van Dijk K - Search Results

1

Phenotype of severe hemophilia A and plasma levels of risk factors for thrombosis.

van Dijk K, van der Bom JG, Fischer K, de Groot PG, van den Berg HM. van Dijk K, et al. Among authors: van den berg hm, van der bom jg. J Thromb Haemost. 2007 May;5(5):1062-4. doi: 10.1111/j.1538-7836.2007.02447.x. Epub 2007 Feb 14. J Thromb Haemost. 2007. PMID: 17388802 Free article. No abstract available.

2

Do prothrombotic factors influence clinical phenotype of severe haemophilia? A review of the literature.

van Dijk K, van der Bom JG, Fischer K, Grobbee DE, van den Berg HM. van Dijk K, et al. Among authors: van den berg hm, van der bom jg. Thromb Haemost. 2004 Aug;92(2):305-10. doi: 10.1160/TH04-02-0112. Thromb Haemost. 2004. PMID: 15269826

3

Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed.

van Dijk K, Fischer K, van der Bom JG, Grobbee DE, van den Berg HM. van Dijk K, et al. Among authors: van den berg hm, van der bom jg. Haemophilia. 2005 Sep;11(5):438-43. doi: 10.1111/j.1365-2516.2005.01124.x. Haemophilia. 2005. PMID: 16128885

4

Factor VIII half-life and clinical phenotype of severe hemophilia A.

van Dijk K, van der Bom JG, Lenting PJ, de Groot PG, Mauser-Bunschoten EP, Roosendaal G, Grobbee DE, van den Berg HM. van Dijk K, et al. Among authors: van den berg hm, van der bom jg. Haematologica. 2005 Apr;90(4):494-8. Haematologica. 2005. PMID: 15820945

5

Can long-term prophylaxis for severe haemophilia be stopped in adulthood? Results from Denmark and the Netherlands.

van Dijk K, Fischer K, van der Bom JG, Scheibel E, Ingerslev J, van den Berg HM. van Dijk K, et al. Among authors: van den berg hm, van der bom jg. Br J Haematol. 2005 Jul;130(1):107-12. doi: 10.1111/j.1365-2141.2005.05546.x. Br J Haematol. 2005. PMID: 15982352 Free article.

6

Use of implantable venous access devices in children with severe hemophilia: benefits and burden.

Van Dijk K, Van Der Bom JG, Bax KN, Van Der Zee DC, Van Den Berg MH. Van Dijk K, et al. Among authors: van der zee dc, van der bom jg, van den berg mh. Haematologica. 2004 Feb;89(2):189-94. Haematologica. 2004. PMID: 15003894

7

Models for prediction of factor VIII half-life in severe haemophiliacs: distinct approaches for blood group O and non-O patients.

Fischer K, Pendu R, van Schooten CJ, van Dijk K, Denis CV, van den Berg HM, Lenting PJ. Fischer K, et al. Among authors: van dijk k, van den berg hm, van schooten cj. PLoS One. 2009 Aug 25;4(8):e6745. doi: 10.1371/journal.pone.0006745. PLoS One. 2009. PMID: 19707594 Free PMC article.

8

Successful low dose immune tolerance induction in severe haemophilia A with inhibitors below 40 Bethesda Units.

Ter Avest PC, Fischer K, Gouw SC, Van Dijk K, Mauser-Bunschoten EP. Ter Avest PC, et al. Among authors: van dijk k. Haemophilia. 2010 May;16(102):71-9. doi: 10.1111/j.1365-2516.2010.02225.x. Haemophilia. 2010. PMID: 20536988

9

Early versus late treatment of posthaemorrhagic ventricular dilatation: results of a retrospective study from five neonatal intensive care units in The Netherlands.

de Vries LS, Liem KD, van Dijk K, Smit BJ, Sie L, Rademaker KJ, Gavilanes AW; Dutch Working Group of Neonatal Neurology. de Vries LS, et al. Among authors: van dijk k. Acta Paediatr. 2002;91(2):212-7. doi: 10.1080/080352502317285234. Acta Paediatr. 2002. PMID: 11952011

10

The diagnosis and treatment of invasive aspergillosis in Dutch haematology units facing a rapidly increasing prevalence of azole-resistance. A nationwide survey and rationale for the DB-MSG 002 study protocol.

Schauwvlieghe AFAD, de Jonge N, van Dijk K, Verweij PE, Brüggemann RJ, Biemond BJ, Bart A, von dem Borne PA, Verbon A, van der Beek MT, Demandt AMP, Oudhuis GJ, Cornelissen JJ, van der Velden WJFM, Span LFR, Kampinga GA, Bruns AH, Vonk AG, Haas PA, Doorduijn JK, Rijnders BJA. Schauwvlieghe AFAD, et al. Among authors: van dijk k, van der velden wjfm, van der beek mt. Mycoses. 2018 Sep;61(9):656-664. doi: 10.1111/myc.12788. Epub 2018 Jul 13. Mycoses. 2018. PMID: 29687483

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