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Aspirin in essential thrombocythemia: status quo and quo vadis.
Griesshammer M, Bangerter M, van Vliet HH, Michiels JJ. Griesshammer M, et al. Semin Thromb Hemost. 1997;23(4):371-7. doi: 10.1055/s-2007-996111. Semin Thromb Hemost. 1997. PMID: 9263354 Review.
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. 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
Transient neurologic and ocular manifestations in primary thrombocythemia.
Michiels JJ, Koudstaal PJ, Mulder AH, van Vliet HH. Michiels JJ, et al. Neurology. 1993 Jun;43(6):1107-10. doi: 10.1212/wnl.43.6.1107. Neurology. 1993. PMID: 8170552
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. Ann Hematol. 1994 Aug;69(2):81-4. doi: 10.1007/BF01698487. Ann Hematol. 1994. PMID: 8080884
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. 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.
[Intermittent thrombocytopenia as a manifestation of Von Willebrand's disease].
Gómez García EB, Brouwers GJ, Kappers-Klunne MC, Leebeek FW, van Vliet HH. Gómez García EB, et al. Ned Tijdschr Geneeskd. 2002 Jun 22;146(25):1192-5. Ned Tijdschr Geneeskd. 2002. PMID: 12109311 Dutch.
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