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Page 1
An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.
Tzetis M, Stefanaki K, Syrmou A, Kosma K, Leze E, Giannikou K, Oikonomakis V, Sofocleous C, Choulakis M, Kolialexi A, Makrythanasis P, Kitsiou-Tzeli S. Tzetis M, et al. Among authors: makrythanasis p. Birth Defects Res A Clin Mol Teratol. 2012 Jul;94(7):561-6. doi: 10.1002/bdra.23038. Epub 2012 Jun 22. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22730277
Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis.
Tzetis M, Kaliakatsos M, Fotoulaki M, Papatheodorou A, Doudounakis S, Tsezou A, Makrythanasis P, Kanavakis E, Nousia-Arvanitakis S. Tzetis M, et al. Among authors: makrythanasis p. Clin Genet. 2007 May;71(5):451-7. doi: 10.1111/j.1399-0004.2007.00788.x. Clin Genet. 2007. PMID: 17489851
Development of a novel microarray methodology for the study of SNPs in the promoter region of the TNF-alpha gene: their association with obstructive pulmonary disease in Greek patients.
Papatheodorou A, Latsi P, Vrettou C, Dimakou A, Chroneou A, Makrythanasis P, Kaliakatsos M, Orfanidou D, Roussos C, Kanavakis E, Tzetis M. Papatheodorou A, et al. Among authors: makrythanasis p. Clin Biochem. 2007 Aug;40(12):843-50. doi: 10.1016/j.clinbiochem.2007.03.024. Epub 2007 Apr 19. Clin Biochem. 2007. PMID: 17509552
Development of novel microarray methodology for the study of mutations in the SERPINA1 and ADRB2 genes--their association with Obstructive Pulmonary Disease and Disseminated Bronchiectasis in Greek patients.
Papatheodorou A, Makrythanasis P, Kaliakatsos M, Dimakou A, Orfanidou D, Roussos C, Kanavakis E, Tzetis M. Papatheodorou A, et al. Among authors: makrythanasis p. Clin Biochem. 2010 Jan;43(1-2):43-50. doi: 10.1016/j.clinbiochem.2009.08.026. Epub 2009 Sep 10. Clin Biochem. 2010. PMID: 19747908
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. Genet Test Mol Biomarkers. 2010 Aug;14(4):577-84. doi: 10.1089/gtmb.2009.0198. Genet Test Mol Biomarkers. 2010. PMID: 20722470
Familial Pelizaeus-Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus.
Kitsiou-Tzeli S, Konstantinidou A, Sofocleous C, Kosma K, Syrmou A, Giannikou K, Sifakis S, Makrythanasis P, Tzetis M. Kitsiou-Tzeli S, et al. Among authors: makrythanasis p. Birth Defects Res A Clin Mol Teratol. 2012 Jun;94(6):494-8. doi: 10.1002/bdra.23015. Epub 2012 Apr 18. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22511562
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