Gender Identity and Assignment Recommendations in Disorders of Sex Development (DSD) Patients: 20 years’ Experience and Challenges
Gurbuz, Fatih, Alkan, Murat, Celik, Gonca, Bisgin, Atil, Cekin, Necmi, Unal, Ilker, Topaloglu, Ali Kemal, Zorludemir, Unal, Avci, Ayse, Yuksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.12.2020)
Published in Journal of clinical research in pediatric endocrinology (01.12.2020)
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Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey
Ekinci, Rabia Miray Kisla, Gurbuz, Fatih, Balci, Sibel, Bisgin, Atil, Tastan, Mehmet, Yuksel, Bilgin, Yilmaz, Mustafa
Published in Journal of clinical research in pediatric endocrinology (01.03.2019)
Published in Journal of clinical research in pediatric endocrinology (01.03.2019)
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Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations
Akkuş, Gamze, Kotan, Leman Damla, Durmaz, Erdem, Mengen, Eda, Turan, İhsan, Ulubay, Ayça, Gürbüz, Fatih, Yüksel, Bilgin, Tetiker, Tamer, Topaloğlu, A Kemal
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey
Poyrazoğlu, Şükran, Akçay, Teoman, Arslanoğlu, İlknur, Atabek, Mehmet Emre, Atay, Zeynep, Berberoğlu, Merih, Bereket, Abdullah, Bideci, Aysun, Bircan, İffet, Böber, Ece, Can, Şule, Cesur, Yaşar, Darcan, Şükran, Demir, Korcan, Dündar, Bumin, Ersoy, Betül, Esen, İhsan, Güven, Ayla, Kara, Cengiz, Keskin, Mehmet, Kurtoğlu, Selim, Memioğlu, Nihal, Özbek, Mehmet Nuri, Özgen, Tolga, Sarı, Erkan, Şıklar, Zeynep, Şimşek, Enver, Turan, Serap, Yeşilkaya, Ediz, Yüksel, Bilgin, Darendeliler, Feyza
Published in Journal of clinical research in pediatric endocrinology (01.03.2015)
Published in Journal of clinical research in pediatric endocrinology (01.03.2015)
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Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype
Chong, Belinda, Hegde, Madhuri, Fawkner, Matthew, Simonet, Scott, Cassinelli, Hamilton, Coker, Mahmut, Kanis, John, Seidel, Joerg, Tau, Cristina, Tüysüz, Beyhan, Yüksel, Bilgin, Love, Donald, Cundy, Tim
Published in Journal of bone and mineral research (01.12.2003)
Published in Journal of bone and mineral research (01.12.2003)
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Urolithiasis Frequency and Risk Factors in Home Ventilated Patients with Tracheostomy
Tolunay, İlknur, Yıldızdaş, R. Dinçer, Horoz, Özden Özgür, Melek, Engin, Atmış, Bahriye, Yüksel, Bilgin, Turan, İhsan
Published in Turkish Journal of Pediatric Emergency and Intensive Care Medicine (14.12.2017)
Published in Turkish Journal of Pediatric Emergency and Intensive Care Medicine (14.12.2017)
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Journal Article
Plasma pentraxin‐3 levels and its role in childhood obesity—Is it anti‐inflammatory? A matched group study
Uysal, Merve, Mete, Burak, Kara, Ertan, Demirhindi, Hakan, Haytoglu, Zeliha, Yuksel, Bilgin, Turan, İhsan, Daglioglu, Gülçin, Dogus, Yusuf
Published in Clinical endocrinology (Oxford) (01.07.2024)
Published in Clinical endocrinology (Oxford) (01.07.2024)
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Inactivating KISS1 Mutation and Hypogonadotropic Hypogonadism
Topaloglu, A. Kemal, Tello, Javier A, Kotan, L. Damla, Ozbek, Mehmet N, Yilmaz, M. Bertan, Erdogan, Seref, Gurbuz, Fatih, Temiz, Fatih, Millar, Robert P, Yuksel, Bilgin
Published in The New England journal of medicine (16.02.2012)
Published in The New England journal of medicine (16.02.2012)
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Journal Article
Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey
Dilek, Semine Özdemir, Gürbüz, Fatih, Turan, İhsan, Celiloğlu, Can, Yüksel, Bilgin
Published in Journal of Pediatric Endocrinology & Metabolism (26.10.2021)
Published in Journal of Pediatric Endocrinology & Metabolism (26.10.2021)
