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Hereditary angioedema: molecular and clinical differences among European populations.
Speletas M, Szilagyi A, Psarros F, Moldovan D, Magerl M, Kompoti M, Gramoustianou E, Bors A, Mihaly E, Tordai A, Avramouli A, Varga L, Maurer M, Farkas H, Germenis AE. Speletas M, et al. Among authors: germenis ae. J Allergy Clin Immunol. 2015 Feb;135(2):570-3. doi: 10.1016/j.jaci.2014.08.007. Epub 2014 Sep 23. J Allergy Clin Immunol. 2015. PMID: 25258140 No abstract available.
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.
Genetic Determinants of C1 Inhibitor Deficiency Angioedema Age of Onset.
Gianni P, Loules G, Zamanakou M, Kompoti M, Csuka D, Psarros F, Magerl M, Moldovan D, Maurer M, Speletas MG, Farkas H, Germenis AE. Gianni P, et al. Among authors: germenis ae. Int Arch Allergy Immunol. 2017;174(3-4):200-204. doi: 10.1159/000481987. Epub 2017 Nov 9. Int Arch Allergy Immunol. 2017. PMID: 29130992
Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.
Loules G, Zamanakou M, Parsopoulou F, Vatsiou S, Psarros F, Csuka D, Porebski G, Obtulowicz K, Valerieva A, Staevska M, López-Lera A, López-Trascasa M, Moldovan D, Magerl M, Maurer M, Speletas M, Farkas H, Germenis AE. Loules G, et al. Among authors: germenis ae. Gene. 2018 Aug 15;667:76-82. doi: 10.1016/j.gene.2018.05.029. Epub 2018 May 16. Gene. 2018. PMID: 29753808
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.
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: germenis ae. 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.
132 results