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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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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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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The Role of American Thyroid Association Pediatric Thyroid Cancer Risk Stratification and BRAFV600E Mutation in Predicting the Response to Treatment in Papillary Thyroid Cancer Pat... von Giles Şenyürek, Yasemin, İşcan, Yalın, Sormaz, İsmail Cem, Poyrazoğlu, Şükran, Tunca, Fatih

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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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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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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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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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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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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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Long-term Follow-up of a Toddler with Papillary Thyroid Carcinoma: A Case Report with a Literature Review of Patients Under 5 Years of Age von Öztürk, Ayşe Pınar, Karakılıç Özturan, Esin, Gün Soysal, Feryal, Ünal, Seher, Işık, Göknur, Yegen, Gülçin, Önder, Semen, Yıldız, Melek, Poyrazoğlu, Şükran, Baş, Firdevs, Darendeliler, Feyza

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A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutat... von Kardelen, Aslı Derya, Toksoy, Güven, Baş, Firdevs, Yavaş Abalı, Zehra, Gençay, Genco, Poyrazoğlu, Şükran, Bundak, Rüveyde, Altunoğlu, Umut, Avcı, Şahin, Najaflı, Adam, Uyguner, Oya, Karaman, Birsen, Başaran, Seher, Darendeliler, Feyza

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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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Body proportions in patients with Turner syndrome on growth hormone treatment von AL, ASLI DERYA KARDELEN, ŞÜKÜR, NUR MİNE, ÖZTURAN, ESİN KARAKILIÇ, ÖZTÜRK, AYŞE PINAR, POYRAZOĞLU, ŞÜKRAN, BAŞ, FİRDEVS, DARENDELİLER, FATMA FEYZA

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Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor von Aycan, Zehra, Keskin, Melikşah, Lafcı, Naz Güleray, Savaş-Erdeve, Şenay, Baş, Firdevs, Poyrazoğlu, Şükran, Öztürk, Pınar, Parlak, Mesut, Ercan, Oya, Güran, Tülay, Hatipoğlu, Nihal, Uçaktürk, Seyit Ahmet, Çatlı, Gönül, Akyürek, Nesibe, Önder, Aşan, Kılınç, Suna, Çetinkaya, Semra

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Oral Bacteria of Children with Turner Syndrome von Unsal, Gulcan, Topcuoglu, Nursen, Guven, Yeliz, Poyrazoglu, Sukran, Kulekci, Guven, Aktoren, Oya

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Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia von Savas-Erdeve, Senay, Aycan, Zehra, Cetinkaya, Semra, Ozturk, Ayse Pinar, Bas, Firdevs, Poyrazoglu, Sukran, Darendeliler, Feyza, Ozsu, Elif, Siklar, Zeynep, Demiral, Meliha, Unal, Edip, Ozbek, Mehmet Nuri, Gurbuz, Fatih, Yuksel, Bilgin, Evliyaoglu, Olcay, Akyurek, Nesibe, Berberoglu, Merih

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