Polat S - Search Results

1

Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.

Menabò S, Polat S, Baldazzi L, Kulle AE, Holterhus PM, Grötzinger J, Fanelli F, Balsamo A, Riepe FG. Menabò S, et al. Among authors: polat s. Eur J Hum Genet. 2020 May;28(5):692. doi: 10.1038/s41431-020-0587-y. Eur J Hum Genet. 2020. PMID: 32071409 Free PMC article.

2

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.

Menabò S, Polat S, Baldazzi L, Kulle AE, Holterhus PM, Grötzinger J, Fanelli F, Balsamo A, Riepe FG. Menabò S, et al. Among authors: polat s. Eur J Hum Genet. 2014 May;22(5):610-6. doi: 10.1038/ejhg.2013.197. Epub 2013 Sep 11. Eur J Hum Genet. 2014. PMID: 24022297 Free PMC article.

3

Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency.

Polat S, Kulle A, Karaca Z, Akkurt I, Kurtoglu S, Kelestimur F, Grötzinger J, Holterhus PM, Riepe FG. Polat S, et al. Eur J Endocrinol. 2014 Apr 10;170(5):697-706. doi: 10.1530/EJE-13-0737. Print 2014 May. Eur J Endocrinol. 2014. PMID: 24536089

4

The role of androgen receptor CAG repeat polymorphism in androgen excess disorder and idiopathic hirsutism.

Polat S, Karaburgu S, Unluhizarci K, Dündar M, Özkul Y, Arslan YK, Karaca Z, Kelestimur F. Polat S, et al. J Endocrinol Invest. 2020 Sep;43(9):1271-1281. doi: 10.1007/s40618-020-01215-7. Epub 2020 Mar 12. J Endocrinol Invest. 2020. PMID: 32166698

5

A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients.

Dundar M, Kiraz A, Emirogullari EF, Saatci CE, Taheri S, Baskol M, Polat S, Ozkul Y. Dundar M, et al. Among authors: polat s. Ann Saudi Med. 2012 Jul-Aug;32(4):343-8. doi: 10.5144/0256-4947.2012.343. Ann Saudi Med. 2012. PMID: 22705602 Free PMC article.

6

Comprehensive genotyping of Turkish women with hirsutism.

Polat S, Karaburgu S, Ünlühizarcı K, Dündar M, Özkul Y, Arslan YK, Karaca Z, Kelestimur F. Polat S, et al. J Endocrinol Invest. 2019 Sep;42(9):1077-1087. doi: 10.1007/s40618-019-01028-3. Epub 2019 Feb 27. J Endocrinol Invest. 2019. PMID: 30811025

7

17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in CYP21A2 Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analyses.

Polat S, Arslan YK. Polat S, et al. J Clin Res Pediatr Endocrinol. 2022 Mar 3;14(1):56-68. doi: 10.4274/jcrpe.galenos.2021.2021.0184. Epub 2021 Nov 8. J Clin Res Pediatr Endocrinol. 2022. PMID: 34743977 Free PMC article.

8

Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene.

Güven A, Polat S. Güven A, et al. Among authors: polat s. J Clin Res Pediatr Endocrinol. 2017 Mar 1;9(1):85-90. doi: 10.4274/jcrpe.3306. Epub 2016 Jul 29. J Clin Res Pediatr Endocrinol. 2017. PMID: 27476613 Free PMC article.

9

Five variants of the superoxide dismutase genes in Turkish women with polycystic ovary syndrome.

Polat S, Şimşek Y. Polat S, et al. Free Radic Res. 2020 Jun;54(6):467-476. doi: 10.1080/10715762.2020.1802022. Epub 2020 Aug 5. Free Radic Res. 2020. PMID: 32715851

10

Vitamin E and Selenium Reduce Prednisolone Side Effects in Rat Hearts.

Bardas E, Arslan YK, Polat S, Erisir M, Uslu GA, Cetin N, Cicek B. Bardas E, et al. Among authors: polat s. Int J Vitam Nutr Res. 2020 Jun;90(3-4):309-317. doi: 10.1024/0300-9831/a000582. Epub 2019 Apr 16. Int J Vitam Nutr Res. 2020. PMID: 30987549

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