOJİ VE METABOLİZMA
العلاقة: CLINICAL ENDOCRINOLOGY; Aydin B. K. , Kadioglu A., Kaya G. A. , Devecioglu E., Baş F., Poyrazoğlu Ş., Gökçay E. G. , Darendeliler F. F. , "Pelvic and breast ultrasound abnormalities and associated metabolic disturbances in girls with premature pubarche due to adrenarche", CLINICAL ENDOCRINOLOGY, 2021; vv_1032021; av_7c3c2ebd-7b77-4a32-99d6-b7cb309d9aba; http://hdl.handle.net/20.500.12627/178590Test; https://doi.org/10.1111/cen.14662Test
الإتاحة: https://doi.org/20.500.12627/178590Test
https://doi.org/10.1111/cen.14662Test
https://hdl.handle.net/20.500.12627/178590Test -
2دورية أكاديمية
المؤلفون: Aydin, Banu K., Bas, Firdevs, Isbir, Turgay, Timirci, Ozlem, Kelesoglu, Fatih, Eryilmaz, Sema Kabatas, Darendeliler, Feyza F., Bozkurt, Nilufer, Bundak, Ruveyde, Saka, Nurcin H., Gunoz, Hulya
المساهمون: İstanbul Üniversitesi ,
مصطلحات موضوعية: Klinik Tıp, Klinik Tıp (MED), Tıp, ENDOKRİNOLOJİ VE METABOLİZMA, İç Hastalıkları, Endokrinoloji ve Metabolizma Hastalıkları, Sağlık Bilimleri, Dahili Tıp Bilimleri
العلاقة: HORMONE RESEARCH; Bas F., Kelesoglu F., Eryilmaz S. K. , Darendeliler F. F. , Aydin B. K. , Timirci O., Bozkurt N., Bundak R., Saka N. H. , Gunoz H., et al., "The distribution of exon 3-deleted/full-length growth hormone receptor polymorphism in Turkish population", HORMONE RESEARCH, cilt.72, ss.87, 2009; vv_1032021; av_e3bc44f1-215d-4fba-b018-0caf08e3ced4; http://hdl.handle.net/20.500.12627/149844Test; 72; 87
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3دورية أكاديمية
المؤلفون: Aydin, Banu K., Cesur, Yasar, Kurtoglu, Selim, Bas, Veysel, EREN, ERDAL, DEMİR, KORCAN, Kiraz, Aslihan, Maher, Eamonn R., Barrett, Timothy G., Hoegler, Wolfgang, Kirk, Jeremy, Shaw, Nick J., Boelaert, Kristien, Kendall, Michaela, Darendeliler, Feyza, Karthikeyan, Ambika, Cangul, Hakan, Aycan, Zehra, Saglam, Halil, Forman, Julia R., Cetinkaya, Semra, Tarim, Omer, BÖBER, ECE
المساهمون: University Of Birmingham ,, 204576
مصطلحات موضوعية: Dahili Tıp Bilimleri, Sağlık Bilimleri, Tıp, Çocuk Sağlığı ve Hastalıkları, İç Hastalıkları, PEDİATRİ, Klinik Tıp (MED), Klinik Tıp, ENDOKRİNOLOJİ VE METABOLİZMA, Endokrinoloji ve Metabolizma Hastalıkları
العلاقة: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM; Cangul H., Aycan Z., Saglam H., Forman J. R. , Cetinkaya S., Tarim O., BÖBER E., Cesur Y., Kurtoglu S., Darendeliler F., et al., "TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.25, ss.419-426, 2012; vv_1032021; av_ee6645e0-50b1-4d42-bdae-e585088b16fa; http://hdl.handle.net/20.500.12627/156501Test; https://doi.org/10.1515/jpem-2012-0053Test; 25; 419; 426
الإتاحة: https://doi.org/20.500.12627/156501Test
https://doi.org/10.1515/jpem-2012-0053Test
https://hdl.handle.net/20.500.12627/156501Test -
4دورية أكاديمية
المؤلفون: Olivera-Nappa, Alvaro, Bas, Veysel, DEMİR, KORCAN, Kendall, Michaela, Cole, Trevor, Hoegler, Wolfgang, Chatterjee, V. Krishna K., Barrett, Timothy G., Maher, Eamonn R., Darendeliler, Fatma Feyza, Aydin, Banu K., Cangul, Hakan, Aycan, Zehra, Saglam, Halil, Schoenmakers, Nadia A., Boelaert, Kristien, Cetinkaya, Semra, Tarim, Omer, BÖBER, ECE
المساهمون: İstanbul Üniversitesi ,, 210408
مصطلحات موضوعية: Endocrine and Autonomic Systems, ENDOKRİNOLOJİ VE METABOLİZMA, Klinik Tıp, Klinik Tıp (MED), Tıp, Sağlık Bilimleri, Dahili Tıp Bilimleri, İç Hastalıkları, Endokrinoloji ve Metabolizma Hastalıkları, Endocrinology, Diabetes and Metabolism, Life Sciences, Health Sciences
العلاقة: CLINICAL ENDOCRINOLOGY; Cangul H., Aycan Z., Olivera-Nappa A., Saglam H., Schoenmakers N. A. , Boelaert K., Cetinkaya S., Tarim O., BÖBER E., Darendeliler F. F. , et al., "Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community", CLINICAL ENDOCRINOLOGY, cilt.79, ss.275-281, 2013; vv_1032021; av_fb39584d-e9ee-4335-a49a-ecb22f4c247a; http://hdl.handle.net/20.500.12627/164475Test; https://doi.org/10.1111/cen.12127Test; 79; 275; 281
الإتاحة: https://doi.org/20.500.12627/164475Test
https://doi.org/10.1111/cen.12127Test
https://hdl.handle.net/20.500.12627/164475Test