van de Kar NCAJ - Search Results

1

Proposal for individualized dosing of eculizumab in atypical haemolytic uraemic syndrome: patient friendly and cost-effective.

Ter Avest M, Bouwmeester RN, Duineveld C, Wijnsma KL, Volokhina EB, van den Heuvel LPWJ, Burger DM, Wetzels JFM, van de Kar NCAJ, Ter Heine R; CUREiHUS study group. Ter Avest M, et al. Among authors: van de kar ncaj, van den heuvel lpwj. Nephrol Dial Transplant. 2023 Feb 13;38(2):362-371. doi: 10.1093/ndt/gfac056. Nephrol Dial Transplant. 2023. PMID: 35238929 Free PMC article.

2

Verocytotoxin inhibits mitogenesis and protein synthesis in purified human glomerular mesangial cells without affecting cell viability: evidence for two distinct mechanisms.

Van Setten PA, van Hinsbergh VW, Van den Heuvel LP, van der Velden TJ, van de Kar NC, Krebbers RJ, Karmali MA, Monnens LA. Van Setten PA, et al. J Am Soc Nephrol. 1997 Dec;8(12):1877-88. doi: 10.1681/ASN.V8121877. J Am Soc Nephrol. 1997. PMID: 9402090

3

Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.

Assink K, Schiphorst R, Allford S, Karpman D, Etzioni A, Brichard B, van de Kar N, Monnens L, van den Heuvel L. Assink K, et al. Kidney Int. 2003 Jun;63(6):1995-9. doi: 10.1046/j.1523-1755.63.6s.1.x. Kidney Int. 2003. PMID: 12753286 Free article.

4

[From gene to disease; congenital thrombotic thrombocytopenic purpura due to mutations in the ADAMTS13 gene].

Schiphorst RH, van de Kar NC, van den Heuvel LP. Schiphorst RH, et al. Ned Tijdschr Geneeskd. 2003 Dec 6;147(49):2422-4. Ned Tijdschr Geneeskd. 2003. PMID: 14694551 Review. Dutch.

5

A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome.

Geelen J, van den Dries K, Roos A, van de Kar N, de Kat Angelino C, Klasen I, Monnens L, van den Heuvel L. Geelen J, et al. Pediatr Nephrol. 2007 Mar;22(3):371-5. doi: 10.1007/s00467-006-0320-2. Epub 2006 Nov 15. Pediatr Nephrol. 2007. PMID: 17106690

6

Rituximab in minimal change nephropathy and focal segmental glomerulosclerosis: report of four cases and review of the literature.

Peters HP, van de Kar NC, Wetzels JF. Peters HP, et al. Neth J Med. 2008 Nov;66(10):408-15. Neth J Med. 2008. PMID: 19011266 Free article.

7

Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS).

Westra D, Volokhina E, van der Heijden E, Vos A, Huigen M, Jansen J, van Kaauwen E, van der Velden T, van de Kar N, van den Heuvel L. Westra D, et al. Nephrol Dial Transplant. 2010 Jul;25(7):2195-202. doi: 10.1093/ndt/gfq010. Epub 2010 Jan 26. Nephrol Dial Transplant. 2010. PMID: 20106822

8

A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome.

Westra D, Wetzels JF, Volokhina EB, van den Heuvel LP, van de Kar NC. Westra D, et al. Neth J Med. 2012 Apr;70(3):121-9. Neth J Med. 2012. PMID: 22516576 Free article. Review.

9

Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding.

Volokhina E, Westra D, Xue X, Gros P, van de Kar N, van den Heuvel L. Volokhina E, et al. Pediatr Nephrol. 2012 Sep;27(9):1519-24. doi: 10.1007/s00467-012-2183-z. Epub 2012 Jun 6. Pediatr Nephrol. 2012. PMID: 22669319 Free PMC article.

10

Living kidney transplantation in adult patients with atypical haemolytic uraemic syndrome.

Verhave JC, Westra D, van Hamersvelt HW, van Helden M, van de Kar NC, Wetzels JF. Verhave JC, et al. Neth J Med. 2013 Sep;71(7):342-7. Neth J Med. 2013. PMID: 24038559 Free article.

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