Koptides M - Search Results

1

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: koptides m. Nephrol Dial Transplant. 2000 Feb;15(2):205-11. doi: 10.1093/ndt/15.2.205. Nephrol Dial Transplant. 2000. PMID: 10648666

2

A family with the branchio-oto-renal syndrome: clinical and genetic correlations.

Pierides AM, Athanasiou Y, Demetriou K, Koptides M, Deltas CC. Pierides AM, et al. Among authors: koptides m. Nephrol Dial Transplant. 2002 Jun;17(6):1014-8. doi: 10.1093/ndt/17.6.1014. Nephrol Dial Transplant. 2002. PMID: 12032190

3

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: koptides m. Kidney Int. 2002 Oct;62(4):1385-94. doi: 10.1111/j.1523-1755.2002.kid581.x. Kidney Int. 2002. PMID: 12234310 Free article.

4

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. Hum Genet. 1998 Dec;103(6):709-17. doi: 10.1007/s004390050896. Hum Genet. 1998. PMID: 9921908

5

Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease.

Koptides M, Mean R, Demetriou K, Pierides A, Deltas CC. Koptides M, et al. Hum Mol Genet. 2000 Feb 12;9(3):447-52. doi: 10.1093/hmg/9.3.447. Hum Mol Genet. 2000. PMID: 10655555

6

Screening of the PKD1 duplicated region reveals multiple single nucleotide polymorphisms and a de novo mutation in Hellenic polycystic kidney disease families.

Koptides M, Mean R, Demetriou K, Constantinides R, Pierides A, Harris PC, Deltas CC. Koptides M, et al. Hum Mutat. 2000 Aug;16(2):176. doi: 10.1002/1098-1004(200008)16:2<176::AID-HUMU11>3.0.CO;2-H. Hum Mutat. 2000. PMID: 10923040

7

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

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

8

Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families.

Bouba I, Koptides M, Mean R, Costi CE, Demetriou K, Georgiou I, Pierides A, Siamopoulos K, Deltas CC. Bouba I, et al. Among authors: koptides m. Eur J Hum Genet. 2001 Sep;9(9):677-84. doi: 10.1038/sj.ejhg.5200696. Eur J Hum Genet. 2001. PMID: 11571556

9

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. Mol Cell Probes. 2001 Dec;15(6):357-61. doi: 10.1006/mcpr.2001.0381. Mol Cell Probes. 2001. PMID: 11851379

10

Germinal and somatic mutations in the PKD2 gene of renal cysts in autosomal dominant polycystic kidney disease.

Koptides M, Hadjimichael C, Koupepidou P, Pierides A, Constantinou Deltas C. Koptides M, et al. Hum Mol Genet. 1999 Mar;8(3):509-13. doi: 10.1093/hmg/8.3.509. Hum Mol Genet. 1999. PMID: 9949210

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