Sertoli cell only syndrome with ambiguous genitalia
Gurbuz, Fatih, Ceylaner, Serdar, Erdogan, Seyda, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Journal of Pediatric Endocrinology & Metabolism (01.07.2016)
Published in Journal of Pediatric Endocrinology & Metabolism (01.07.2016)
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Journal Article
Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide
Mengen, Eda, Tunc, Selma, Kotan, L Damla, Nalbantoglu, Ozlem, Demir, Korcan, Gurbuz, Fatih, Turan, Ihsan, Seker, Gül, Yuksel, Bilgin, Topaloglu, A Kemal
Published in Hormone research in paediatrics (01.01.2016)
Published in Hormone research in paediatrics (01.01.2016)
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Journal Article
Evaluation of permanent growth hormone deficiency (GHD) in young adults with childhood onset GHD: a multicenter study
Berberoğlu, Merih, Sıklar, Zeynep, Darendeliler, Feyza, Poyrazoğlu, Sükran, Darcan, Sükran, Işgüven, Pınar, Bideci, Aysun, Ocal, Gönül, Bundak, Rüveyde, Yüksel, Bilgin, Arslanoğlu, Ilknur
Published in Journal of clinical research in pediatric endocrinology (2008)
Published in Journal of clinical research in pediatric endocrinology (2008)
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Journal Article
Isolated Hypoaldosteronism: A Case Report
Turan, Ihsan, Gurbuz, Fatih, Tasdan, Mehmet, Kotan, Leman Damla, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
Journal Article
Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS 1R gene in three unrelated families
Demirbilek, Huseyin, Ozbek, M. Nuri, Demir, Korcan, Kotan, L. Damla, Cesur, Yasar, Dogan, Murat, Temiz, Fatih, Mengen, Eda, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal
Published in Clinical endocrinology (Oxford) (01.03.2015)
Published in Clinical endocrinology (Oxford) (01.03.2015)
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Journal Article
Hashimoto's encephalopathy: four cases and review of literature
Gul Mert, Gülen, Horoz, Ozden Ozgur, Herguner, M. Ozlem, Incecik, Faruk, Yildizdas, R. Dincer, Onenli Mungan, Neslihan, Yuksel, Bilgin, Altunbasak, Sakir
Published in International journal of neuroscience (01.04.2014)
Published in International journal of neuroscience (01.04.2014)
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Journal Article
Serum IL-1, IL-2, TNFalpha and INFgamma levels of patients with type 1 diabetes mellitus and their siblings
Ozer, Güler, Teker, Zeliha, Cetiner, Salih, Yilmaz, Mustafa, Topaloglu, Ali Kemal, Onenli-Mungan, Neslihan, Yüksel, Bilgin
Published in Journal of pediatric endocrinology & metabolism : JPEM (01.02.2003)
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Published in Journal of pediatric endocrinology & metabolism : JPEM (01.02.2003)
Journal Article
Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing
Maharaj, Avinaash, Buonocore, Federica, Meimaridou, Eirini, Ruiz-Babot, Gerard, Guasti, Leonardo, Peng, Hwei-Ming, Capper, Cameron P, Burgos-Tirado, Neikelyn, Prasad, Rathi, Hughes, Claire R, Maudhoo, Ashwini, Crowne, Elizabeth, Cheetham, Timothy D, Brain, Caroline E, Suntharalingham, Jenifer P, Striglioni, Niccolò, Yuksel, Bilgin, Gurbuz, Fatih, Gupta, Sangay, Lindsay, Robert, Couch, Robert, Spoudeas, Helen A, Guran, Tulay, Johnson, Stephanie, Fowler, Dallas J, Conwell, Louise S, McInerney-Leo, Aideen M, Drui, Delphine, Cariou, Bertrand, Lopez-Siguero, Juan P, Harris, Mark, Duncan, Emma L, Hindmarsh, Peter C, Auchus, Richard J, Donaldson, Malcolm D, Achermann, John C, Metherell, Louise A
Published in Journal of the Endocrine Society (01.01.2019)
Published in Journal of the Endocrine Society (01.01.2019)
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Journal Article
Type II hyperprolinemia: a case report
Onenli-Mungan, Neslihan, Yüksel, Bilgin, Elkay, Mürüvet, Topaloğlu, Ali Kemal, Baykal, Tolunay, Ozer, Güler
Published in Turkish journal of pediatrics (01.04.2004)
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Published in Turkish journal of pediatrics (01.04.2004)
Journal Article
Turner syndrome and associated problems in Turkish children: a multicenter study
Yeşilkaya, Ediz, Bereket, Abdullah, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Küçükemre Aydın, Banu, Darcan, Şükran, Dündar, Bumin, Büyükinan, Muammer, Kara, Cengiz, Sarı, Erkan, Adal, Erdal, Akıncı, Ayşehan, Atabek, Mehmet Emre, Demirel, Fatma, Çelik, Nurullah, Özkan, Behzat, Özhan, Bayram, Orbak, Zerrin, Ersoy, Betül, Doğan, Murat, Ataş, Ali, Turan, Serap, Gökşen, Damla, Tarım, Ömer, Yüksel, Bilgin, Ercan, Oya, Hatun, Şükrü, Şimşek, Enver, Ökten, Ayşenur, Abacı, Ayhan, Döneray, Hakan, Özbek, Mehmet Nuri, Keskin, Mehmet, Önal, Hasan, Akyürek, Nesibe, Bulan, Kezban, Tepe, Derya, Emeksiz, Hamdi Cihan, Demir, Korcan, Kızılay, Deniz, Topaloğlu, Ali Kemal, Eren, Erdal, Özen, Samim, Abalı, Saygın, Akın, Leyla, Selver Eklioğlu, Beray, Kaba, Sultan, Anık, Ahmet, Baş, Serpil, Ünüvar, Tolga, Sağlam, Halil, Bolu, Semih, Özgen, Tolga, Doğan, Durmuş, Deniz Çakır, Esra, Şen, Yaşar, Andıran, Nesibe, Çizmecioğlu, Filiz, Evliyaoğlu, Olcay, Karagüzel, Gülay, Pirgon, Özgür, Çatlı, Gönül, Can, Hatice Dilek, Gürbüz, Fatih, Binay, Çiğdem, Baş, Veysel Nijat, Fidancı, Kürşat, Polat, Adem, Gül, Davut, Açıkel, Cengizhan, Demirbilek, Hüseyin, Cinaz, Peyami, Bondy, Carolyn
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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Journal Article
Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature
Ozbek, M Nuri, Senée, Valérie, Aydemir, Sehnaz, Kotan, L Damla, Mungan, Neslihan O, Yuksel, Bilgin, Julier, Cécile, Topaloglu, A Kemal
Published in Pediatric diabetes (01.06.2010)
Published in Pediatric diabetes (01.06.2010)
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Journal Article
Familial thyroxin-binding globulin excess with ichthyosis: a case report
Onenli-Mungan, Neslihan, Yüksel, Bilgin, Ozer, Güler, Denli, Gül, Topaloğlu, Ali Kemal, Teker, Zeliha
Published in Turkish journal of pediatrics (01.04.2004)
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Published in Turkish journal of pediatrics (01.04.2004)
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