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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: psarros f. Gene. 2018 Aug 15;667:76-82. doi: 10.1016/j.gene.2018.05.029. Epub 2018 May 16. Gene. 2018. PMID: 29753808
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: psarros f. 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.
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: psarros f. 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
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: psarros f. 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.
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: psarros f. 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.
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: psarros f. Front Allergy. 2022 Jul 7;3:868185. doi: 10.3389/falgy.2022.868185. eCollection 2022. Front Allergy. 2022. PMID: 35873600 Free PMC article.
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: psarros f. J Clin Med. 2020 Oct 23;9(11):3402. doi: 10.3390/jcm9113402. J Clin Med. 2020. PMID: 33114181 Free PMC article.
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema.
Germenis AE, Loules G, Zamanakou M, Psarros F, González-Quevedo T, Speletas M, Bork K, Wulff K, Steinmüller-Magin L, Braenne I, Staubach-Renz P, Witzke G, Hardt J. Germenis AE, et al. Among authors: psarros f. Allergy. 2018 Aug;73(8):1751-1753. doi: 10.1111/all.13324. Allergy. 2018. PMID: 30009523 No abstract available.
34 results