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Hyperinsulinaemic hypoglycaemia in children and adults.
Shah P, Rahman SA, Demirbilek H, Güemes M, Hussain K. Shah P, et al. Among authors: demirbilek h. Lancet Diabetes Endocrinol. 2017 Sep;5(9):729-742. doi: 10.1016/S2213-8587(16)30323-0. Epub 2016 Dec 1. Lancet Diabetes Endocrinol. 2017. PMID: 27915035 Review.
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
Persistent hyperinsulinaemic hypoglycaemia in infancy.
Shah P, Demirbilek H, Hussain K. Shah P, et al. Among authors: demirbilek h. Semin Pediatr Surg. 2014 Apr;23(2):76-82. doi: 10.1053/j.sempedsurg.2014.03.005. Epub 2014 Mar 15. Semin Pediatr Surg. 2014. PMID: 24931352 Review.
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.
83 results