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

Year Number of Results
1987 1
1990 1
1991 1
1997 1
1999 1
2004 1
2005 3
2006 3
2007 9
2008 6
2009 4
2010 5
2011 5
2012 1
2013 5
2014 6
2015 11
2016 7
2017 8
2018 3
2019 4
2020 8
2021 6
2022 3
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83 results
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Page 1
Genetics of Hereditary Angioedema Revisited.
Germenis AE, Speletas M. Germenis AE, et al. 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.
The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency.
Zanichelli A, Farkas H, Bouillet L, Bara N, Germenis AE, Psarros F, Varga L, Andrási N, Boccon-Gibod I, Castiglioni Roffia M, Rutkowski M, Cancian M. Zanichelli A, et al. Among authors: germenis ae. Clin Rev Allergy Immunol. 2021 Aug;61(1):77-83. doi: 10.1007/s12016-021-08855-4. Epub 2021 Mar 31. Clin Rev Allergy Immunol. 2021. PMID: 33791951 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.
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: germenis ae. 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
83 results