Browsing by Author "Akcay, Teoman"
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Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study
Hatun, S.; Mutlu, G. Yesiltepe; Cinaz, P.; Turan, S.; Ekberzade, A.; Bereket, A.; Erbas, M. Y.; Akcay, Teoman; Onal, H.; Bolu, S.; Arslanoglu, I.; Doger, E.; Yilmaz, A. A.; Ucakturk, A.; Karabulut, G. S.; Tuhan, H. U.; Demir, K.; Erdeve, S. S.; Aycan, Z.; Nalbantoglu, O.; Kara, C.; Gungor, N.; Darendeliler, Feyza; Bundak, Ruveyde; Anik, Ahmet; Ucar, Ahmet; Cayir, Atilla; Ergur, Ayca Torel; Ozcabi, Bahar; Haliloglu, Belma; Ozkan, Behzat; Eklioglu, Beray Selver; Kirel, Birgul; Bezen, Digdem; Vuralli, Dogus; Unal, Edip); Sagsak, Elif; Bugrul, Fuat; Catli, Gonul; Korkmaz, Huseyin Anil; Ozbek, Mehmet Nuri; Tayfun, Meltem; Genens, Mikayir; Buyuk, Muammer; Hatipoglu, Nihal; Abali, Saygin; Kiremitci, Seniha; Curek, Yusuf; Siklar, Zeynep (Wiley, 2019)Aims To describe the baseline clinical and laboratory findings and treatment modalities of 367 children and adolescents diagnosed with Type 2 diabetes in various paediatric endocrinology centres in Turkey. Methods A standard ... -
Comprehensive genetic testing shows one in five children with diabetes and non-autoimmune extra-pancreatic features have monogenic aetiology
Patel, Kashyap A.; Colclough, Kevin; Ozbek, Mehmet Nuri; Yildiz, Melek; Guran, Tulay; Kocyigit, Cemil; Acar, Sezer; Siklar, Zeynep; Atar, Muge; Johnson, Matt B.; Flanagan, Sarah E.; Ellard, Sian; Cizmecioglu, Filiz Mine; Berberoglu, Merih; Demir, Korcan; Catli, Gonul; Bas, Serpil; Akcay, Teoman; Demirbilek, Huseyin; Weedon, Michael N.; Hattersley, Andrew T. (Karger, 2018)Young onset Diabetes with non-autoimmune extra pancreatic features -
Distribution of α-actinin-3 rs1815739 and angiotensin-1 converting enzyme indel polymorphisms in Turkish bodybuilders
Polat, Tolga; Dogan, Canan Sercan; Dogan, Murat; Akcay, Teoman; Ulucan, Korkut (Spandidos Publications, 2020)The determination of the genetic profiles of successful athletes and the effects of these genetic parameters on athletic performance is gaining increasing interest. The majority of studies assessing the genetics of athletes ... -
Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism
Weger, Meltem; Weger, Benjamin D.; Goerling, Benjamin; Poschet, Gernot; Yildiz, Melek; Hell, Ruediger; Luy, Burkhard; Akcay, Teoman; Guran, Tulay; Dickmeis, Thomas; Mueller, Ferenc; Krone, Nils (Elsevier, 2018)Background: Deficient glucocorticoid biosynthesis leading to adrenal insufficiency is life-threatening and is associated with significant co-morbidities. The affected pathways underlying the pathophysiology of co-morbidities ... -
Multivitamin with L-Arginine supplementation can increase linear growth velocity in children with idiopathic short stature without affecting bone maturation
Akcagil, Omer; Ulucan, Korkut; Akcay, Teoman (MATTIOLI 1885, 2020)L-arginine is a well-known growth hormone (GH) stimulator. The aim of the present study was to investigate the effect of L-arginine supplementation on growth velocity in prepubertal boys with idiopathic short stature. In ... -
Retrospective analysis of cases with premature thelarche
Kihtir, Hasan Serdar; Akcay, Teoman (2020)Objective: Premature thelarche is defined as breast enlargement in females (younger than eight years) without other signs of secondary gender character development. Although it is common in the first two years of life, ... -
Revisiting Classical 3 beta-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases
Guran, Tulay; Kara, Cengiz; Yildiz, Melek; Bitkin, Eda C.; Haklar, Goncagul; Lin, Jen-Chieh; Keskin, Mehmet; Barnard, Lise; Anik, Ahmet; Catli, Gonul; Guven, Ayla; Kirel, Birgul; Tutunculer, Filiz; Onal, Hasan; Turan, Serap; Akcay, Teoman; Atay, Zeynep; Yilmaz, Gulay C.; Mamadova, Jamala; Akbarzade, Azad; Sirikci, Onder; Storbeck, Karl-Heinz; Baris, Tugba; Chung, Bon-Chu; Bereket, Abdullah (Endocrine Soc, 2020)Context: The clinical effects of classical 3 beta-hydroxysteroid dehydrogenase 2 (3 beta HSD2) deficiency are insufficiently defined due to a limited number of published cases. Objective: To evaluate an integrated steroid ... -
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics
Patel, Kashyap A.; Ozbek, Mehmet N.; Yildiz, Melek; Guran, Tulay; Kocyigit, Cemil; Acar, Sezer; Siklar, Zeynep; Akcay, Teoman (SPRINGER, 2021)Aims/hypothesis Current clinical guidelines for childhood-onset monogenic diabetes outside infancy are mainly focused on identifying and testing for dominantly inherited, predominantly MODY genes. There are no systematic ...
