van Vliet HH - Search Results

1

Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.

Michiels JJ, van der Luit L, van Vliet HH, Jochmans K, Lissens W. Michiels JJ, et al. Among authors: van vliet hh, van der luit l. Thromb Res. 1995 May 1;78(3):251-4. doi: 10.1016/0049-3848(95)90875-g. Thromb Res. 1995. PMID: 7631305 No abstract available.

2

Hereditary antithrombin III deficiency and venous thrombosis.

Michiels JJ, Van Vliet HH. Michiels JJ, et al. Among authors: van vliet hh. Neth J Med. 1984;27(6):226-32. Neth J Med. 1984. PMID: 6379481 Review. No abstract available.

3

Platelet consumption in thrombocythemia complicated by erythromelalgia: reversal by aspirin.

van Genderen PJ, Michiels JJ, van Strik R, Lindemans J, van Vliet HH. van Genderen PJ, et al. Among authors: van vliet hh, van strik r. Thromb Haemost. 1995 Feb;73(2):210-4. Thromb Haemost. 1995. PMID: 7792731

4

Erythromelalgia and arterial thrombophilia in thrombocythemia.

Michiels JJ, Van Genderen PJ, Van Vliet HH. Michiels JJ, et al. Among authors: van vliet hh, van genderen pj. Ann N Y Acad Sci. 1994 Apr 18;714:318-21. doi: 10.1111/j.1749-6632.1994.tb12067.x. Ann N Y Acad Sci. 1994. PMID: 8017789 No abstract available.

5

Phenotyping and genotyping of coagulation factor V Leiden.

Engel H, Zwang L, van Vliet HH, Michiels JJ, Stibbe J, Lindemans J. Engel H, et al. Among authors: van vliet hh. Thromb Haemost. 1996 Feb;75(2):267-9. Thromb Haemost. 1996. PMID: 8815574

6

Erythromelalgia in essential thrombocythemia is characterized by platelet activation and endothelial cell damage but not by thrombin generation.

van Genderen PJ, Lucas IS, van Strik R, Vuzevski VD, Prins FJ, van Vliet HH, Michiels JJ. van Genderen PJ, et al. Among authors: van vliet hh, van strik r. Thromb Haemost. 1996 Sep;76(3):333-8. Thromb Haemost. 1996. PMID: 8883266

7

Acquired von Willebrand disease in monoclonal gammapathies: effectiveness of high-dose intravenous gamma globulin.

Michiels JJ, van Vliet HH. Michiels JJ, et al. Among authors: van vliet hh. Clin Appl Thromb Hemost. 1999 Jul;5(3):152-7. doi: 10.1177/107602969900500302. Clin Appl Thromb Hemost. 1999. PMID: 10726000 Free article.

8

PFA-100 monitoring of von Willebrand factor (VWF) responses to desmopressin (DDAVP) and factor VIII/VWF concentrate substitution in von Willebrand disease type 1 and 2.

van Vliet HH, Kappers-Klunne MC, Leebeek FW, Michiels JJ. van Vliet HH, et al. Thromb Haemost. 2008 Sep;100(3):462-8. Thromb Haemost. 2008. PMID: 18766263

9

Heparin-induced thrombocytopenia and thrombosis: a potential fatal complication in a routine treatment.

Boon DM, Kappers-Klunne MC, Michiels JJ, Stibbe J, van Vliet HH. Boon DM, et al. Among authors: van vliet hh. Neth J Med. 1995 Mar;46(3):146-52. doi: 10.1016/0300-2977(94)00064-g. Neth J Med. 1995. PMID: 7731489

10

Acquired von Willebrand disease as a cause of recurrent mucocutaneous bleeding in primary thrombocythemia: relationship with platelet count.

van Genderen PJ, Michiels JJ, van der Poel-van de Luytgaarde SC, van Vliet HH. van Genderen PJ, et al. Among authors: van der poel van de luytgaarde sc, van vliet hh. Ann Hematol. 1994 Aug;69(2):81-4. doi: 10.1007/BF01698487. Ann Hematol. 1994. PMID: 8080884 Free article.

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