Germenis A - Search Results

1

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene.

Daiou C, Christodoulou K, Xiromerisiou G, Panas M, Dardiotis E, Kladi A, Speletas M, Ntaios G, Papadimitriou A, Germenis A, Hadjigeorgiou GM. Daiou C, et al. Among authors: germenis a. Neurol Sci. 2010 Jun;31(3):393-7. doi: 10.1007/s10072-009-0201-0. Epub 2009 Dec 2. Neurol Sci. 2010. PMID: 19953284

2

TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders.

Speletas M, Liadaki K, Kalala F, Daiou C, Katodritou E, Mandala E, Korantzis I, Ritis K, Zintzaras E, Germenis AE. Speletas M, et al. Among authors: germenis ae. Thromb Res. 2008;122(1):27-32. doi: 10.1016/j.thromres.2007.09.016. Epub 2007 Nov 14. Thromb Res. 2008. PMID: 17999935 No abstract available.

3

Association between TLR2/TLR4 gene polymorphisms and COPD phenotype in a Greek cohort.

Apostolou A, Kerenidi T, Michopoulos A, Gourgoulianis KI, Noutsias M, Germenis AE, Speletas M. Apostolou A, et al. Among authors: germenis ae. Herz. 2017 Dec;42(8):752-757. doi: 10.1007/s00059-016-4510-9. Epub 2016 Dec 1. Herz. 2017. PMID: 27909766 English.

4

Rapid detection of MYD88-L265P mutation by PCR-RFLP in B-cell lymphoproliferative disorders.

Argentou N, Vassilopoulos G, Ioannou M, Germenis AE, Speletas M. Argentou N, et al. Among authors: germenis ae. Leukemia. 2014 Feb;28(2):447-9. doi: 10.1038/leu.2013.294. Epub 2013 Oct 18. Leukemia. 2014. PMID: 24135828 No abstract available.

5

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

Speletas M, Szilágyi Á, Csuka D, Koutsostathis N, Psarros F, Moldovan D, Magerl M, Kompoti M, Varga L, Maurer M, Farkas H, Germenis AE. Speletas M, et al. Among authors: germenis ae. Allergy. 2015 Dec;70(12):1661-4. doi: 10.1111/all.12714. Epub 2015 Aug 26. Allergy. 2015. PMID: 26248961

6

Cytokine levels in the sera of patients with idiopathic pulmonary fibrosis.

Tsoutsou PG, Gourgoulianis KI, Petinaki E, Germenis A, Tsoutsou AG, Mpaka M, Efremidou S, Molyvdas PA. Tsoutsou PG, et al. Among authors: germenis a. Respir Med. 2006 May;100(5):938-45. doi: 10.1016/j.rmed.2005.06.016. Epub 2005 Oct 19. Respir Med. 2006. PMID: 16236490 Free article.

7

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Farkas H, Martinez-Saguer I, Bork K, Bowen T, Craig T, Frank M, Germenis AE, Grumach AS, Luczay A, Varga L, Zanichelli A; HAWK. Farkas H, et al. Among authors: germenis ae. Allergy. 2017 Feb;72(2):300-313. doi: 10.1111/all.13001. Epub 2016 Sep 8. Allergy. 2017. PMID: 27503784 Free PMC article.

8

Downregulation of serum epidermal growth factor in patients with inflammatory bowel disease. Is there a link with mucosal damage?

Oikonomou KA, Kapsoritakis AN, Kapsoritaki AI, Manolakis AC, Tsiopoulos FD, Germenis AE, Potamianos SP. Oikonomou KA, et al. Among authors: germenis ae. Growth Factors. 2010 Dec;28(6):461-6. doi: 10.3109/08977194.2010.527967. Epub 2010 Oct 25. Growth Factors. 2010. PMID: 20969541

9

Neutrophil gelatinase-associated lipocalin (NGAL) in inflammatory bowel disease: association with pathophysiology of inflammation, established markers, and disease activity.

Oikonomou KA, Kapsoritakis AN, Theodoridou C, Karangelis D, Germenis A, Stefanidis I, Potamianos SP. Oikonomou KA, et al. Among authors: germenis a. J Gastroenterol. 2012 May;47(5):519-30. doi: 10.1007/s00535-011-0516-5. Epub 2011 Dec 27. J Gastroenterol. 2012. PMID: 22200942

10

Type I interferonopathy in a young adult.

Manoussakis MN, Mavragani CP, Nezos A, Zampeli E, Germenis A, Moutsopoulos HM. Manoussakis MN, et al. Among authors: germenis a. Rheumatology (Oxford). 2017 Dec 1;56(12):2241-2243. doi: 10.1093/rheumatology/kex316. Rheumatology (Oxford). 2017. PMID: 28968819 No abstract available.

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