Van Wijk R - Search Results

1

Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.

Van Zwieten R, François JJ, Van Leeuwen K, Van Wesel AC, Van Bruggen R, Van Solinge WW, Roos D, Verhoeven AJ, Van Wijk R. Van Zwieten R, et al. Among authors: van leeuwen k, van bruggen r, van wesel ac, van wijk r, van solinge ww. Am J Hematol. 2013 Feb;88(2):159-60. doi: 10.1002/ajh.23363. Epub 2012 Dec 17. Am J Hematol. 2013. PMID: 23255290 Free article. No abstract available.

2

Five novel mutations in the gene for human blood coagulation factor V associated with type I factor V deficiency.

van Wijk R, Nieuwenhuis K, van den Berg M, Huizinga EG, van der Meijden BB, Kraaijenhagen RJ, van Solinge WW. van Wijk R, et al. Among authors: van den berg m, van solinge ww, van der meijden bb. Blood. 2001 Jul 15;98(2):358-67. doi: 10.1182/blood.v98.2.358. Blood. 2001. PMID: 11435304 Free article.

3

Nature of the fibrinogen Aalpha gene TaqI polymorphism.

Remijn JA, van Wijk R, de Groot PG, van Solinge WW. Remijn JA, et al. Among authors: van wijk r, van solinge ww. Thromb Haemost. 2001 Sep;86(3):935-6. Thromb Haemost. 2001. PMID: 11583334 No abstract available.

4

Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aalpha gene.

Vlietman JJ, Verhage J, Vos HL, van Wijk R, Remijn JA, van Solinge WW, Brus F. Vlietman JJ, et al. Among authors: van wijk r, van solinge ww. Br J Haematol. 2002 Oct;119(1):282-3. doi: 10.1046/j.1365-2141.2002.377910.x. Br J Haematol. 2002. PMID: 12358944 Free article. No abstract available.

5

[From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency].

de Vooght KM, van Wijk R, Nieuwenhuis HK, Ploos van Amstel JK, Rijksen G, van Solinge WW. de Vooght KM, et al. Among authors: van wijk r, van solinge ww. Ned Tijdschr Geneeskd. 2002 Sep 28;146(39):1828-31. Ned Tijdschr Geneeskd. 2002. PMID: 12382367 Dutch.

6

Disruption of a novel regulatory element in the erythroid-specific promoter of the human PKLR gene causes severe pyruvate kinase deficiency.

van Wijk R, van Solinge WW, Nerlov C, Beutler E, Gelbart T, Rijksen G, Nielsen FC. van Wijk R, et al. Among authors: van solinge ww. Blood. 2003 Feb 15;101(4):1596-602. doi: 10.1182/blood-2002-07-2321. Epub 2002 Sep 26. Blood. 2003. PMID: 12393511 Free article.

7

HK Utrecht: missense mutation in the active site of human hexokinase associated with hexokinase deficiency and severe nonspherocytic hemolytic anemia.

van Wijk R, Rijksen G, Huizinga EG, Nieuwenhuis HK, van Solinge WW. van Wijk R, et al. Among authors: van solinge ww. Blood. 2003 Jan 1;101(1):345-7. doi: 10.1182/blood-2002-06-1851. Epub 2002 Aug 8. Blood. 2003. PMID: 12393545 Free article.

8

Molecular basis of congenital afibrinogenaemia in a Dutch family.

Remijn JA, van Wijk R, Nieuwenhuis HK, de Groot PG, van Solinge WW. Remijn JA, et al. Among authors: van wijk r, van solinge ww. Blood Coagul Fibrinolysis. 2003 Apr;14(3):299-302. doi: 10.1097/01.mbc.0000061285.28953.be. Blood Coagul Fibrinolysis. 2003. PMID: 12695755

9

Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase.

van Wijk R, Huizinga EG, Prins I, Kors A, Rijksen G, Bierings M, van Solinge WW. van Wijk R, et al. Among authors: van solinge ww. Blood Cells Mol Dis. 2004 Jan-Feb;32(1):112-7. doi: 10.1016/j.bcmd.2003.10.006. Blood Cells Mol Dis. 2004. PMID: 14757424

10

Pyruvate kinase regulatory element 1 (PKR-RE1) mediates hexokinase gene expression in K562 cells.

de Vooght KM, van Wijk R, van Oirschot BA, Rijksen G, van Solinge WW. de Vooght KM, et al. Among authors: van oirschot ba, van wijk r, van solinge ww. Blood Cells Mol Dis. 2005 Mar-Apr;34(2):186-90. doi: 10.1016/j.bcmd.2004.10.002. Blood Cells Mol Dis. 2005. PMID: 15727904

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