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Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions.
Baran RT, Sürer-Adanır A, Karakurt MN, Dündar M, Aydın M, Özbek MN, Demirbilek H. Baran RT, et al. Among authors: demirbilek h. Turk J Pediatr. 2018;60(5):554-561. doi: 10.24953/turkjped.2018.05.013. Turk J Pediatr. 2018. PMID: 30968638 Free article.
Baran RT, Surer-Adanir A, Karakurt MN, Dundar M, Aydin M, Ozbek MN, Demirbilek H. Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions. ...
Baran RT, Surer-Adanir A, Karakurt MN, Dundar M, Aydin M, Ozbek MN, Demirbilek H. Evaluation of psychological characteristics …
Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism.
Gürbüz F, Kotan LD, Mengen E, Şıklar Z, Berberoğlu M, Dökmetaş S, Kılıçlı MF, Güven A, Kirel B, Saka N, Poyrazoğlu Ş, Cesur Y, Doğan M, Özen S, Özbek MN, Demirbilek H, Kekil MB, Temiz F, Önenli Mungan N, Yüksel B, Topaloğlu AK. Gürbüz F, et al. Among authors: demirbilek h. J Clin Res Pediatr Endocrinol. 2012 Sep;4(3):121-6. doi: 10.4274/jcrpe.725. Epub 2012 Jul 5. J Clin Res Pediatr Endocrinol. 2012. PMID: 22766261 Free PMC article.
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.
Demirbilek H, Arya VB, Ozbek MN, Akinci A, Dogan M, Demirel F, Houghton J, Kaba S, Guzel F, Baran RT, Unal S, Tekkes S, Flanagan SE, Ellard S, Hussain K. Demirbilek H, et al. Eur J Endocrinol. 2014 Jun;170(6):885-92. doi: 10.1530/EJE-14-0045. Epub 2014 Mar 31. Eur J Endocrinol. 2014. PMID: 24686051
Prepubertal unilateral gynecomastia: report of 2 cases.
Demirbilek H, Bacak G, Baran RT, Avcı Y, Baran A, Keleş A, Özbek MN, Alanay Y, Hussain K. Demirbilek H, et al. J Clin Res Pediatr Endocrinol. 2014 Dec;6(4):250-3. doi: 10.4274/Jcrpe.1477. J Clin Res Pediatr Endocrinol. 2014. PMID: 25541897 Free PMC article.
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.
Demirbilek H, Arya VB, Ozbek MN, Houghton JA, Baran RT, Akar M, Tekes S, Tuzun H, Mackay DJ, Flanagan SE, Hattersley AT, Ellard S, Hussain K. Demirbilek H, et al. Eur J Endocrinol. 2015 Jun;172(6):697-705. doi: 10.1530/EJE-14-0852. Epub 2015 Mar 9. Eur J Endocrinol. 2015. PMID: 25755231 Free PMC article.
77 results