Browsing by Author Mitsioni, A.

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TitleAuthor(s)Issue date
Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformationsBouba, I.; Siomou, E.; Stefanidis, C. J.; Emmanouilidou, A.; Galidi, A.; Hatzi, E.; Markoula, S.; Mitsioni, A.; Siamopoulou, A.; Georgiou, I.24-Nov-2015
Serum osteoprotegerin, RANKL and fibroblast growth factor-23 in children with chronic kidney diseaseSiomou, E.; Challa, A.; Printza, N.; Giapros, V.; Petropoulou, F.; Mitsioni, A.; Papachristou, F.; Stefanidis, C. J.24-Nov-2015