Speletas M - Search Results

1

MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates.

Speletas M, Gounaris A, Sevdali E, Kompoti M, Konstantinidi K, Sokou R, Tsitsami E, Germenis AE. Speletas M, et al. J Immunol Res. 2015;2015:478412. doi: 10.1155/2015/478412. Epub 2015 Mar 24. J Immunol Res. 2015. PMID: 25879044 Free PMC article.

2

Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.

Speletas M, Kioumi A, Loules G, Hytiroglou P, Tsitouridis J, Christakis J, Germenis AE. Speletas M, et al. Blood Cells Mol Dis. 2008 May-Jun;40(3):353-9. doi: 10.1016/j.bcmd.2007.09.011. Epub 2007 Nov 9. Blood Cells Mol Dis. 2008. PMID: 17997113

3

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. 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.

4

Foxp3 expression in human cancer cells.

Karanikas V, Speletas M, Zamanakou M, Kalala F, Loules G, Kerenidi T, Barda AK, Gourgoulianis KI, Germenis AE. Karanikas V, et al. Among authors: speletas m. J Transl Med. 2008 Apr 22;6:19. doi: 10.1186/1479-5876-6-19. J Transl Med. 2008. PMID: 18430198 Free PMC article.

5

TLR2 and TLR4 polymorphisms in familial Mediterranean fever.

Speletas M, Kalala F, Mitroulis I, Papadopoulos V, Merentiti V, Germenis AE, Ritis K. Speletas M, et al. Hum Immunol. 2009 Sep;70(9):750-3. doi: 10.1016/j.humimm.2009.05.004. Epub 2009 May 13. Hum Immunol. 2009. PMID: 19445990

6

Hereditary angioedema in Greek families caused by novel and recurrent mutations.

Speletas M, Boukas K, Papadopoulou-Alataki E, Tsitsami E, Germenis AE. Speletas M, et al. Hum Immunol. 2009 Nov;70(11):925-9. doi: 10.1016/j.humimm.2009.08.010. Epub 2009 Aug 23. Hum Immunol. 2009. PMID: 19706314

7

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: speletas m. Neurol Sci. 2010 Jun;31(3):393-7. doi: 10.1007/s10072-009-0201-0. Epub 2009 Dec 2. Neurol Sci. 2010. PMID: 19953284

8

Association of TLR4-T399I polymorphism with chronic obstructive pulmonary disease in smokers.

Speletas M, Merentiti V, Kostikas K, Liadaki K, Minas M, Gourgoulianis K, Germenis AE. Speletas M, et al. Clin Dev Immunol. 2009;2009:260286. doi: 10.1155/2009/260286. Epub 2010 Feb 15. Clin Dev Immunol. 2009. PMID: 20169003 Free PMC article.

9

Toll-like receptor 4 gene (TLR4), but not TLR2, polymorphisms modify the risk of tonsillar disease due to Streptococcus pyogenes and Haemophilus influenzae.

Liadaki K, Petinaki E, Skoulakis C, Tsirevelou P, Klapsa D, Germenis AE, Speletas M. Liadaki K, et al. Among authors: speletas m. Clin Vaccine Immunol. 2011 Feb;18(2):217-22. doi: 10.1128/CVI.00460-10. Epub 2010 Dec 15. Clin Vaccine Immunol. 2011. PMID: 21159925 Free PMC article.

10

SLC40A1-R178G mutation and ferroportin disease.

Speletas M, Onoufriadis E, Kioumi A, Germenis AE. Speletas M, et al. J Hepatol. 2011 Sep;55(3):730-731. doi: 10.1016/j.jhep.2011.01.024. Epub 2011 Feb 12. J Hepatol. 2011. PMID: 21320560 Free article. No abstract available.

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