Misunderstood about Obesity, Sleep Apnea and Metabolic Syndrome in Adolescents

Por Erdim, Ibrahim, Akcay, Teoman, Yildiz, Melek
Publicado no J Clin Sleep Med (2016)

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

Por Erdim, Ibrahim, Akcay, Teoman, Yilmazer, Rasim, Erdur, Omer, Kayhan, Fatma Tulin
Publicado no J Clin Sleep Med (2015)

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

Por Turan, Serap, Akin, Leyla, Akcay, Teoman, Adal, Erdal, Sarikaya, Sevil, Bastepe, Murat, Jüppner, Harald
Publicado em 2010

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

Por Boyraz, Mehmet, Ulucan, Korkut, Taşkın, Necati, Akçay, Teoman, Flanagan, Sarah E., Mackay, Deborah J.G.
Publicado em 2013

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

Por Turan, Serap, Özdemir, Nihal, Güran, Tülay, Akalın, Figen, Akçay, Teoman, Ayabakan, Canan, Yılmaz, Yüksel, Bereket, Abdullah
Publicado em 2008

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

Por Turan, Serap, Topcu, Burcu, Gökçe, Ibrahim, Güran, Tülay, Atay, Zeynep, Omar, Anjumanara, Akçay, Teoman, Bereket, Abdullah
Publicado em 2011

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

Por Çelebi Bitkin, Eda, Boyraz, Mehmet, Taşkın, Necati, Akçay, Arzu, Ulucan, Korkut, Akyol, Mehmet Bedir, Akçay, Teoman
Publicado em 2013

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

Por Turan, Serap, Aydin, Cumhur, Bereket, Abdullah, Akcay, Teoman, Güran, Tülay, Yaralioglu, Betul Akmen, Bastepe, Murat, Jüppner, Harald
Publicado em 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

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

Association Between Endocrine Diseases and Serous Otitis Media in Children

Por Koçyiğit, Murat, Çakabay, Taliye, Örtekin, Safiye G., Akçay, Teoman, Özkaya, Güven, Üstün Bezgin, Selin, Yıldız, Melek, Adalı, Mustafa Kemal
Publicado no J Clin Res Pediatr Endocrinol (2017)

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

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

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

Por 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
Publicado em 2011

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

Por 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
Publicado em 2014

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

Por 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
Publicado no J Clin Endocrinol Metab (2009)

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

Por 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
Publicado em 2013

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

Por 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
Publicado no J Am Soc Nephrol (2016)

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

Por 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
Publicado no J Clin Res Pediatr Endocrinol (2015)

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Por Guran, Tulay, Buonocore, Federica, Saka, Nurcin, Ozbek, Mehmet Nuri, Aycan, Zehra, Bereket, Abdullah, Bas, Firdevs, Darcan, Sukran, Bideci, Aysun, Guven, Ayla, Demir, Korcan, Akinci, Aysehan, Buyukinan, Muammer, Aydin, Banu Kucukemre, Turan, Serap, Agladioglu, Sebahat Yilmaz, Atay, Zeynep, Abali, Zehra Yavas, Tarim, Omer, Catli, Gonul, Yuksel, Bilgin, Akcay, Teoman, Yildiz, Metin, Ozen, Samim, Doger, Esra, Demirbilek, Huseyin, Ucar, Ahmet, Isik, Emregul, Ozhan, Bayram, Bolu, Semih, Ozgen, Ilker Tolga, Suntharalingham, Jenifer P., Achermann, John C.
Publicado no J Clin Endocrinol Metab (2016)

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

Por Raimondo, Anne, Chakera, Ali J., Thomsen, Soren K., Colclough, Kevin, Barrett, Amy, De Franco, Elisa, Chatelas, Alisson, Demirbilek, Huseyin, Akcay, Teoman, Alawneh, Hussein, Flanagan, Sarah E., Van De Bunt, Martijn, Hattersley, Andrew T., Gloyn, Anna L., Ellard, Sian, Abduljabbar, Mohammad A., Al-Zyoud, Mahmoud, Aman, Syed, Bath, Louise, De, Parijat, Deshpande, Neeta, Durmaz, Erdem, Eickmeier, Frank, Elbarbary, Nancy Samir, Fillion, Marc, Jagadeesh, Sujatha M., Kershaw, Melanie, Khan, Waqas I., Mlynarski, Wojciech, Noyes, Kathryn, Peters, Catherine J., Shaw, Nick, Tiron, Irina, Turkkahraman, Doga, Turner, Lesley, Eltonbary, Khadiga Y., Yuksel, Bilgin
Publicado no Hum Mol Genet (2014)