Kostoulas C - Search Results

1

Biological and Clinical Significance of Mosaicism in Human Preimplantation Embryos.

Bouba I, Hatzi E, Ladias P, Sakaloglou P, Kostoulas C, Georgiou I. Bouba I, et al. Among authors: kostoulas c. J Dev Biol. 2021 May 7;9(2):18. doi: 10.3390/jdb9020018. J Dev Biol. 2021. PMID: 34066950 Free PMC article. Review.

2

Gender association of the angiotensin-converting enzyme gene with ischaemic stroke.

Markoula S, Giannopoulos S, Kostoulas C, Tatsioni A, Bouba I, Maranis S, Georgiou I, Kyritsis AP. Markoula S, et al. Among authors: kostoulas c. J Renin Angiotensin Aldosterone Syst. 2011 Dec;12(4):510-5. doi: 10.1177/1470320310391333. Epub 2011 Mar 18. J Renin Angiotensin Aldosterone Syst. 2011. PMID: 21421656 Free article.

3

Renin-angiotensin-aldosterone system genes and nonarteritic anterior ischemic optic neuropathy.

Markoula S, Giannopoulos S, Asproudis I, Kostoulas C, Nikas A, Bagli E, Kyritsis AP, Georgiou I. Markoula S, et al. Among authors: kostoulas c. Mol Vis. 2011;17:1254-60. Epub 2011 May 6. Mol Vis. 2011. PMID: 21633717 Free PMC article.

4

Retrotransposon expression and incorporation of cloned human and mouse retroelements in human spermatozoa.

Lazaros L, Kitsou C, Kostoulas C, Bellou S, Hatzi E, Ladias P, Stefos T, Markoula S, Galani V, Vartholomatos G, Tzavaras T, Georgiou I. Lazaros L, et al. Among authors: kostoulas c. Fertil Steril. 2017 Mar;107(3):821-830. doi: 10.1016/j.fertnstert.2016.12.027. Epub 2017 Jan 27. Fertil Steril. 2017. PMID: 28139237 Free article.

5

ATG16L1 T300A polymorphism is associated with Crohn's disease in a Northwest Greek cohort, but ECM1 T130M and G290S polymorphisms are not associated with ulcerative colitis.

Tsianos VE, Kostoulas C, Gazouli M, Frillingos S, Georgiou I, Christodoulou DK, Katsanos KH, Tsianos EV. Tsianos VE, et al. Among authors: kostoulas c. Ann Gastroenterol. 2020 Jan-Feb;33(1):38-44. doi: 10.20524/aog.2019.0434. Epub 2019 Nov 21. Ann Gastroenterol. 2020. PMID: 31892796 Free PMC article.

6

A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.

Efstathiadou ZA, Kostoulas C, Polyzos SA, Adamidou F, Georgiou I, Kita M. Efstathiadou ZA, et al. Among authors: kostoulas c. Endocrine. 2021 Jan;71(1):208-215. doi: 10.1007/s12020-020-02446-7. Epub 2020 Aug 9. Endocrine. 2021. PMID: 32772338

7

Correction to: A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.

Efstathiadou ZA, Kostoulas C, Polyzos SA, Adamidou F, Georgiou I, Kita M. Efstathiadou ZA, et al. Among authors: kostoulas c. Endocrine. 2020 Dec;70(3):659-660. doi: 10.1007/s12020-020-02479-y. Endocrine. 2020. PMID: 33025564

8

An open study of valproate in subfertile men with epilepsy.

Markoula S, Siarava E, Kostoulas C, Zikopoulos A, Georgiou I. Markoula S, et al. Among authors: kostoulas c. Acta Neurol Scand. 2020 Oct;142(4):317-322. doi: 10.1111/ane.13311. Epub 2020 Jul 20. Acta Neurol Scand. 2020. PMID: 33378111

9

Development and Validation of a Targeted 'Liquid' NGS Panel for Treatment Customization in Patients with Metastatic Colorectal Cancer.

Kastrisiou M, Zarkavelis G, Kougioumtzi A, Sakaloglou P, Kostoulas C, Georgiou I, Batistatou A, Pentheroudakis G, Magklara A. Kastrisiou M, et al. Among authors: kostoulas c. Diagnostics (Basel). 2021 Dec 16;11(12):2375. doi: 10.3390/diagnostics11122375. Diagnostics (Basel). 2021. PMID: 34943612 Free PMC article.

10

Unusual N Gene Dropout and Ct Value Shift in Commercial Multiplex PCR Assays Caused by Mutated SARS-CoV-2 Strain.

Bozidis P, Tsaousi ET, Kostoulas C, Sakaloglou P, Gouni A, Koumpouli D, Sakkas H, Georgiou I, Gartzonika K. Bozidis P, et al. Among authors: kostoulas c. Diagnostics (Basel). 2022 Apr 13;12(4):973. doi: 10.3390/diagnostics12040973. Diagnostics (Basel). 2022. PMID: 35454022 Free PMC article.

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