K. Dermitzaki

Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene

K. Stylianou, I. Petrakis, I. Zaganas, 2022, BMC Nephrology.

Cardiorenal Syndrome: Challenges in Everyday Clinical Practice and Key Points towards a Better Management

K. Stylianou, I. Petrakis, E. Lioudaki, 2023, Journal of clinical medicine.

The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone

K. Stylianou, I. Petrakis, I. Zaganas, 2022, International journal of molecular sciences.

Cytokinetic and cytotoxic effects of urea on HeLa cells in suspension cultures.

A. Glinos, G. Bardi, M. Talieri, 1983, Journal of the National Cancer Institute.

Mixed lineage leukemia with cytogenetically unrelated abnormal clones.

N. Pandis, G. Bardi, M. Stamatellou, 1989, Cancer genetics and cytogenetics.