The english version of the website is under development. Wherever text appears in Greek, it means it has not been translated yet.

Publications

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

Export 18 results:
Author Title Type [ Year(Asc)]
Filters: Author is Lambropoulos, Alexandros  [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.
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.
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.
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.
2018
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.
2017
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.
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.
2015
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.
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.
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.
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.
2013
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., 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.
2012
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.
2009
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.

Contact

Secretariat of the School of Medicine
 

Connect

School of Medicine's presence in social networks
Follow Us or Connect with us.