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Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell.
Oçal G, Flanagan SE, Hacihamdioğlu B, Berberoğlu M, Siklar Z, Ellard S, Savas Erdeve S, Okulu E, Akin IM, Atasay B, Arsan S, Yağmurlu A. Oçal G, et al. Among authors: siklar z. J Pediatr Endocrinol Metab. 2011;24(11-12):1019-23. doi: 10.1515/jpem.2011.347. J Pediatr Endocrinol Metab. 2011. PMID: 22308858
Syndromic disorders with short stature.
Şıklar Z, Berberoğlu M. Şıklar Z, et al. J Clin Res Pediatr Endocrinol. 2014;6(1):1-8. doi: 10.4274/Jcrpe.1149. J Clin Res Pediatr Endocrinol. 2014. PMID: 24637303 Free PMC article. Review.
Childhood Sustained Hypercalcemia: A Diagnostic Challenge.
Çullas İlarslan NE, Şıklar Z, Berberoğlu M. Çullas İlarslan NE, et al. Among authors: siklar z. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):315-322. doi: 10.4274/jcrpe.4247. Epub 2017 Apr 26. J Clin Res Pediatr Endocrinol. 2017. PMID: 28443817 Free PMC article.
164 results