Potential risk factors for vitamin D levels in medium- and long-term use of antiepileptic drugs in childhood von Yildiz, Edibe Pempegül, Poyrazoglu, Şükran, Bektas, Gonca, Kardelen, Aslı Derya, Aydinli, Nur

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Conservative Management of Vaginal Hypoplasia von Dural, Ozlem, Poyrazoglu, Sukran

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Hormone Replacement Therapy in a Patient with Hypogonadism and Coexisting Medical Conditions von Dural, Ozlem, Poyrazoglu, Sukran

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Whole Exome Sequencing Revealed Paternal Inheritance of Obesity-related Genetic Variants in a Family with an Exclusively Breastfed Infant von Olgun Çelebioğlu, Hazal Banu, Öztürk, Ayşe Pınar, Poyrazoğlu, Şükran, Tuncer, Feyza Nur

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Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study von Schröder, Mariska A M, Neacşu, Mihaela, Adriaansen, Bas P H, Sweep, Fred C G J, Ahmed, S Faisal, Ali, Salma R, Bachega, Tânia A S S, Baronio, Federico, Birkebæk, Niels Holtum, de Bruin, Christiaan, Bonfig, Walter, Bryce, Jillian, Clemente, Maria, Cools, Martine, Elsedfy, Heba, Globa, Evgenia, Guran, Tulay, Güven, Ayla, Amr, Nermine Hussein, Janus, Dominika, Taube, Nina Lenherr, Markosyan, Renata, Miranda, Mirela, Poyrazoğlu, Şükran, Rees, Aled, Salerno, Mariacarolina, Stancampiano, Marianna Rita, Vieites, Ana, de Vries, Liat, Yavas Abali, Zehra, Span, Paul N, Claahsen-van der Grinten, Hedi L

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A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent von Poyrazoğlu, Şükran, Hwa, Vivian, Baş, Firdevs, Dauber, Andrew, Rosenfeld, Ron, Darendeliler, Feyza

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A Rare Cause of Adrenal Insufficiency – Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature von Kardelen Al, Aslı Derya, Poyrazoğlu, Şükran, Aslanger, Ayça, Yeşil, Gözde, Ceylaner, Serdar, Baş, Firdevs, Darendeliler, Feyza

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Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey von Karakilic Ozturan, Esin, Ozturk, Ayse Pinar, Bas, Firdevs, Erdogdu, Ayse Burcu, Kaptan, Seven, Kardelen Al, Asli Derya, Poyrazoglu, Sukran, Yıldız, Melek, Direk, Neşe, Yuksel, Sahika, Darendeliler, Feyza

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Two novel mutations in XYLT2 cause spondyloocular syndrome von Taylan, Fulya, Yavaş Abalı, Zehra, Jäntti, Nina, Güneş, Nilay, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Tamçelik, Nevbahar, Tüysüz, Beyhan, Mäkitie, Outi

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A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care von Kardelen, Aslı Derya, Karakılıç Özturan, Esin, Poyrazoğlu, Şükran, Baş, Firdevs, Ceylaner, Serdar, Joustra, Sjoerd D, Wit, Jan M, Darendeliler, Feyza

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Investigating Leptin Gene Variants and Methylation Status in Relation to Breastfeeding and Preventing Obesity von Kilic, Ayse, Pehlivan, Sacide, Varkal, Muhammet Ali, Tuncel, Fatima Ceren, Kandemir, Ibrahim, Ozcetin, Mustafa, Poyrazoglu, Sükran, Kardelen, Asli Derya, Ozdemir, Irem, Yildiz, Ismail

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Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone von Saygılı, Seha, Kocaağa, Mehmet, Kaya, Gamze, Şükür, Mine, Baş, Firdevs, Poyrazoğlu, Şükran, Bundak, Rüveyde, Darendeliler, Feyza

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PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency von Kardelen, Aslı Derya, Najafli, Adam, Baş, Firdevs, Karaman, Birsen, Toksoy, Güven, Poyrazoğlu, Şükran, Avcı, Şahin, Altunoğlu, Umut, Yavaş Abalı, Zehra, Öztürk, Ayşe Pınar, Karakılıç Özturan, Esin, Başaran, Seher, Darendeliler, Feyza, Uyguner, Z Oya

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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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In response to: “Letter to: Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey” von Ozturan, Esin Karakilic, Ozturk, Ayse Pinar, Bas, Firdevs, Erdogdu, Ayse Burcu, Kaptan, Seven, Al, Asli Derya Kardelen, Poyrazoglu, Sukran, Yildiz, Melek, Direk, Nese, Yuksel, Sahika, Darendeliler, Feyza

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Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD von Akcan, Neşe, Uyguner, Oya, Baş, Firdevs, Altunoğlu, Umut, Toksoy, Güven, Karaman, Birsen, Avcı, Şahin, Yavaş Abalı, Zehra, Poyrazoğlu, Şükran, Aghayev, Agharza, Karaman, Volkan, Bundak, Rüveyde, Başaran, Seher, Darendeliler, Feyza

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Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings von Akcan, Neşe, Poyrazoğlu, Şükran, Baş, Firdevs, Bundak, Rüveyde, Darendeliler, Feyza

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Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medicatio... von Neumann, Uta, van der Linde, Annelieke, Krone, Ruth E, Krone, Nils P, Güven, Ayla, Güran, Tülay, Elsedfy, Heba, Poyrazoglu, Sukran, Darendeliler, Feyza, Bachega, Tania A S S, Balsamo, Antonio, Hannema, Sabine E, Birkebaek, Niels, Vieites, Ana, Thankamony, Ajay, Cools, Martine, Milenkovic, Tatjana, Bonfig, Walter, Costa, Eduardo Correa, Atapattu, Navoda, de Vries, Liat, Guaragna-Filho, Guilherme, Korbonits, Marta, Mohnike, Klaus, Bryce, Jillian, Ahmed, S Faisal, Voet, Bernard, Blankenstein, Oliver, Claahsen-van der Grinten, Hedi L

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Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome von Dağdeviren Çakır, Aydilek, Baş, Firdevs, Akın, Onur, Şıklar, Zeynep, Özcabı, Bahar, Berberoğlu, Merih, Kardelen, Aslı Derya, Bayramoğlu, Elvan, Poyrazoğlu, Şükran, Aydın, Murat, Törel Ergür, Ayça, Gökşen, Damla, Bolu, Semih, Aycan, Zehra, Tüysüz, Beyhan, Ercan, Oya, Evliyaoğlu, Olcay

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Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene von Baş, Firdevs, Toksoy, Güven, Ergun-Longmire, Berrin, Uyguner, Zehra Oya, Abalı, Zehra Yavaş, Poyrazoğlu, Şükran, Karaman, Volkan, Avcı, Şahin, Altunoğlu, Umut, Bundak, Ruveyde, Karaman, Birsen, Başaran, Seher, Darendeliler, Feyza

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