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Did you mean gedeon lobules (3 results)?
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: loules g. Front Allergy. 2022 Jul 7;3:868185. doi: 10.3389/falgy.2022.868185. eCollection 2022. Front Allergy. 2022. PMID: 35873600 Free PMC article.
Foxp3 expression in human cancer cells.
Karanikas V, Speletas M, Zamanakou M, Kalala F, Loules G, Kerenidi T, Barda AK, Gourgoulianis KI, Germenis AE. Karanikas V, et al. Among authors: loules g. J Transl Med. 2008 Apr 22;6:19. doi: 10.1186/1479-5876-6-19. J Transl Med. 2008. PMID: 18430198 Free PMC article.
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: loules g. 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.
Fabry disease due to D313Y and novel GLA mutations.
Koulousios K, Stylianou K, Pateinakis P, Zamanakou M, Loules G, Manou E, Kyriklidou P, Katsinas C, Ouzouni A, Kyriazis J, Speletas M, Germenis AE. Koulousios K, et al. Among authors: loules g. BMJ Open. 2017 Oct 6;7(10):e017098. doi: 10.1136/bmjopen-2017-017098. BMJ Open. 2017. PMID: 28988177 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. J Clin Med. 2020 Oct 23;9(11):3402. doi: 10.3390/jcm9113402. J Clin Med. 2020. PMID: 33114181 Free PMC article.
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: loules g. 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
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: loules g. 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.
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. Gene. 2018 Aug 15;667:76-82. doi: 10.1016/j.gene.2018.05.029. Epub 2018 May 16. Gene. 2018. PMID: 29753808
12 results