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

Year Number of Results
2002 2
2003 3
2006 3
2007 4
2008 3
2009 7
2010 2
2011 7
2012 3
2013 5
2014 5
2015 5
2016 3
2017 6
2018 3
2019 3
2020 7
2021 12
2022 14
2023 10
2024 1

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96 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.
International Consensus on the Use of Genetics in the Management of Hereditary Angioedema.
Germenis AE, Margaglione M, Pesquero JB, Farkas H, Cichon S, Csuka D, Lera AL, Rijavec M, Jolles S, Szilagyi A, Trascasa ML, Veronez CL, Drouet C, Zamanakou M; Hereditary Angioedema International Working Group. Germenis AE, et al. J Allergy Clin Immunol Pract. 2020 Mar;8(3):901-911. doi: 10.1016/j.jaip.2019.10.004. Epub 2019 Oct 24. J Allergy Clin Immunol Pract. 2020. PMID: 31669336 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.
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations.
Thalhammer J, Kindle G, Nieters A, Rusch S, Seppänen MRJ, Fischer A, Grimbacher B, Edgar D, Buckland M, Mahlaoui N, Ehl S; European Society for Immunodeficiencies Registry Working Party. Thalhammer J, et al. J Allergy Clin Immunol. 2021 Nov;148(5):1332-1341.e5. doi: 10.1016/j.jaci.2021.04.015. Epub 2021 Apr 23. J Allergy Clin Immunol. 2021. PMID: 33895260
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
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.
96 results