Christoforos Stavrou

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

Christoforos Stavrou, Michael Koptides, Christos Tombazos et al. · Kidney International · 2002 · 76 citations

Urology, Molecular Findings, Mendelian Disorder +8

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

Louiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri et al. · PLoS ONE · 2014 · 69 citations · Full text

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

Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi et al. · BMC Nephrology · 2018 · 42 citations · Full text

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

P Demosthenous, Konstantinos Voskarides, Kostas Stylianou et al. · Clinical Genetics · 2011 · 41 citations

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Martina Živná, Kendrah Kidd, Mohamad Zaidan et al. · Kidney International · 2020 · 39 citations · Full text

Glomerular Disease, Glomerulonephritis, Urology +11