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2018 | 1 |
2020 | 3 |
2022 | 2 |
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Page 1
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.
Front Allergy. 2022 Mar 31;3:835503. doi: 10.3389/falgy.2022.835503. eCollection 2022.
Front Allergy. 2022.
PMID: 35958943
Free PMC article.
Review.
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.
Front Allergy. 2022 Jul 7;3:868185. doi: 10.3389/falgy.2022.868185. eCollection 2022.
Front Allergy. 2022.
PMID: 35873600
Free PMC article.
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Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients.
Parsopoulou F, Charignon D, Tengo M, Psarros F, Maas C, Gonzalez-Quevedo T, Drouet C, Germenis AE, Ghannam A.
Parsopoulou F, et al.
Allergy. 2020 Aug;75(8):2099-2102. doi: 10.1111/all.14280. Epub 2020 Apr 6.
Allergy. 2020.
PMID: 32181895
No abstract available.
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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: parsopoulou f.
J Clin Med. 2020 Oct 23;9(11):3402. doi: 10.3390/jcm9113402.
J Clin Med. 2020.
PMID: 33114181
Free PMC article.
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Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.
Vincent D, Parsopoulou F, Martin L, Gaboriaud C, Demongeot J, Loules G, Fischer S, Cichon S, Germenis AE, Ghannam A, Drouet C.
Vincent D, et al. Among authors: parsopoulou f.
J Allergy Clin Immunol Glob. 2024 Feb 1;3(2):100223. doi: 10.1016/j.jacig.2024.100223. eCollection 2024 May.
J Allergy Clin Immunol Glob. 2024.
PMID: 38445235
Free PMC article.
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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: parsopoulou f.
Gene. 2018 Aug 15;667:76-82. doi: 10.1016/j.gene.2018.05.029. Epub 2018 May 16.
Gene. 2018.
PMID: 29753808
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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: parsopoulou 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.
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