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Page 1
Detection of two novel alleles, HLA-A*02:943 and -B*51:104:02, in Greek cord blood units.
HLA. 2021 Mar;97(3):214-215. doi: 10.1111/tan.14138. Epub 2020 Nov 25.
HLA. 2021.
PMID: 33191636
Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?
Germenis AE, Vatsiou S, Csuka D, Zamanakou M, Farkas H.
Germenis AE, et al. Among authors: vatsiou s.
J Clin Immunol. 2021 Jan;41(1):248-250. doi: 10.1007/s10875-020-00887-3. Epub 2020 Oct 9.
J Clin Immunol. 2021.
PMID: 33034800
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: vatsiou s.
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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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
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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.
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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