Search Results - "Mac Gillavry, M.R."

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    Protein C and S and inflammation in sickle cell disease by Schnog, J.B., Mac Gillavry, M.R., van Zanten, A.P., Meijers, J.C.M., Rojer, R.A., Duits, A.J., ten Cate, H., Brandjes, D.P.M.

    Published in American journal of hematology (01-05-2004)
    “…Reduced activity of naturally occurring anticoagulants (NOAC) protein C and protein S may contribute to vaso‐occlusion in sickle cell disease (SCD). We studied…”
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    Journal Article
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    Low adjusted‐dose acenocoumarol therapy in sickle cell disease: A pilot study by Schnog, J.B., Kater, A.P., Mac Gillavry, M.R., Duits, A.J., Lard, L.R., van der Dijs, F.P.L., Brandjes, D.P.M., ten Cate, H., Statius van Eps, L.W., Rojer, R.A.

    Published in American journal of hematology (01-11-2001)
    “…Vasoocclusion is a continuous process in sickle cell disease (SCD) and accumulates to significant end organ damage, mostly irrespective of the occurrence of…”
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    Journal Article
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    No effect of acenocoumarol therapy on levels of endothelial activation markers in sickle cell disease by Schnog, J.B., Mac Gillavry, M.R., Rojer, R.A., Meijers, J.C.M., Fijnheer, R., ten Cate, H., Brandjes, D.P.M., Duits, A.J.

    Published in American journal of hematology (01-09-2002)
    “…Sickle cell patients are characterized by a chronic inflammatory and hypercoagulable state, depicted by elevated levels of pro‐inflammatory cytokines,…”
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    Journal Article