Filadelfia Komianou

A Novel Point Mutation in the DNA-Binding Domain (DBD) of the Human Glucocorticoid Receptor Causes Primary Generalized Glucocorticoid Resistance by Disrupting the Hydrophobic Structure of its DBD

Michael L. Roberts, Tomoshige Kino, Nicolas C. Nicolaides et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 43 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Frequent <i><scp>COL4</scp></i> mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis

L. Papazachariou, Gregory Papagregoriou, Despina Hadjipanagi et al. · Clinical Genetics · 2017 · 40 citations

Medicine, Genetics, Molecular Genetics +16

The Alport nephropathy: clinicopathological correlations

Richard H. White, F. Raafat, David V. Milford et al. · Pediatric Nephrology · 2005 · 22 citations

Medicine, Nephrology, Pathology +11

Psychomotor development in congenital hypothyroidism

Filadelfia Komianou, G. Makaronis, J. Lambadaridis et al. · European Journal of Pediatrics · 1988 · 21 citations

Medicine, Endocrinology, Human Development +13

Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms’ tumor 1 (WT1) gene

Spyridon Megremis, Andromachi Mitsioni, Irene Fylaktou et al. · European Journal of Pediatrics · 2011 · 15 citations

Medicine, Genetics, Pediatrics +16