Hyperthyroidism in pediatric patients in a university hospital: Ten years of experience von Kocabey Sütçü,Zümrüt, Selver Eklioğu,Beray, Atabek,Mehmet Emre

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Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study von Şıklar, Zeynep, Özsu, Elif, Kızılcan Çetin, Sirmen, Özen, Samim, Çizmecioğlu-Jones, Filiz, Balkı, Hanife Gül, Aycan, Zehra, Gökşen, Damla, Kilci, Fatih, Abseyi, Sema Nilay, Tercan, Ummahan, Gürpınar, Gözde, Poyrazoğlu, Şükran, Darendeliler, Feyza, Demir, Korcan, Besci, Özge, Özgen, İlker Tolga, Akın, Semra Bahar, Kocabey Sütçü, Zümrüt, Aykaç Kaplan, Emel Hatun, Çamtosun, Emine, Dündar, İsmail, Sağsak, Elif, Korkmaz, Hüseyin Anıl, Anık, Ahmet, Yeşiltepe Mutlu, Gül, Özcabi, Bahar, Uçar, Ahmet, Dağdeviren Çakır, Aydilek, Selver Eklioğlu, Beray, Kırel, Birgül, Berberoğlu, Merih

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Hyperthyroidism in Pediatric Patients in a University Hospital: Ten Years of Experience: Hyperthyroidism in Pediatric Patients von Kocabey Sütçü, Zümrüt, Selver Eklioğlu, Beray, Atabek, Mehmet Emre

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Clinical and genetic characteristics of patients with monocarboxylate transporter-8 deficiency: a multicentre retrospective study von Çelik, Nurullah, Demir, Korcan, Dibeklioğlu, Saime Ergen, Dündar, Bumin Nuri, Hatipoğlu, Nihal, Mutlu, Gül Yeşiltepe, Arslan, Emrullah, Yıldırımçakar, Didem, Çayır, Atilla, Hacıhamdioğlu, Bülent, Sütçü, Zümrüt Kocabey, Ünsal, Yağmur, Karagüzel, Gülay

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Serum Neudesin Levels in Patients with Congenital Hypothyroidism von Bahar, Semra, Özgen, İlker Tolga, Cesur, Yaşar, Yıldız, Caner, Özer, Ömer Faruk, Aytaç Kaplan, Emel Hatun, Kocabey Sütçü, Zümrüt

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Pediatric hypoparathyroidism: etiological and clinical evaluation in a tertiary center von Kocabey Sütçü, Zümrüt, Aytaç Kaplan, Emel Hatun, Önal, Hasan

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Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach von Şıklar, Zeynep, Özsu, Elif, Kızılcan Çetin, Sirmen, Özen, Samim, Çizmecioğlu-Jones, Filiz, Gül Balkı, Hanife, Aycan, Zehra, Goksen, Damla, Kilci, Fatih, Abseyi, Sema Nilay, Tercan, Ummahan, Gürpınar, Gözde, Poyrazoğlu, Şükran, Darendeliler, Feyza, Demir, Korcan, Besci, Özge, Özgen, İlker Tolga, Akın, Semra Bahar, Kocabey Sütçü, Zümrüt, Aykaç Kaplan, Emel Hatun, Çamtosun, Emine, Dundar, İsmail, Sağsak, Elif, Korkmaz, Hüseyin Anıl

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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort von Siklar, Zeynep, Camtosun, Emine, Bolu, Semih, Yildiz, Melek, Akinci, Aysehan, Bas, Firdevs, Dündar, İsmail, Bestas, Asli, Ünal, Edip, Kocaay, Pinar, Guran, Tulay, Buyukyilmaz, Gonul, Ugurlu, Aylin Kilinc, Tosun, Buşra Gurpinar, Turan, Ihsan, Kurnaz, Erdal, Yuksel, Bilgin, Turkkahraman, Doga, Cayir, Atilla, Celmeli, Gamze, Gonc, E. Nazli, Eklioğlu, Beray Selver, Cetinkaya, Semra, Yilmaz, Seniha Kiremitci, Atabek, Mehmet Emre, Buyukinan, Muammer, Arslan, Emrullah, Mengen, Eda, Cakir, Esra Deniz Papatya, Karaoglan, Murat, Hatipoglu, Nihal, Orbak, Zerrin, Ucar, Ahmet, Akyurek, Nesibe, Akbas, Emine Demet, Isik, Emregül, Kaygusuz, Sare Betul, Sutcu, Zumrut Kocabey, Seymen, Gulcan, Berberoglu, Merih

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