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Page 1
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation.
Flanagan SE, Xie W, Caswell R, Damhuis A, Vianey-Saban C, Akcay T, Darendeliler F, Bas F, Guven A, Siklar Z, Ocal G, Berberoglu M, Murphy N, O'Sullivan M, Green A, Clayton PE, Banerjee I, Clayton PT, Hussain K, Weedon MN, Ellard S. Flanagan SE, et al. Among authors: bas f. Am J Hum Genet. 2013 Jan 10;92(1):131-6. doi: 10.1016/j.ajhg.2012.11.017. Epub 2012 Dec 27. Am J Hum Genet. 2013. PMID: 23273570 Free PMC article.
Hyperinsulinism in infancy--genetic aspects.
Darendeliler F, Bas F. Darendeliler F, et al. Among authors: bas f. Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:521-6. Pediatr Endocrinol Rev. 2006. PMID: 17551476 Review.
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study.
Baş F, Darendeliler F, Aycan Z, Çetinkaya E, Berberoğlu M, Sıklar Z, Öcal G, Timirci Ö, Çetinkaya S, Darcan Ş, Gökşen Şimşek D, Bideci A, Cinaz P, Böber E, Demir K, Bereket A, Turan S, Atabek ME, Tütüncüler F, Isbir T, Bozkurt N, Kabataş Eryılmaz S, Uzunhan O, Küçükemre Aydın B, Bundak R. Baş F, et al. Horm Res Paediatr. 2012;77(2):85-93. doi: 10.1159/000335172. Epub 2012 Mar 23. Horm Res Paediatr. 2012. PMID: 22456308
Adherence to growth hormone therapy: results of a multicenter study.
Aydın BK, Aycan Z, Sıklar Z, Berberoğlu M, Ocal G, Cetinkaya S, Baş VN, Kendirci HN, Cetinkaya E, Darcan S, Gökşen D, Evliyaoğlu O, Sükür M, Baş F, Darendeliler F. Aydın BK, et al. Among authors: bas vn, bas f. Endocr Pract. 2014 Jan;20(1):46-51. doi: 10.4158/EP13194.OR. Endocr Pract. 2014. PMID: 24013997
Metabolic syndrome in young people.
Poyrazoglu S, Bas F, Darendeliler F. Poyrazoglu S, et al. Among authors: bas f. Curr Opin Endocrinol Diabetes Obes. 2014 Feb;21(1):56-63. doi: 10.1097/01.med.0000436414.90240.2c. Curr Opin Endocrinol Diabetes Obes. 2014. PMID: 24247648 Review.
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
Baş F, Uyguner ZO, Darendeliler F, Aycan Z, Çetinkaya E, Berberoğlu M, Şiklar Z, Öcal G, Darcan Ş, Gökşen D, Topaloğlu AK, Yüksel B, Özbek MN, Ercan O, Evliyaoğlu O, Çetinkaya S, Şen Y, Atabek E, Toksoy G, Aydin BK, Bundak R. Baş F, et al. Endocrine. 2015 Jun;49(2):479-91. doi: 10.1007/s12020-014-0498-1. Epub 2014 Dec 11. Endocrine. 2015. PMID: 25500790
202 results