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Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide.
Hilbert L, Nurden P, Caron C, Nurden AT, Goudemand J, Meyer D, Fressinaud E, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease. Hilbert L, et al. Among authors: nurden p, nurden at. Thromb Haemost. 2006 Sep;96(3):290-4. doi: 10.1160/TH06-03-0157. Thromb Haemost. 2006. PMID: 16953269
Delayed immunologic thrombocytopenia induced by abciximab.
Nurden P, Clofent-Sanchez G, Jais C, Bermejo E, Leroux L, Coste P, Nurden AT. Nurden P, et al. Among authors: nurden at. Thromb Haemost. 2004 Oct;92(4):820-8. doi: 10.1160/TH04-04-0237. Thromb Haemost. 2004. PMID: 15467914
Phenotypic heterogeneity in the Gray platelet syndrome extends to the expression of TREM family member, TLT-1.
Nurden AT, Nurden P, Bermejo E, Combrié R, McVicar DW, Washington AV. Nurden AT, et al. Among authors: nurden p. Thromb Haemost. 2008 Jul;100(1):45-51. doi: 10.1160/TH08-02-0067. Thromb Haemost. 2008. PMID: 18612537 Free PMC article.
Usual levels of JAM-C and claudin-5, also members of the immunoglobulin receptor family, were detected in platelets of both patients. In contrast, P-selectin was markedly decreased for patient 1 but not patient 2. Two metalloproteases, MMP-2 and MMP-9 were normally present …
Usual levels of JAM-C and claudin-5, also members of the immunoglobulin receptor family, were detected in platelets of both patients. In con …
217 results