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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

Export 73 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Polymorphism, Genetic  [Clear All Filters]
2019
Chatzikyriakidou, A., Kyriakou A., Meltzanidou P., Lambropoulos A., & Patsatsi A. (2019).  Association of NFKB1 -94ATTG ins/del polymorphism (rs28362491) with pemphigus vulgaris.. Exp Dermatol. 28(8), 972-975.
Bouziana, S., Tziomalos K., Goulas A., Vyzantiadis T-A., Papadopoulou M., Panderi A., et al. (2019).  Effects of major adipokines and the -420 C > G resistin gene polymorphism on the long-term outcome of patients with acute ischemic stroke.. Int J Neurosci. 129(10), 978-985.
Dardiotis, E., Aloizou A-M., Siokas V., Tsouris Z., Rikos D., Marogianni C., et al. (2019).  Paraoxonase-1 genetic polymorphisms in organophosphate metabolism.. Toxicology. 411, 24-31.
Karananou, P., Tramma D., Katafigiotis S., Alataki A., Lambropoulos A., & Papadopoulou-Alataki E. (2019).  The Role of TLR4 Asp299Gly and TLR4 Thr399Ile Polymorphisms in the Pathogenesis of Urinary Tract Infections: First Evaluation in Infants and Children of Greek Origin.. J Immunol Res. 2019, 6503832.
Rikos, D., Siokas V., Aloizou A-M., Tsouris Z., Aslanidou P., Koutsis G., et al. (2019).  TREM2 R47H (rs75932628) variant is unlikely to contribute to Multiple Sclerosis susceptibility and severity in a large Greek MS cohort.. Mult Scler Relat Disord. 35, 116-118.
2018
Agapakis, D., Panderi A., Gbandi E., Savopoulos C., Kouvelas D., Hatzitolios A. Ioannis, et al. (2018).  The ABCB1 2677G>T/A polymorphism is associated with baseline blood HDL-cholesterol levels in newly diagnosed hyperlipidemic patients.. Hellenic J Cardiol. 59(2), 122-126.
Roumeliotis, A. K., Roumeliotis S. K., Panagoutsos S. A., Tsetsos F., Georgitsi M., Manolopoulos V., et al. (2018).  Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy.. Int Urol Nephrol. 50(2), 321-329.
Bouziana, S. D., Tziomalos K., Goulas A., Vyzantiadis T-A., Panderi A., & Ηatzitolios A. Ι. (2018).  Major Adipokines and the -420C>G Resistin Gene Polymorphism as Predictors of Acute Ischemic Stroke Severity and In-Hospital Outcome.. J Stroke Cerebrovasc Dis. 27(4), 963-970.
Tsolaki, A. C., Gatzima O., Daniilidou M., Lazarou E., Bamidis P. D., Verykouki E., et al. (2018).  Prevalence of Apolipoprotein E Polymorphisms in Alzheimer's Disease, Mild Cognitive Impairment, and Healthy Elderly: A Northern Greece Study.. Neurodegener Dis. 18(4), 216-224.
2017
Karalexi, M. A., Dessypris N., Thomopoulos T. P., Ntouvelis E., Kantzanou M., Diamantaras A-A., et al. (2017).  Parental alcohol consumption and risk of leukemia in the offspring: a systematic review and meta-analysis.. Eur J Cancer Prev. 26(5), 433-441.
Chatzidimitriou, M., Chatzidimitriou D., Mavridou M., Anetakis C., Chatzopoulou F., Lialiaris T., et al. (2017).  Thrombophilic gene polymorphisms and recurrent pregnancy loss in Greek women.. Int J Lab Hematol. 39(6), 590-595.
2016
Goulielmos, G. N., Chiaroni-Clarke R. C., Dimopoulou D. G., Zervou M. I., Trachana M., Pratsidou-Gertsi P., et al. (2016).  Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population.. Pediatr Rheumatol Online J. 14(1), 25.
Agapakis, D., Savopoulos C., Kypreos K. E., Gbandi E., Iliadis S., Hatzitolios A. I., et al. (2016).  Association of the CETP Taq1B and LIPG Thr111Ile Polymorphisms with Glycated Hemoglobin and Blood Lipids in Newly Diagnosed Hyperlipidemic Patients.. Can J Diabetes. 40(6), 515-520.
Gbandi, E., Goulas A., Sevastianos V., Hadziyannis S., Panderi A., Koskinas J., et al. (2016).  Common ABCB1 polymorphisms in Greek patients with chronic hepatitis C infection: A comparison with hyperlipidemic patients and the general population.. Pharmacol Rep. 68(2), 476-82.
Kyriakidis, I., & Papaioannidou P. (2016).  Estrogen receptor beta and ovarian cancer: a key to pathogenesis and response to therapy.. Arch Gynecol Obstet. 293(6), 1161-8.
Yavropoulou, M. P., Kollia P., Chatzidimitriou D., Samara S., Skoura L., & Yovos J. G. (2016).  Severe osteoporosis with multiple spontaneous vertebral fractures in a young male carrying triple polymorphisms in the vitamin D receptor, collagen type 1, and low-density lipoprotein receptor-related peptide 5 genes.. Hormones (Athens). 15(4), 551-556.
2015
Chatzikyriakidou, A., Aidinidou L., Giannopoulos A., Papadopoulou-Legbelou K., Kalinderi K., & Fidani L. (2015).  Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients.. Cardiol Young. 25(4), 681-3.
Kotanidou, E. P., Kalinderi K., Kyrgios I., Efraimidou S., Fidani L., Papadopoulou-Alataki E., et al. (2015).  Apelin and G212A apelin receptor gene polymorphism in obese and diabese youth.. Pediatr Obes. 10(3), 213-9.
2014
Anastasopoulos, E., Coleman A. L., M Wilson R., Sinsheimer J. S., Yu F., Katafigiotis S., et al. (2014).  Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study.. Invest Ophthalmol Vis Sci. 55(7), 4238-43.
Vasiliadis, I., Kolovou G., Kolovou V., Giannakopoulou V., Boutsikou M., Katsiki N., et al. (2014).  Gene polymorphisms and thyroid function in patients with heart failure.. Endocrine. 45(1), 46-54.
Konstantopoulou, I., Tsitlaidou M., Fostira F., Pertesi M., Stavropoulou A-V., Triantafyllidou O., et al. (2014).  High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.. Clin Genet. 85(1), 36-42.
Pana, Z-D., Farmaki E., & Roilides E. (2014).  Host genetics and opportunistic fungal infections.. Clin Microbiol Infect. 20(12), 1254-64.
Chatzikyriakidou, A., Voulgari P. V., & Drosos A. A. (2014).  Lack of association of the autophagy-related gene polymorphism ATG16L1 rs2241880 in RA predisposition.. Rheumatol Int. 34(4), 477-9.
Chatzikyriakidou, A., Voulgari P. V., & Drosos A. A. (2014).  Lack of association of the GSDMB gene at locus 17q12 with predisposition to rheumatoid arthritis.. Clin Exp Rheumatol. 32(3), 447.
Pana, Z. Dorothea, Samarah F., Papi R., Antachopoulos C., Papageorgiou T., Farmaki E., et al. (2014).  Mannose binding lectin and ficolin-2 polymorphisms are associated with increased risk for bacterial infections in children with B acute lymphoblastic leukemia.. Pediatr Blood Cancer. 61(6), 1017-22.

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