Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey von Siklar, Zeynep, Berberoglu, Merih

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Evaluation of quality of life in children with precocious puberty von Yılmazer, İlkay N., Abseyi, Sema Nilay, Şenyazar, Gizem, Berberoğlu, Merih, Şıklar, Zeynep, Aycan, Zehra

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Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics von Patel, Kashyap A., Ozbek, Mehmet N., Yildiz, Melek, Guran, Tulay, Kocyigit, Cemil, Acar, Sezer, Siklar, Zeynep, Atar, Muge, Colclough, Kevin, Houghton, Jayne, Johnson, Matthew B., Ellard, Sian, Flanagan, Sarah E., Cizmecioglu, Filiz, Berberoglu, Merih, Demir, Korcan, Catli, Gonul, Bas, Serpil, Akcay, Teoman, Demirbilek, Huseyin, Weedon, Michael N., Hattersley, Andrew T.

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Determining the risk of diabulimia and its relationship with diet quality and nutritional status of adolescents with type 1 diabetes von Şahin-Bodur, Gülsüm, Keser, Alev, Şıklar, Zeynep, Berberoğlu, Merih

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Hyperprolactinemia in children and adolescents and long-term follow-up results of prolactinoma cases: a single-centre experience von Kontbay, Tugba, Siklar, Zeynep, Ozsu, Elif, Uyanik, Rukiye, Bilici, Esra, Ceran, Aysegul, Berberoglu, Merih

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Precocious puberty and normal variant puberty: definition, etiology, diagnosis and current management von Berberoğlu, Merih

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Intrathyroidal Ectopic Thymus in Children: Retrospective Analysis of Grayscale and Doppler Sonographic Features von Yildiz, Adalet Elcin, Ceyhan, Koray, Sıklar, Zeynep, Bilir, Pelin, Yağmurlu, Emin Aydın, Berberoğlu, Merih, Fitoz, Suat

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Investigation of early puberty prevalence and time of addition thelarche to pubarche in girls with premature pubarche: two-year follow-up results von Olgun, Esin Gizem, Cetin, Sirmen Kizilcan, Siklar, Zeynep, Aycan, Zehra, Ozsu, Elif, Ceran, Aysegul, Berberoglu, Merih

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Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation von Flanagan, Sarah E., Xie, Weijia, Caswell, Richard, Damhuis, Annet, Vianey-Saban, Christine, Akcay, Teoman, Darendeliler, Feyza, Bas, Firdevs, Guven, Ayla, Siklar, Zeynep, Ocal, Gonul, Berberoglu, Merih, Murphy, Nuala, O’Sullivan, Maureen, Green, Andrew, Clayton, Peter E., Banerjee, Indraneel, Clayton, Peter T., Hussain, Khalid, Weedon, Michael N., Ellard, Sian

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The Relationship Between Diet Quality of Adolescents with Type 1 Diabetes and Nutritional Status and Biochemical Parameters von Gülsüm Şahin Bodur, Keser, Alev, Sıklar, Zeynep, Berberoğlu, Merih

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MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation von Garg, Nisha, MD candidate, Bademci, Guney, MD, Foster, Joseph, BSc, Sıklar, Zeynep, MD, Berberoglu, Merih, MD, Tekin, Mustafa, MD

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Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up von Cetin, Sirmen Kizilcan, Siklar, Zeynep, Ozsu, Elif, Aycan, Zehra, Uyanik, Rukiye, Bilici, Meliha E., Ceran, Aysegul, Berberoglu, Merih

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Syndromic disorders with short stature von Şıklar, Zeynep, Berberoğlu, Merih

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Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b von Hwa, Vivian, Little, Brian, Adiyaman, Pelin, Kofoed, Eric M., Pratt, Katherine L., Ocal, Gonul, Berberoglu, Merih, Rosenfeld, Ron G.

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ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity von Kocaay, Pınar, Şıklar, Zeynep, Çamtosun, Emine, Kendirli, Tanıl, Berberoğlu, Merih

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Difficulties in the diagnosis and management of eight infants with secondary pseudohypoaldosteronism von Gunay, Fatih, Siklar, Zeynep, Berberoglu, Merih

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Intrathyroidal Ectopic Thymus in Children von Yildiz, Adalet Elcin, Ceyhan, Koray, Sıklar, Zeynep, Bilir, Pelin, Yağmurlu, Emin Aydın, Berberoğlu, Merih, Fitoz, Suat

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A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course von Çamtosun, Emine, Flanagan, Sarah E, Ellard, Sian, Şıklar, Zeynep, Hussain, Khalid, Kocaay, Pınar, Berberoğlu, Merih

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Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum von Taylan, Fulya, Costantini, Alice, Coles, Nicole, Pekkinen, Minna, Héon, Elise, Şıklar, Zeynep, Berberoğlu, Merih, Kämpe, Anders, Kıykım, Ertuğrul, Grigelioniene, Giedre, Tüysüz, Beyhan, Mäkitie, Outi

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Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters von Şıklar, Zeynep, Öçal, Gönül, Berberoğlu, Merih, Hacıhamdioğlu, Bülent, Erdeve, Şenay Savas, Eğin, Yonca, Akar, Nejat

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