Deltas CC - Search Results

1

Presymptomatic molecular diagnosis of autosomal dominant polycystic kidney disease using PKD1- and PKD2-linked markers in Cypriot families.

Deltas CC, Christodoulou K, Tjakouri C, Pierides A. Deltas CC, et al. Clin Genet. 1996 Jul;50(1):10-8. doi: 10.1111/j.1399-0004.1996.tb02339.x. Clin Genet. 1996. PMID: 8891380

2

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein.

Mochizuki T, Wu G, Hayashi T, Xenophontos SL, Veldhuisen B, Saris JJ, Reynolds DM, Cai Y, Gabow PA, Pierides A, Kimberling WJ, Breuning MH, Deltas CC, Peters DJ, Somlo S. Mochizuki T, et al. Among authors: deltas cc. Science. 1996 May 31;272(5266):1339-42. doi: 10.1126/science.272.5266.1339. Science. 1996. PMID: 8650545

3

Detection of a novel nonsense mutation and an intragenic polymorphism in the PKD1 gene of a Cypriot family with autosomal dominant polycystic kidney disease.

Neophytou P, Constantinides R, Lazarou A, Pierides A, Deltas CC. Neophytou P, et al. Among authors: deltas cc. Hum Genet. 1996 Oct;98(4):437-42. doi: 10.1007/s004390050235. Hum Genet. 1996. PMID: 8792818

4

New amino acid polymorphism, Ala/Val4058, in exon 45 of the polycystic kidney disease 1 gene: evolution of alleles.

Constantinides R, Xenophontos S, Neophytou P, Nomura S, Pierides A, Deltas CC. Constantinides R, et al. Among authors: deltas cc. Hum Genet. 1997 May;99(5):644-7. doi: 10.1007/s004390050421. Hum Genet. 1997. PMID: 9150733

5

A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).

Xenophontos S, Constantinides R, Hayashi T, Mochizuki T, Somlo S, Pierides A, Deltas CC. Xenophontos S, et al. Among authors: deltas cc. Hum Mol Genet. 1997 Jun;6(6):949-52. doi: 10.1093/hmg/6.6.949. Hum Mol Genet. 1997. PMID: 9175744

6

Clinical aspects of cystinuria.

Pierides AM, Deltas CC. Pierides AM, et al. Among authors: deltas cc. Contrib Nephrol. 1997;122:167-72. doi: 10.1159/000059895. Contrib Nephrol. 1997. PMID: 9399060 No abstract available.

7

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

Stavrou C, Pierides A, Zouvani I, Kyriacou K, Antignac C, Neophytou P, Christodoulou K, Deltas CC. Stavrou C, et al. Among authors: deltas cc. Am J Med Genet. 1998 May 1;77(2):149-54. doi: 10.1002/(sici)1096-8628(19980501)77:2<149::aid-ajmg8>3.0.co;2-n. Am J Med Genet. 1998. PMID: 9605289

8

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

Fuchshuber A, Deltas CC, Berthold S, Stavrou C, Vollmer M, Burton C, Feest T, Krieter D, Gal A, Brandis M, Pierides A, Hildebrandt F. Fuchshuber A, et al. Among authors: deltas cc. Nephrol Dial Transplant. 1998 Aug;13(8):1955-7. doi: 10.1093/ndt/13.8.1955. Nephrol Dial Transplant. 1998. PMID: 9719147

9

Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1.

Koptides M, Constantinides R, Kyriakides G, Hadjigavriel M, Patsalis PC, Pierides A, Deltas CC. Koptides M, et al. Among authors: deltas cc. Hum Genet. 1998 Dec;103(6):709-17. doi: 10.1007/s004390050896. Hum Genet. 1998. PMID: 9921908

10

Autosomal dominant polycystic kidney disease-type 2. Ultrasound, genetic and clinical correlations.

Demetriou K, Tziakouri C, Anninou K, Eleftheriou A, Koptides M, Nicolaou A, Deltas CC, Pierides A. Demetriou K, et al. Among authors: deltas cc. Nephrol Dial Transplant. 2000 Feb;15(2):205-11. doi: 10.1093/ndt/15.2.205. Nephrol Dial Transplant. 2000. PMID: 10648666

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