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2018 1
2020 4
2021 2
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Page 1
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: vatsiou s. J Clin Med. 2020 Oct 23;9(11):3402. doi: 10.3390/jcm9113402. J Clin Med. 2020. PMID: 33114181 Free PMC article.
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: vatsiou s. Gene. 2018 Aug 15;667:76-82. doi: 10.1016/j.gene.2018.05.029. Epub 2018 May 16. Gene. 2018. PMID: 29753808