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 Germenis, Anastasios E [Clear All Filters]
Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV..
Blood Cells Mol Dis. 40(3), 353-9.
(2008). Foxp3 expression in liver correlates with the degree but not the cause of inflammation..
Mediators Inflamm. 2011, 827565.
(2011). Hereditary angioedema in Greece: the first results of the greek hereditary angioedema registry..
Int Arch Allergy Immunol. 164(4), 326-32.
(2014). Hereditary angioedema in Greek families caused by novel and recurrent mutations..
Hum Immunol. 70(11), 925-9.
(2009). Liver FOXP3 and PD1/PDL1 Expression is Down-Regulated in Chronic HBV Hepatitis on Maintained Remission Related to the Degree of Inflammation..
Front Immunol. 4, 207.
(2013). Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies..
J Immunol Res. 2017, 1514294.
(2017). The role of the NLRP3 inflammasome and the activation of IL-1β in the pathogenesis of chronic viral hepatic inflammation..
Cytokine. 110, 389-396.
(2018). Survivin isoform expression patterns in CML patients correlate with resistance to imatinib and progression, but do not trigger cytolytic responses..
Clin Immunol. 139(2), 155-63.
(2011). TACI expression and signaling in chronic lymphocytic leukemia..
J Immunol Res. 2015, 478753.
(2015). TGF-β signaling is activated in patients with chronic HBV infection and repressed by SMAD7 overexpression after successful antiviral treatment..
Inflamm Res. 65(5), 355-65.
(2016). TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies..
J Clin Immunol. 31(4), 550-9.
(2011).