de Haas M - Search Results

1

Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B.

Breunis WB, van Mirre E, Geissler J, Laddach N, Wolbink G, van der Schoot E, de Haas M, de Boer M, Roos D, Kuijpers TW. Breunis WB, et al. Among authors: de haas m, de boer m. Hum Mutat. 2009 May;30(5):E640-50. doi: 10.1002/humu.20997. Hum Mutat. 2009. PMID: 19309690

2

Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura.

Breunis WB, van Mirre E, Bruin M, Geissler J, de Boer M, Peters M, Roos D, de Haas M, Koene HR, Kuijpers TW. Breunis WB, et al. Among authors: de haas m, de boer m. Blood. 2008 Feb 1;111(3):1029-38. doi: 10.1182/blood-2007-03-079913. Epub 2007 Sep 7. Blood. 2008. PMID: 17827395 Free article.

3

Genetic Variation in Low-To-Medium-Affinity Fcγ Receptors: Functional Consequences, Disease Associations, and Opportunities for Personalized Medicine.

Nagelkerke SQ, Schmidt DE, de Haas M, Kuijpers TW. Nagelkerke SQ, et al. Among authors: de haas m. Front Immunol. 2019 Oct 3;10:2237. doi: 10.3389/fimmu.2019.02237. eCollection 2019. Front Immunol. 2019. PMID: 31632391 Free PMC article. Review.

4

The association and functional relevance of genetic variation in low-to-medium-affinity Fc-gamma receptors with clinical platelet transfusion refractoriness.

Nagelkerke SQ, Porcelijn L, Geissler J, Tanck MWT, Huiskes E, van Bruggen R, van den Berg TK, de Haas M, Kuijpers TW. Nagelkerke SQ, et al. Among authors: de haas m. J Thromb Haemost. 2020 Aug;18(8):2047-2053. doi: 10.1111/jth.14892. Epub 2020 Jun 25. J Thromb Haemost. 2020. PMID: 32588549 Free article.

5

Transient and chronic childhood immune thrombocytopenia are distinctly affected by Fc-γ receptor polymorphisms.

Schmidt DE, Heitink-Pollé KMJ, Laarhoven AG, Bruin MCA, Veldhuisen B, Nagelkerke SQ, Kuijpers TW, Porcelijn L, van der Schoot CE, Vidarsson G, de Haas M. Schmidt DE, et al. Among authors: de haas m. Blood Adv. 2019 Jul 9;3(13):2003-2012. doi: 10.1182/bloodadvances.2019000068. Blood Adv. 2019. PMID: 31270082 Free PMC article.

6

RhIg-prophylaxis is not influenced by FCGR2/3 polymorphisms involved in red blood cell clearance.

Stegmann TC, Veldhuisen B, Nagelkerke SQ, Winkelhorst D, Schonewille H, Verduin EP, Kuijpers TW, de Haas M, Vidarsson G, van der Schoot CE. Stegmann TC, et al. Among authors: de haas m. Blood. 2017 Feb 23;129(8):1045-1048. doi: 10.1182/blood-2016-05-716365. Epub 2017 Jan 12. Blood. 2017. PMID: 28082442 Free article. No abstract available.

7

Neutrophil antigens, from bench to bedside.

von dem Borne AE, de Haas M, Roos D, Homburg CH, van der Schoot CE. von dem Borne AE, et al. Among authors: de haas m. Immunol Invest. 1995 Jan-Feb;24(1-2):245-72. doi: 10.3109/08820139509062776. Immunol Invest. 1995. PMID: 7713586 Review. No abstract available.

8

NA-phenotype-dependent differences in neutrophil Fc gamma RIIIb expression cause differences in plasma levels of soluble Fc gamma RIII.

Koene HR, de Haas M, Kleijer M, Roos D, von dem Borne AE. Koene HR, et al. Among authors: de haas m. Br J Haematol. 1996 Apr;93(1):235-41. doi: 10.1046/j.1365-2141.1996.4971038.x. Br J Haematol. 1996. PMID: 8611467

9

The use of rhG-CSF in chronic autoimmune neutropenia: reversal of autoimmune phenomena, a case history.

Kuijpers TW, de Haas M, de Groot CJ, von dem Borne AE, Weening RS. Kuijpers TW, et al. Among authors: de haas m, de groot cj. Br J Haematol. 1996 Sep;94(3):464-9. doi: 10.1046/j.1365-2141.1996.d01-1823.x. Br J Haematol. 1996. PMID: 8790143

10

Fc gamma RIIIB gene duplication: evidence for presence and expression of three distinct Fc gamma RIIIB genes in NA(1+,2+)SH(+) individuals.

Koene HR, Kleijer M, Roos D, de Haas M, Von dem Borne AE. Koene HR, et al. Among authors: de haas m. Blood. 1998 Jan 15;91(2):673-9. Blood. 1998. PMID: 9427724 Free article.

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