Michiels JJ - Search Results

1

Excessive prolongation of the bleeding time by aspirin in essential thrombocythemia is related to a decrease of large von Willebrand factor multimers in plasma.

van Genderen PJ, van Vliet HH, Prins FJ, van de Moesdijk D, van Strik R, Zijlstra FJ, Budde U, Michiels JJ. van Genderen PJ, et al. Among authors: michiels jj. Ann Hematol. 1997 Nov-Dec;75(5-6):215-20. doi: 10.1007/s002770050345. Ann Hematol. 1997. PMID: 9433378

2

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: michiels jj. Thromb Haemost. 1995 Feb;73(2):210-4. Thromb Haemost. 1995. PMID: 7792731

3

Acquired von Willebrand disease caused by an autoantibody selectively inhibiting the binding of von Willebrand factor to collagen.

van Genderen PJ, Vink T, Michiels JJ, van 't Veer MB, Sixma JJ, van Vliet HH. van Genderen PJ, et al. Among authors: michiels jj. Blood. 1994 Nov 15;84(10):3378-84. Blood. 1994. PMID: 7949092 Free article.

4

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: michiels jj. Ann Hematol. 1994 Aug;69(2):81-4. doi: 10.1007/BF01698487. Ann Hematol. 1994. PMID: 8080884 Free article.

5

Primary thrombocythemia: diagnosis, clinical manifestations and management.

van Genderen PJ, Michiels JJ. van Genderen PJ, et al. Among authors: michiels jj. Ann Hematol. 1993 Aug;67(2):57-62. doi: 10.1007/BF01788127. Ann Hematol. 1993. PMID: 8347730 Review. No abstract available.

6

The reduction of large von Willebrand factor multimers in plasma in essential thrombocythaemia is related to the platelet count.

van Genderen PJ, Budde U, Michiels JJ, van Strik R, van Vliet HH. van Genderen PJ, et al. Among authors: michiels jj. Br J Haematol. 1996 Jun;93(4):962-5. doi: 10.1046/j.1365-2141.1996.d01-1729.x. Br J Haematol. 1996. PMID: 8703834

7

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: michiels jj. Thromb Haemost. 1996 Sep;76(3):333-8. Thromb Haemost. 1996. PMID: 8883266

8

Erythromelalgic, thrombotic and hemorrhagic manifestations in 50 cases of thrombocythemia.

Michiels JJ, van Genderen PJ, Lindemans J, van Vliet HH. Michiels JJ, et al. Leuk Lymphoma. 1996 Sep;22 Suppl 1:47-56. doi: 10.3109/10428199609074360. Leuk Lymphoma. 1996. PMID: 8951772 Review.

9

Bleeding time and platelet function in essential thrombocythemia and other myeloproliferative syndromes.

Finazzi G, Budde U, Michiels JJ. Finazzi G, et al. Among authors: michiels jj. Leuk Lymphoma. 1996 Sep;22 Suppl 1:71-8. doi: 10.3109/10428199609074363. Leuk Lymphoma. 1996. PMID: 8951775 Review.

10

Acquired von Willebrand disease in myeloproliferative disorders.

van Genderen PJ, Leenknegt H, Michiels JJ, Budde U. van Genderen PJ, et al. Among authors: michiels jj. Leuk Lymphoma. 1996 Sep;22 Suppl 1:79-82. doi: 10.3109/10428199609074364. Leuk Lymphoma. 1996. PMID: 8951776 Review.

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