Poulou M - Search Results

1

Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients.

Makrythanasis P, Tzetis M, Rapti A, Papatheodorou A, Tsipi M, Kitsiou S, Tsiamouri A, Poulou M, Roussos C, Kanavakis E. Makrythanasis P, et al. Among authors: poulou m. Genet Test Mol Biomarkers. 2010 Aug;14(4):577-84. doi: 10.1089/gtmb.2009.0198. Genet Test Mol Biomarkers. 2010. PMID: 20722470

2

Association of the CALM1 core promoter polymorphism with knee osteoarthritis in patients of Greek origin.

Poulou M, Kaliakatsos M, Tsezou A, Kanavakis E, Malizos KN, Tzetis M. Poulou M, et al. Genet Test. 2008 Jun;12(2):263-5. doi: 10.1089/gte.2007.0114. Genet Test. 2008. PMID: 18452398

3

Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene.

Poulou M, Fylaktou I, Fotoulaki M, Kanavakis E, Tzetis M. Poulou M, et al. J Cyst Fibros. 2012 Jul;11(4):344-8. doi: 10.1016/j.jcf.2012.01.004. Epub 2012 Feb 11. J Cyst Fibros. 2012. PMID: 22326559 Free article.

4

Genotyping efficiency of 2 primer sets and an unlabeled oligonucleotide probe for the p.Phe508del in exon 10 of the CFTR gene as determined with high-resolution melting analysis.

Poulou M, Destouni A, Fylaktou I, Kanavakis E, Tzetis M. Poulou M, et al. Clin Chem. 2012 Oct;58(10):1490-2. doi: 10.1373/clinchem.2012.189696. Epub 2012 Aug 15. Clin Chem. 2012. PMID: 22896710 No abstract available.

5

Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR.

Poulou M, Destouni A, Kakourou G, Kanavakis E, Tzetis M. Poulou M, et al. J Cyst Fibros. 2014 Dec;13(6):617-22. doi: 10.1016/j.jcf.2014.04.002. Epub 2014 Apr 29. J Cyst Fibros. 2014. PMID: 24784896 Free article.

6

Are ALOX5AP gene SNPs a risk or protective factor for stroke?

Papapostolou A, Spengos K, Fylaktou I, Poulou M, Gountas I, Kitsiou-Tzeli S, Kanavakis E, Tzetis M. Papapostolou A, et al. Among authors: poulou m. Gene. 2014 Sep 10;548(1):56-60. doi: 10.1016/j.gene.2014.07.007. Epub 2014 Jul 8. Gene. 2014. PMID: 25010723

7

BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients.

Delaveri A, Rapti A, Poulou M, Fylaktou E, Tsipi M, Roussos C, Makrythanasis P, Kanavakis E, Tzetis M. Delaveri A, et al. Among authors: poulou m. Meta Gene. 2014 Aug 31;2:619-30. doi: 10.1016/j.mgene.2014.07.009. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606445 Free PMC article.

8

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).

Destouni A, Poulou M, Kakourou G, Vrettou C, Tzetis M, Traeger-Synodinos J, Kitsiou-Tzeli S. Destouni A, et al. Among authors: poulou m. J Cyst Fibros. 2016 Mar;15(2):163-70. doi: 10.1016/j.jcf.2015.09.009. Epub 2015 Oct 19. J Cyst Fibros. 2016. PMID: 26493493 Free article.

9

Multi-allele genotyping platform for the simultaneous detection of mutations in the Wilson disease related ATP7B gene.

Amvrosiadou M, Petropoulou M, Poulou M, Tzetis M, Kanavakis E, Christopoulos TK, Ioannou PC. Amvrosiadou M, et al. Among authors: poulou m. J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Dec 1;1006:201-208. doi: 10.1016/j.jchromb.2015.10.036. Epub 2015 Oct 30. J Chromatogr B Analyt Technol Biomed Life Sci. 2015. PMID: 26580967

10

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases.

Tsipi M, Tzetis M, Kosma K, Moschos M, Braoudaki M, Poulou M, Kanavakis E, Kitsiou-Tzeli S. Tsipi M, et al. Among authors: poulou m. Meta Gene. 2016 Feb 16;8:37-43. doi: 10.1016/j.mgene.2016.02.002. eCollection 2016 Jun. Meta Gene. 2016. PMID: 27014590 Free PMC article.

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