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LAD-1/variant syndrome is caused by mutations in FERMT3.
Kuijpers TW, van de Vijver E, Weterman MA, de Boer M, Tool AT, van den Berg TK, Moser M, Jakobs ME, Seeger K, Sanal O, Unal S, Cetin M, Roos D, Verhoeven AJ, Baas F. Kuijpers TW, et al. Among authors: van den berg tk, van de vijver e. Blood. 2009 May 7;113(19):4740-6. doi: 10.1182/blood-2008-10-182154. Epub 2008 Dec 8. Blood. 2009. PMID: 19064721 Free article.
A novel flow cytometry-based platelet aggregation assay.
De Cuyper IM, Meinders M, van de Vijver E, de Korte D, Porcelijn L, de Haas M, Eble JA, Seeger K, Rutella S, Pagliara D, Kuijpers TW, Verhoeven AJ, van den Berg TK, Gutiérrez L. De Cuyper IM, et al. Among authors: van den berg tk, van de vijver e. Blood. 2013 Mar 7;121(10):e70-80. doi: 10.1182/blood-2012-06-437723. Epub 2013 Jan 9. Blood. 2013. PMID: 23303822 Free article.
Leukocyte adhesion deficiencies.
van de Vijver E, van den Berg TK, Kuijpers TW. van de Vijver E, et al. Among authors: van den berg tk. Hematol Oncol Clin North Am. 2013 Feb;27(1):101-16, viii. doi: 10.1016/j.hoc.2012.10.001. Epub 2012 Nov 13. Hematol Oncol Clin North Am. 2013. PMID: 23351991 Review.
Human NLRP3 inflammasome activation is Nox1-4 independent.
van Bruggen R, Köker MY, Jansen M, van Houdt M, Roos D, Kuijpers TW, van den Berg TK. van Bruggen R, et al. Among authors: van houdt m, van den berg tk. Blood. 2010 Jul 1;115(26):5398-400. doi: 10.1182/blood-2009-10-250803. Epub 2010 Apr 20. Blood. 2010. PMID: 20407038 Free article.
Invasive fungal infection and impaired neutrophil killing in human CARD9 deficiency.
Drewniak A, Gazendam RP, Tool AT, van Houdt M, Jansen MH, van Hamme JL, van Leeuwen EM, Roos D, Scalais E, de Beaufort C, Janssen H, van den Berg TK, Kuijpers TW. Drewniak A, et al. Among authors: van houdt m, van den berg tk, van leeuwen em, van hamme jl. Blood. 2013 Mar 28;121(13):2385-92. doi: 10.1182/blood-2012-08-450551. Epub 2013 Jan 18. Blood. 2013. PMID: 23335372 Free article.
Defects in neutrophil granule mobilization and bactericidal activity in familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) syndrome caused by STXBP2/Munc18-2 mutations.
Zhao XW, Gazendam RP, Drewniak A, van Houdt M, Tool AT, van Hamme JL, Kustiawan I, Meijer AB, Janssen H, Russell DG, van de Corput L, Tesselaar K, Boelens JJ, Kuhnle I, Van Der Werff Ten Bosch J, Kuijpers TW, van den Berg TK. Zhao XW, et al. Among authors: van houdt m, van den berg tk, van der werff ten bosch j, van hamme jl, van de corput l. Blood. 2013 Jul 4;122(1):109-11. doi: 10.1182/blood-2013-03-494039. Epub 2013 May 17. Blood. 2013. PMID: 23687090 Free article.
183 results