Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Συντάκτης [ Τίτλος] Τύπος Έτος Φίλτρα: Συντάκτης is Lambropoulos, Alexandros [Clear All Filters]
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.
(2014). Association of NFKB1 -94ATTG ins/del polymorphism (rs28362491) with pemphigus vulgaris..
Exp Dermatol. 28(8), 972-975.
(2019).
(2012). Chronic bullous disease of childhood with IgG reactivity to p200 antigen..
Int J Dermatol. 56(7), 773-775.
(2017). 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.
(2014). A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome..
Nat Genet. 47(4), 387-92.
(2015).
(2015). Detection of IgG Autoantibodies against Desmocollin-3 in Greek Patients with Pemphigus..
Acta Dermatovenerol Croat. 27(1), 8-10.
(2019).
(2015).
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci..
Nat Genet. 49(7), 993-1004.
(2017). Genetics in rheumatoid arthritis beyond HLA genes: what meta-analyses have shown?.
Semin Arthritis Rheum. 43(1), 29-38.
(2013). MicroRNA-related polymorphisms in pseudoexfoliation syndrome, pseudoexfoliative glaucoma, and primary open-angle glaucoma..
Ophthalmic Genet. 39(5), 603-609.
(2018).
(2009). Nichtendemischer erythrodermischer Pemphigus foliaceus: Ein Fall mit verzögerter Diagnose und Response auf Rituximab..
J Dtsch Dermatol Ges. 17(5), 537-539.
(2019). Non-endemic erythrodermic pemphigus foliaceus: a case with delayed diagnosis and response to rituximab..
J Dtsch Dermatol Ges. 17(5), 537-539.
(2019).
(2023).
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome..
Hum Mol Genet. 28(15), 2531-2548.
(2019).
(2019).
Validation of the TAGAP rs212389 polymorphism in rheumatoid arthritis susceptibility..
Joint Bone Spine. 80(5), 543-4.
(2013).