Publications by authors named "Seher Polat"

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Association between (rs4343 and rs1799752), (rs5186), and (rs2227631) polymorphisms in the host and the severity of Covid-19 infection.
Seher Polat, Zühal Özer Şimşek

Nucleosides Nucleotides Nucleic Acids· December 2024

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Transgenerational impact of topical steroid application on superoxide dismutase activities of hypothalamus-pituitary-adrenal axis in rats.
Seher Polat, Armağan Caner

Can J Physiol Pharmacol· May 2022

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17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analyses.
Seher Polat, Yusuf Kemal Arslan

J Clin Res Pediatr Endocrinol· March 2022

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Vitamin E and Selenium Reduce Prednisolone Side Effects in Rat Hearts.
Ebru Bardas, Yusuf Kemal Arslan, Seher Polat, Mine Erisir, Gözde Atila Uslu

Int J Vitam Nutr Res· June 2020

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Five variants of the superoxide dismutase genes in Turkish women with polycystic ovary syndrome.
Seher Polat, Yasin Şimşek

Free Radic Res· June 2020

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Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.
Soara Menabò, Seher Polat, Lilia Baldazzi, Alexandra E Kulle, Paul-Martin Holterhus

Eur J Hum Genet· May 2020

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The possible protective effects of vitamin E and selenium administration in oxidative stress caused by high doses of glucocorticoid administration in the brain of rats.
Ebru Beytut, Seval Yilmaz, Mesut Aksakal, Seher Polat

J Trace Elem Med Biol· January 2018

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

J Clin Res Pediatr Endocrinol· March 2017

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Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.
Soara Menabò, Seher Polat, Lilia Baldazzi, Alexandra E Kulle, Paul-Martin Holterhus

Eur J Hum Genet· May 2014

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Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency.
Seher Polat, Alexandra Kulle, Züleyha Karaca, Ilker Akkurt, Selim Kurtoglu

Eur J Endocrinol· May 2014

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A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients.
Munis Dundar, Aslihan Kiraz, Elif Funda Emirogullari, Ccedil Etin Saatci, Serpil Taheri, Seher Polat

Ann Saudi Med· November 2012

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