Deltas C - Search Results

1

Cystic diseases of the kidney: molecular biology and genetics.

Deltas C, Papagregoriou G. Deltas C, et al. Arch Pathol Lab Med. 2010 Apr;134(4):569-82. doi: 10.5858/134.4.569. Arch Pathol Lab Med. 2010. PMID: 20367309 Free article. Review.

2

Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.

Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Lipska-Ziętkiewicz BS. Savige J, et al. Among authors: deltas c. Eur J Hum Genet. 2024 Jan;32(1):132. doi: 10.1038/s41431-023-01288-x. Eur J Hum Genet. 2024. PMID: 36721056 Free PMC article. No abstract available.

3

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

4

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

5

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

6

Autosomal dominant polycystic kidney disease: molecular genetics and molecular pathogenesis.

Koptides M, Deltas CC. Koptides M, et al. Among authors: deltas cc. Hum Genet. 2000 Aug;107(2):115-26. doi: 10.1007/s004390000347. Hum Genet. 2000. PMID: 11030408 Review.

7

Mutations of the human polycystic kidney disease 2 (PKD2) gene.

Deltas CC. Deltas CC. Hum Mutat. 2001;18(1):13-24. doi: 10.1002/humu.1145. Hum Mutat. 2001. PMID: 11438989 Review.

8

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

Koptides M, Mean R, Stavrou C, Pierides A, Demetriou K, Nakayama T, Hildebrandt F, Fuchshuber A, Deltas CC. Koptides M, et al. Among authors: deltas cc. Mol Cell Probes. 2001 Dec;15(6):357-61. doi: 10.1006/mcpr.2001.0381. Mol Cell Probes. 2001. PMID: 11851379

9

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

Stavrou C, Koptides M, Tombazos C, Psara E, Patsias C, Zouvani I, Kyriacou K, Hildebrandt F, Christofides T, Pierides A, Deltas CC. Stavrou C, et al. Among authors: deltas cc. Kidney Int. 2002 Oct;62(4):1385-94. doi: 10.1111/j.1523-1755.2002.kid581.x. Kidney Int. 2002. PMID: 12234310 Free article.

10

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

Stavrou C, Deltas CC, Christophides TC, Pierides A. Stavrou C, et al. Among authors: deltas cc. Nephrol Dial Transplant. 2003 Oct;18(10):2165-9. doi: 10.1093/ndt/gfg196. Nephrol Dial Transplant. 2003. PMID: 13679497

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