Δημοσιεύσεις

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

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Συντάκτης Τίτλος [ Τύπος(Desc)] Έτος
Φίλτρα: Συντάκτης is Lambropoulos, Alexandros  [Clear All Filters]
Journal Article
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.
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.
Anastasopoulos, E., Kakoulidou A., Coleman A. L., Sinsheimer J. S., M Wilson R., Yu F., et al. (2012).  Association of sequence variation in the CX3CR1 gene with geographic atrophy age-related macular degeneration in a Greek population.. Curr Eye Res. 37(12), 1148-55.
Patsatsi, A., Meltzanidou P., Katafigiotis S., Sotiriadis D., Schmidt E., & Lambropoulos A. (2017).  Chronic bullous disease of childhood with IgG reactivity to p200 antigen.. Int J Dermatol. 56(7), 773-775.
Patsatsi, A., Kyriakou A., Giannakou A., Pavlitou-Tsiontsi A., Lambropoulos A., & Sotiriadis D. (2014).  Clinical significance of anti-desmoglein-1 and -3 circulating autoantibodies in Pemphigus Patients Measured by Area Index and Intensity Score.. Acta Derm Venereol. 94(2), 203-6.
Aung, T., Ozaki M., Mizoguchi T., R Allingham R., Li Z., Haripriya A., et al. (2015).  A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.. Nat Genet. 47(4), 387-92.
Aung, T., Ozaki M., Mizoguchi T., R Allingham R., Li Z., Haripriya A., et al. (2015).  Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.. Nat Genet. 47(6), 689.
Meltzanidou, P., Patsatsi A., Kyriakou A., Vareli K., & Lambropoulos A. (2019).  Detection of IgG Autoantibodies against Desmocollin-3 in Greek Patients with Pemphigus.. Acta Dermatovenerol Croat. 27(1), 8-10.
Founti, P., Haidich A-B., Chatzikyriakidou A., Salonikiou A., Anastasopoulos E., Pappas T., et al. (2015).  Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-Analysis.. Ann Hum Genet. 79(6), 431-50.
Aung, T., Ozaki M., Lee M. Chin, Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., et al. (2017).  Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.. Nat Genet. 49(7), 993-1004.
Chatzikyriakidou, A., Voulgari P. V., Lambropoulos A., & Drosos A. A. (2013).  Genetics in rheumatoid arthritis beyond HLA genes: what meta-analyses have shown?. Semin Arthritis Rheum. 43(1), 29-38.
Chatzikyriakidou, A., Founti P., Melidou A., Minti F., Bouras E., Anastasopoulos E., et al. (2018).  MicroRNA-related polymorphisms in pseudoexfoliation syndrome, pseudoexfoliative glaucoma, and primary open-angle glaucoma.. Ophthalmic Genet. 39(5), 603-609.
Fountzilas, G., Kalogera-Fountzila A., Lambaki S., Wirtz R. M., Nikolaou A., Karayannopoulou G., et al. (2009).  MMP9 but Not EGFR, MET, ERCC1, P16, and P-53 Is Associated with Response to Concomitant Radiotherapy, Cetuximab, and Weekly Cisplatin in Patients with Locally Advanced Head and Neck Cancer.. J Oncol. 2009, 305908.
Patsatsi, A., Kyriakou A., Douma S., Kokolios M., Meltzanidou P., Lambropoulos A., et al. (2019).  Nichtendemischer erythrodermischer Pemphigus foliaceus: Ein Fall mit verzögerter Diagnose und Response auf Rituximab.. J Dtsch Dermatol Ges. 17(5), 537-539.
Patsatsi, A., Kyriakou A., Douma S., Kokolios M., Meltzanidou P., Lambropoulos A., et al. (2019).  Non-endemic erythrodermic pemphigus foliaceus: a case with delayed diagnosis and response to rituximab.. J Dtsch Dermatol Ges. 17(5), 537-539.
Demirtzoglou, G., Chrysoglou S-I., Katopodi T., Dimitroulas T., Iakovidou-Kritsi Z., Garyfallos A., et al. (2023).  Olanzapine's Cytogenetic Effect on T Lymphocytes in Systemic Lupus Erythematosus and Rheumatoid Arthritis Patients: In Vitro Study.. Cureus. 15(4), e37683.
Berner, D., Hoja U., Zenkel M., Ross J. Julian, Uebe S., Paoli D., et al. (2019).  The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.. Hum Mol Genet. 28(15), 2531-2548.
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.
Chatzikyriakidou, A., Voulgari P. V., Lambropoulos A., Georgiou I., & Drosos A. A. (2013).  Validation of the TAGAP rs212389 polymorphism in rheumatoid arthritis susceptibility.. Joint Bone Spine. 80(5), 543-4.

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