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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
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73 results
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Page 1
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.
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
Repeated leftover serosurvey of SARS-CoV-2 IgG antibodies, Greece, March and April 2020.
Bogogiannidou Z, Vontas A, Dadouli K, Kyritsi MA, Soteriades S, Nikoulis DJ, Mouchtouri VΑ, Koureas M, Kazakos EI, Spanos EG, Gioula G, Ntzani EE, Eleftheriou AA, Vatopoulos A, Petinaki E, Papaevangelou V, Speletas M, Tsiodras S, Hadjichristodoulou C. Bogogiannidou Z, et al. Among authors: speletas m. Euro Surveill. 2020 Aug;25(31):2001369. doi: 10.2807/1560-7917.ES.2020.25.31.2001369. Euro Surveill. 2020. PMID: 32762796 Free PMC article.
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.
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.
Loules G, Parsopoulou F, Zamanakou M, Csuka D, Bova M, González-Quevedo T, Psarros F, Porebski G, Speletas M, Firinu D, Del Giacco S, Suffritti C, Makris M, Vatsiou S, Zanichelli A, Farkas H, Germenis AE. Loules G, et al. Among authors: speletas m. J Clin Med. 2020 Oct 23;9(11):3402. doi: 10.3390/jcm9113402. J Clin Med. 2020. PMID: 33114181 Free PMC article.
A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency.
Vatsiou S, Zamanakou M, Loules G, Psarros F, Parsopoulou F, Csuka D, Valerieva A, Staevska M, Porebski G, Obtulowicz K, Magerl M, Maurer M, Speletas M, Farkas H, Germenis AE. Vatsiou S, et al. Among authors: speletas m. Allergol Int. 2020 Jul;69(3):443-449. doi: 10.1016/j.alit.2019.12.009. Epub 2020 Jan 17. Allergol Int. 2020. PMID: 31959500 Free article.
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.
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