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International Angiology : a Journal of the International Union of Angiology|September 15, 2005
The MTHFR 677TT and 677CT/1298AC genotypes in Cypriot patients may be predisposing to hypertensive nephrosclerosis and chronic renal failureP Koupepidou, C Deltas, T C Christofides, et al.
Human Genetics|May 1, 1997
New amino acid polymorphism, Ala/Val4058, in exon 45 of the polycystic kidney disease 1 gene: evolution of allelesR Constantinides, S Xenophontos, P Neophytou, et al.
Clinical Genetics|January 26, 2006
Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 geneM Feldman, M Prikis, Y Athanasiou, et al.
Human Molecular Genetics|June 1, 1997
A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2)S Xenophontos, R Constantinides, T Hayashi, et al.
Human Mutation|August 3, 2000
Screening of the PKD1 duplicated region reveals multiple single nucleotide polymorphisms and a de novo mutation in Hellenic polycystic kidney disease familiesM Koptides, R Mean, K Demetriou, et al.
American Journal of Medical Genetics|May 30, 1998
Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1C Stavrou, A Pierides, I Zouvani, et al.
Human Genetics|January 28, 1999
Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1M Koptides, R Constantinides, G Kyriakides, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 29, 2000
Autosomal dominant polycystic kidney disease-type 2. Ultrasound, genetic and clinical correlationsK Demetriou, C Tziakouri, K Anninou, et al.
Journal of Nephrology|March 12, 2013
Renal graft outcome in autosomal dominant medullary cystic kidney disease type 1Andreas P Soloukides, Dimitrios-Anestis D Moutzouris, Gregory N Papagregoriou, et al.
Molecular and Cellular Probes|February 20, 2002
Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1M Koptides, R Mean, C Stavrou, et al.
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