Nucleotide Variations in the <i>NPHS2</i> Gene in Greek Children with Steroid-Resistant Nephrotic SyndromeSpyridon Megremis, Joanne Traeger‐Synodinos, Sofia Kitsiou-Tzelli et al.|Genetic Testing and Molecular Biomarkers|2009Cited by 19
Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms’ tumor 1 (WT1) geneSpyridon Megremis, Joanne Traeger‐Synodinos, Andromachi Mitsioni et al.|European Journal of Pediatrics|2011Cited by 15
Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutationSophia Kitsiou‐Tzeli, Emmanuel Kanavakis, Maria V. Deligiorgi et al.|HORMONES|2012Cited by 9
Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotypeIrene Fylaktou, Joanne Traeger‐Synodinos, Emmanuel Kanavakis et al.|Journal of Genetics|2013Cited by 2