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Page 1
3β-Hydroxysteroid Dehydrogenase Type 2 (3βHSD2) Deficiency due to a Novel Compound Heterozygosity of a Missense Mutation (p.Thr259Met) and Frameshift Deletion (p.Lys273ArgFs*7) in an Undervirilized Infant Male with Salt Wasting.
Leka-Emiri S, Taibi L, Mavroeidi V, Vlachopapadopoulou EA, Kafetzi M, Michalacos S, de Roux N. Leka-Emiri S, et al. Among authors: mavroeidi v. Sex Dev. 2022;16(1):64-69. doi: 10.1159/000519062. Epub 2021 Oct 8. Sex Dev. 2022. PMID: 34628416
Distinctive features of pancreatic neuroendocrine neoplasms exhibiting an increment in proliferative activity during the course of the disease.
Alexandraki KI, Kaltsatou M, Kyriakopoulos G, Mavroeidi V, Kostopoulou A, Atlan K, Theocharis S, Rindi G, Grossman AB, Grozinsky-Glasberg S, Kaltsas GA. Alexandraki KI, et al. Among authors: mavroeidi v. Endocrine. 2021 Apr;72(1):279-286. doi: 10.1007/s12020-020-02540-w. Epub 2020 Nov 11. Endocrine. 2021. PMID: 33175321
Rapamycin induced ultrastructural and molecular alterations in glomerular podocytes in healthy mice.
Stylianou K, Petrakis I, Mavroeidi V, Stratakis S, Kokologiannakis G, Lioudaki E, Liotsi C, Kroustalakis N, Vardaki E, Stratigis S, Perakis K, Kyriazis J, Nakopoulou L, Daphnis E. Stylianou K, et al. Among authors: mavroeidi v. Nephrol Dial Transplant. 2012 Aug;27(8):3141-8. doi: 10.1093/ndt/gfr791. Epub 2012 Jan 30. Nephrol Dial Transplant. 2012. PMID: 22290989
15 results