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Page 1
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.
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.
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
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
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: loules g. Allergy. 2018 Aug;73(8):1751-1753. doi: 10.1111/all.13324. Allergy. 2018. PMID: 30009523 No abstract available.
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.
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.
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.
CDKN2A copy number alteration in bladder cancer: Integrative analysis in patient-derived xenografts and cancer patients.
Papadimitriou MA, Pilala KM, Panoutsopoulou K, Levis P, Kotronopoulos G, Kanaki Z, Loules G, Zamanakou M, Linardoutsos D, Sideris DC, Stravodimos K, Klinakis A, Scorilas A, Avgeris M. Papadimitriou MA, et al. Among authors: loules g. Mol Ther Oncol. 2024 May 24;32(2):200818. doi: 10.1016/j.omton.2024.200818. eCollection 2024 Jun 20. Mol Ther Oncol. 2024. PMID: 38966038 Free PMC article.
20 results