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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1998 2
2000 3
2001 2
2002 3
2003 3
2005 2
2006 3
2007 8
2008 5
2009 8
2010 3
2011 7
2012 4
2013 7
2014 6
2015 6
2016 4
2017 7
2018 4
2019 2
2020 6
2021 13
2022 14
2023 10
2024 1

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119 results

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Page 1
BAFF receptor polymorphisms and deficiency in humans.
Sevdali E, Block Saldana V, Speletas M, Eibel H. Sevdali E, et al. Among authors: speletas m. Curr Opin Immunol. 2021 Aug;71:103-110. doi: 10.1016/j.coi.2021.06.008. Epub 2021 Jul 24. Curr Opin Immunol. 2021. PMID: 34311146 Review.
Genetics of Hereditary Angioedema Revisited.
Germenis AE, Speletas M. Germenis AE, et al. Among authors: speletas m. Clin Rev Allergy Immunol. 2016 Oct;51(2):170-82. doi: 10.1007/s12016-016-8543-x. Clin Rev Allergy Immunol. 2016. PMID: 27116602 Review.
Innate Immune Gene Polymorphisms and COVID-19 Prognosis.
Bakaros E, Voulgaridi I, Paliatsa V, Gatselis N, Germanidis G, Asvestopoulou E, Alexiou S, Botsfari E, Lygoura V, Tsachouridou O, Mimtsoudis I, Tseroni M, Sarrou S, Mouchtouri VA, Dadouli K, Kalala F, Metallidis S, Dalekos G, Hadjichristodoulou C, Speletas M. Bakaros E, et al. Among authors: speletas m. Viruses. 2023 Aug 22;15(9):1784. doi: 10.3390/v15091784. Viruses. 2023. PMID: 37766191 Free PMC article.
TNFRSF13C/BAFFR P21R and H159Y polymorphisms in multiple sclerosis.
Ntellas P, Dardiotis E, Sevdali E, Siokas V, Aloizou AM, Tsinti G, Germenis AE, Hadjigeorgiou GM, Eibel H, Speletas M. Ntellas P, et al. Among authors: speletas m. Mult Scler Relat Disord. 2020 Jan;37:101422. doi: 10.1016/j.msard.2019.101422. Epub 2019 Sep 30. Mult Scler Relat Disord. 2020. PMID: 32172995
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.
A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature.
Dardiotis E, Siokas V, Pantazi E, Dardioti M, Rikos D, Xiromerisiou G, Markou A, Papadimitriou D, Speletas M, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: speletas m. Neurobiol Aging. 2017 May;53:194.e13-194.e22. doi: 10.1016/j.neurobiolaging.2017.01.015. Epub 2017 Jan 20. Neurobiol Aging. 2017. PMID: 28214109 Review.
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).
Parsopoulou F, Loules G, Zamanakou M, Csuka D, Szilagyi A, Kompoti M, Porebski G, Psarros F, Magerl M, Valerieva A, Staevska M, Obtulowicz K, Maurer M, Speletas M, Farkas H, Germenis AE. Parsopoulou F, et al. Among authors: speletas m. Front Allergy. 2022 Jul 7;3:868185. doi: 10.3389/falgy.2022.868185. eCollection 2022. Front Allergy. 2022. PMID: 35873600 Free PMC article.
119 results