Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation von Dağdeviren Çakır, Aydilek, Turan, Hande, Aykut, Ayça, Durmaz, Asude, Ercan, Oya, Evliyaoğlu, Olcay

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Temporary Thyroid Dysfunction and Catecholamine Excess Due to Mercury Poisoning in 6 Cases von Özer, Yavuz, Yıldız, Mehmet, Turan, Hande, Dağdeviren Çakır, Aydilek, Tarçın, Gürkan, Bingöl Aydın, Dilek, Bayramoğlu, Elvan, Haşlak, Fatih, Şahin, Sezgin, Adrovic, Amra, Barut, Kenan, Evliyaoğlu, Olcay, Kasapçopur, Özgür, Ercan, Oya

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Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome von Cakir, Aydilek Dagdeviren, Bas, Firdevs, Akin, Onur, Siklar, Zeynep, Ozcabi, Bahar, Berberoglu, Merih, Kardelen, Asli Derya, Bayramoglu, Elvan, Poyrazoglu, Sukran, Aydin, Murat, Ergur, Ayca Torel, Goksen, Damla, Bolu, Semih, Aycan, Zehra, Tuysuz, Beyhan, Ercan, Oya, Evliyaoglu, Olcay

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Assessment of Serum Spexin Levels in Obese Adolescents with Metabolic Syndrome Antecedents: Preliminary Results von Kalay Senturk, Nida Gulderen, Dagdeviren Cakir, Aydilek, Yildirmak, Zeynep Yildiz, Ucar, Ahmet

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A Rare Presentation of Homozygous Pathogenic Variant in MC2R Gene with Salt-Wasting Crisis in a Neonate von Kardas Yildiz, Aysenur, Bulbul, Ali, Ozer Bekmez, Buse, Turkyilmaz, Ayberk, Terali, Kerem, Dagdeviren Cakir, Aydilek, Ucar, Ahmet

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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism von Kotan, Leman Damla, Ternier, Gaetan, Cakir, Aydilek Dagdeviren, Emeksiz, Hamdi Cihan, Turan, Ihsan, Delpouve, Gaspard, De Kardelen, Asli rya, Ozcabi, Bahar, Isik, Emregul, Mengen, Eda, De Cakir, Esra niz P., Yuksel, Aysegul, Agladioglu, Sebahat Yilmaz, Dilek, Semine Ozdemir, Evliyaoglu, Olcay, Darendeliler, Feyza, Gurbuz, Fatih, Akkus, Gamze, Yuksel, Bilgin, Giacobini, Paolo, Topaloglu, A. Kemal

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Proteinuria in a patient with Graves’ disease: Answers von Dagdeviren Cakir, Aydilek, Canpolat, Nur, Saygili, Seha, Kilicaslan, Isin, Turan, Hande, Ercan, Oya, Evliyaoglu, Olcay

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Correction: Clinical indicators that influence a clinician’s decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia von Yilmaz, Aslan, Ozer, Yavuz, Kaya, Nesrin, Cakir, Aydilek Dagdeviren, Culpan, Hazal Cansu, Perk, Yildiz, Vural, Mehmet, Evliyaoglu, Olcay

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Elevated Urinary VEGF-A, Transferrin, and Angiotensinogen Levels in Normoalbuminuric Children and Adolescents with Type 1 Diabetes: Can They Be Early Markers of Diabetic Kidney Dis... von Dağdeviren Çakır, Aydilek, Saygılı, Seha Kamil, Canpolat, Nur, Konukoğlu, Dildar, Turan, Hande, Çalışkan, Salim, Sever, Lale, Ercan, Oya, Evliyaoğlu, Olcay

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Differentiated Thyroid Cancer in Children and Adolescents: Clinicopathological Characteristics of 32 Patients Followed up in our Pediatric Endocrinology Unit von Dagdeviren Cakir, Aydilek

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Evaluation of the thyroid disorders in children with familial Mediterranean fever von Turan, Hande, Yildiz, Mehmet, Civan, Orkun, Cakir, Aydilek Dagdeviren, Tarcin, Gurkan, Ozer, Yavuz, Bayramli, Zerengiz, Kucur, Mine, Adaletli, Ibrahim, Adrovic, Amra, Barut, Kenan, Ercan, Oya, Kasapcopur, Ozgur, Evliyaoglu, Saadet Olcay

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Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant von Özer, Yavuz, Turan, Hande, Dağdeviren Çakır, Aydilek, Gökalp, Selman, Ocak, Zeynep, Ercan, Oya, Evliyaoğlu, Olcay

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A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Mullerian Duct Syndrome von Cakir, Aydilek Dagdeviren, Turan, Hande, Tuysuz, Beyhan, Onay, Huseyin, Ercan, Oya, Evliyaoglu, Saadet Olcay

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SUN-624 Occurrence Of Papillary Thyroid Cancer During Treatment Of Thyroid Dysfunction von Ercan, Oya, Dagdeviren Cakır, Aydilek, Emre, Senol, Turan, Hande, Calay, Zerrin, Evliyaoglu, Saadet, Bukey, Yusuf

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A Novel Mutation in AMHR2 Gene in Two Siblings with Persistent Müllerian Duct Syndrome von Aydilek, Dağdeviren Çakır, Turan, Hande, Tüysüz, Beyhan, Onay, Hüseyin, Ercan, Oya, Evliyaoğlu, Saadet Olcay

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Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant von Özer, Yavuz, Turan, Hande, Dağdeviren Çakır, Aydilek, Gökalp, Selman, Ocak, Zeynep, Ercan, Oya, Evliyaoğlu, Olcay

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Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey von Poyrazoğlu, Şükran, Bundak, Rüveyde, Yavaş Abalı, Zehra, Önal, Hasan, Sarıkaya, Sevil, Akgün, Abdurrahman, Baş, Serpil, Abalı, Saygın, Bereket, Abdullah, Eren, Erdal, Tarım, Ömer, Güven, Ayla, Yıldız, Metin, Karaman Aksakal, Derya, Yüksel, Ayşegül, Seymen Karabulut, Gülcan, Hatun, Şükrü, Özgen, Tolga, Cesur, Yaşar, Azizoğlu, Mehmet, Dilek, Emine, Tütüncüler, Filiz, Papatya Çakır, Esra, Özcabı, Bahar, Evliyaoğlu, Olcay, Karadeniz, Songül, Dursun, Fatma, Bolu, Semih, Arslanoğlu, İlknur, Yeşiltepe Mutlu, Gül, Kırmızıbekmez, Heves, İşgüven, Pınar, Üstyol, Ala, Adal, Erdal, Uçar, Ahmet, Cebeci, Nurcan, Bezen, Didem, Binay, Çiğdem, Semiz, Serap, Korkmaz, Hüseyin Anıl, Memioğlu, Nihal, Sağsak, Elif, Peltek, Havva Nur, Yıldız, Melek, Akçay, Teoman, Turan, Serap, Güran, Tülay, Atay, Zeynep, Akcan, Neşe, Çizmecioğlu, Filiz, Ercan, Oya, Dağdeviren, Aydilek, Baş, Firdevs, İşsever, Halim, Darendeliler, Feyza

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