Misunderstood about Obesity, Sleep Apnea and Metabolic Syndrome in Adolescents

per Erdim, Ibrahim, Akcay, Teoman, Yildiz, Melek
Publicat a J Clin Sleep Med (2016)

Is Metabolic Syndrome Associated with Obstructive Sleep Apnea in Obese Adolescents?

per Erdim, Ibrahim, Akcay, Teoman, Yilmazer, Rasim, Erdur, Omer, Kayhan, Fatma Tulin
Publicat a J Clin Sleep Med (2015)

Distribution of α-actinin-3 rs1815739 and angiotensin-1 converting enzyme InDel polymorphisms in Turkish bodybuilders

per Polat, Tolga, Dogan, Canan Sercan, Dogan, Murat, Akçay, Teoman, Ulucan, Korkut
Publicat a Biomed Rep (2020)

Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib

per Turan, Serap, Akin, Leyla, Akcay, Teoman, Adal, Erdal, Sarikaya, Sevil, Bastepe, Murat, Jüppner, Harald
Publicat 2010

Transient Neonatal Diabetes Mellitus in a Turkish Patient with Three Novel Homozygous Variants in the ZFP57 Gene

per Boyraz, Mehmet, Ulucan, Korkut, Taşkın, Necati, Akçay, Teoman, Flanagan, Sarah E., Mackay, Deborah J.G.
Publicat 2013

Constitutional Growth Delay Pattern of Growth in Velo−Cardio−Facial Syndrome: Longitudinal follow up and final height of two cases

per Turan, Serap, Özdemir, Nihal, Güran, Tülay, Akalın, Figen, Akçay, Teoman, Ayabakan, Canan, Yılmaz, Yüksel, Bereket, Abdullah
Publicat 2008

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatasez-scores in Different Types of Rickets

per Turan, Serap, Topcu, Burcu, Gökçe, Ibrahim, Güran, Tülay, Atay, Zeynep, Omar, Anjumanara, Akçay, Teoman, Bereket, Abdullah
Publicat 2011

Effects of ACE Inhibitors on Insulin Resistance and Lipid Profile in Children with Metabolic Syndrome

per Çelebi Bitkin, Eda, Boyraz, Mehmet, Taşkın, Necati, Akçay, Arzu, Ulucan, Korkut, Akyol, Mehmet Bedir, Akçay, Teoman
Publicat 2013

Identification of a Novel Dentin Matrix Protein-1 (DMP-1) Mutation and Dental Anomalies in a Kindred with Autosomal Recessive Hypophosphatemia

per Turan, Serap, Aydin, Cumhur, Bereket, Abdullah, Akcay, Teoman, Güran, Tülay, Yaralioglu, Betul Akmen, Bastepe, Murat, Jüppner, Harald
Publicat 2009

Circulating Insulin-like Growth Factor Binding Protein-4 (IGFBP-4) is not Regulated by Parathyroid Hormone and Vitamin D in vivo: Evidence from Children with Rickets

per Bereket, Abdullah, Cesur, Yaşar, Özkan, Behzat, Adal, Erdal, Turan, Serap, Hanedan Onan, Sertaç, Döneray, Hakan, Akçay, Teoman, Haklar, Goncagül
Publicat 2010

Association Between Endocrine Diseases and Serous Otitis Media in Children

per Koçyiğit, Murat, Çakabay, Taliye, Örtekin, Safiye G., Akçay, Teoman, Özkaya, Güven, Üstün Bezgin, Selin, Yıldız, Melek, Adalı, Mustafa Kemal
Publicat a J Clin Res Pediatr Endocrinol (2017)

Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase

per Heslegrave, Amanda J, Kapoor, Ritika R, Eaton, Simon, Chadefaux, Bernadette, Akcay, Teoman, Simsek, Enver, Flanagan, Sarah E, Ellard, Sian, Hussain, Khalid
Publicat 2012

Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism

per Weger, Meltem, Weger, Benjamin D., Görling, Benjamin, Poschet, Gernot, Yildiz, Melek, Hell, Rüdiger, Luy, Burkhard, Akcay, Teoman, Güran, Tülay, Dickmeis, Thomas, Müller, Ferenc, Krone, Nils
Publicat a EBioMedicine (2018)

Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees

per Flanagan, Sarah E., Patch, Ann-Marie, Locke, Jonathan M., Akcay, Teoman, Simsek, Enver, Alaei, Mohammadreza, Yekta, Zeinab, Desai, Meena, Kapoor, Ritika R., Hussain, Khalid, Ellard, Sian
Publicat 2011

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

per Arman, Ahmet, Bereket, Abdullah, Coker, Ajda, Kiper, Pelin Özlem Şimşek, Güran, Tülay, Özkan, Behzat, Atay, Zeynep, Akçay, Teoman, Haliloglu, Belma, Boduroglu, Koray, Alanay, Yasemin, Turan, Serap
Publicat 2014

The Use of Social Network in Daily Pediatric Practice and Education: Turkish Pediatric Atelier

per Gönüllü, Erdem, Soysal, Ahmet, Can, İlkay, Tutak, Ercan, Tunç, Turan, Yıldız, İsmail, Yeşilbaş, Osman, Öner, Naci, Anarat, Ali, Soysal, Feryal Gün, Bayram, Cengiz, Balcı, Mehmet Cihan, Tavil, Emine Betül, Akçay, Teoman, Karaböcüoğlu, Metin
Publicat a Int J Pediatr (2020)

Hypogonadotropic Hypogonadism due to a Novel Missense Mutation in the First Extracellular Loop of the Neurokinin B Receptor

per Guran, Tulay, Tolhurst, Gwen, Bereket, Abdullah, Rocha, Nuno, Porter, Keith, Turan, Serap, Gribble, Fiona M., Kotan, L. Damla, Akcay, Teoman, Atay, Zeynep, Canan, Husniye, Serin, Ayse, O’Rahilly, Stephen, Reimann, Frank, Semple, Robert K., Topaloglu, A. Kemal
Publicat a J Clin Endocrinol Metab (2009)

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

per 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
Publicat 2013

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia

per Schlingmann, Karl P., Ruminska, Justyna, Kaufmann, Martin, Dursun, Ismail, Patti, Monica, Kranz, Birgitta, Pronicka, Ewa, Ciara, Elzbieta, Akcay, Teoman, Bulus, Derya, Cornelissen, Elisabeth A.M., Gawlik, Aneta, Sikora, Przemysław, Patzer, Ludwig, Galiano, Matthias, Boyadzhiev, Veselin, Dumic, Miroslav, Vivante, Asaf, Kleta, Robert, Dekel, Benjamin, Levtchenko, Elena, Bindels, René J., Rust, Stephan, Forster, Ian C., Hernando, Nati, Jones, Glenville, Wagner, Carsten A., Konrad, Martin
Publicat a J Am Soc Nephrol (2016)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

per Poyrazoğlu, Şükran, Akçay, Teoman, Arslanoğlu, İlknur, Atabek, Mehmet Emre, Atay, Zeynep, Berberoğlu, Merih, Bereket, Abdullah, Bideci, Aysun, Bircan, İffet, Böber, Ece, Can, Şule, Cesur, Yaşar, Darcan, Şükran, Demir, Korcan, Dündar, Bumin, Ersoy, Betül, Esen, İhsan, Güven, Ayla, Kara, Cengiz, Keskin, Mehmet, Kurtoğlu, Selim, Memioğlu, Nihal, Özbek, Mehmet Nuri, Özgen, Tolga, Sarı, Erkan, Şıklar, Zeynep, Şimşek, Enver, Turan, Serap, Yeşilkaya, Ediz, Yüksel, Bilgin, Darendeliler, Feyza
Publicat a J Clin Res Pediatr Endocrinol (2015)