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A novel homozygous nonsense NDNF variant in Kallmann syndrome
Kotan, Leman Damla, Yildiz, Melek, Turan, Ihsan, Celiloglu, Can, Yuksel, Bilgin, Topaloglu, Ali Kemal
Published in American journal of medical genetics. Part A (01.03.2023)
Published in American journal of medical genetics. Part A (01.03.2023)
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DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism
Turan, Ihsan, Demir, Korcan, Mengen, Eda, Kotan, Leman Damla, Gürbüz, Fatih, Yüksel, Bilgin, Topaloglu, Ali Kemal
Published in Hormone research in paediatrics (01.02.2022)
Published in Hormone research in paediatrics (01.02.2022)
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Journal Article
TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
Topaloglu, A Kemal, O'Rahilly, Stephen, Reimann, Frank, Guclu, Metin, Yalin, Ayse Serap, Kotan, L Damla, Porter, Keith M, Serin, Ayse, Mungan, Neslihan O, Cook, Joshua R, Ozbek, Mehmet N, Imamoglu, Sazi, Akalin, N Sema, Yuksel, Bilgin, Semple, Robert K
Published in Nature genetics (01.03.2009)
Published in Nature genetics (01.03.2009)
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Journal Article
Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance
Turan, Ihsan, Kotan, Leman Damla, Tastan, Mehmet, Gurbuz, Fatih, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Clinical endocrinology (Oxford) (01.06.2018)
Published in Clinical endocrinology (Oxford) (01.06.2018)
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Kronik karaciğer hastalığı olan çocukların D vitamini düzeyleri
Gürbüz, Fatih, Ağın, Mehmet, Mengen, Eda, Elçi, Hüseyin, Ünal, İlker, Tümgör, Gökhan, Yüksel, Bilgin
Published in Cukurova Medical Journal (31.12.2018)
Published in Cukurova Medical Journal (31.12.2018)
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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
Guran, Tulay, Buonocore, Federica, Saka, Nurcin, Ozbek, Mehmet Nuri, Aycan, Zehra, Bereket, Abdullah, Bas, Firdevs, Darcan, Sukran, Bideci, Aysun, Guven, Ayla, Demir, Korcan, Akinci, Aysehan, Buyukinan, Muammer, Aydin, Banu Kucukemre, Turan, Serap, Agladioglu, Sebahat Yilmaz, Atay, Zeynep, Abali, Zehra Yavas, Tarim, Omer, Catli, Gonul, Yuksel, Bilgin, Akcay, Teoman, Yildiz, Metin, Ozen, Samim, Doger, Esra, Demirbilek, Huseyin, Ucar, Ahmet, Isik, Emregul, Ozhan, Bayram, Bolu, Semih, Ozgen, Ilker Tolga, Suntharalingham, Jenifer P, Achermann, John C
Published in The journal of clinical endocrinology and metabolism (01.01.2016)
Published in The journal of clinical endocrinology and metabolism (01.01.2016)
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Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism
Kotan, Leman D., Isik, Emregul, Turan, Ihsan, Mengen, Eda, Akkus, Gamze, Tastan, Mehmet, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal
Published in Clinical genetics (01.02.2019)
Published in Clinical genetics (01.02.2019)
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CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism
Turan, Ihsan, Hutchins, B. Ian, Hacihamdioglu, Bulent, Kotan, L. Damla, Gurbuz, Fatih, Ulubay, Ayca, Mengen, Eda, Yuksel, Bilgin, Wray, Susan, Topaloglu, A. Kemal
Published in The journal of clinical endocrinology and metabolism (01.06.2017)
Published in The journal of clinical endocrinology and metabolism (01.06.2017)
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Journal Article
Mutations within The Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency
Bulut, Fatma Derya, Özdemir Dilek, Semine, Kotan, Damla, Mengen, Eda, Gürbüz, Fatih, Yüksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.09.2020)
Published in Journal of clinical research in pediatric endocrinology (01.09.2020)
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