C. Stavrou

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

G. Mollet, C. Antignac, C. Antignac, 2001, Journal of the American Society of Nephrology : JASN.

An International Cohort Study of Autosomal Dominant Tubulointerstitial Kidney Disease due to REN Mutations Identifies Distinct Clinical Subtypes.

K. Tory, C. Shaw-Smith, A. Jakubowska, 2020, Kidney international.

Outcome of kidney transplantation in autosomal dominant medullary cystic kidney disease type 1.

A. Pierides, C. Deltas, C. Stavrou, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families.

K. Kyriacou, F. Hildebrandt, A. Pierides, 2002, Kidney international.

X‐linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5

K. Voskarides, A. Pierides, C. Deltas, 2012, Clinical genetics.

Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1.

F. Hildebrandt, A. Pierides, C. Deltas, 2001, Molecular and cellular probes.

Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease.

A. Pierides, C. Deltas, A. Eleftheriou, 1998, Human molecular genetics.

Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1.

K. Kyriacou, C. Antignac, A. Pierides, 1998, American journal of medical genetics.

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?

K. Voskarides, A. Pierides, C. Deltas, 2018, BMC Nephrology.

Frequency of COL4A3/COL4A4 Mutations amongst Families Segregating Glomerular Microscopic Hematuria and Evidence for Activation of the Unfolded Protein Response. Focal and Segmental Glomerulosclerosis Is a Frequent Development during Ageing

K. Voskarides, A. Pierides, C. Deltas, 2014, PloS one.

Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneity.

F. Hildebrandt, T. Feest, A. Pierides, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.