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Citation: W. Xu et al., Human endothelial cells maintain anti-aggregatory activity for platelets during apoptosis, THROMB HAEM, 85(5), 2001, pp. 915-923
Citation: Ej. Favaloro, Detection of von Willebrand disorder and identification of qualitative vonWillebrand factor defects - Direct comparison of commercial ELISA-based von Willebrand factor activity options, AM J CLIN P, 114(4), 2000, pp. 608-618
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Citation: Da. Facey et al., Type 2B von Willebrand's disease in thirteen individuals from five unrelated Australian families: Phenotype and genotype correlations, AM J HEMAT, 63(4), 2000, pp. 197-199
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Citation: Ej. Favaloro et al., Discrimination of von Willebrands disease (VWD) subtypes: Direct comparison of von Willebrand factor : collagen binding assay (VWF : CBA) with monoclonal antibody (MAB) based VWF-capture systems, THROMB HAEM, 84(4), 2000, pp. 541-547
Citation: Ej. Favaloro, Sulfatide-binding assay for von Willebrand factor: Detection of von Willebrand's disease without discrimination of vWD subtypes, THROMB RES, 98(2), 2000, pp. 213-219
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Citation: M. De Luca et al., Structure and function of the von Willebrand factor A1 domain: analysis with monoclonal antibodies reveals distinct binding sites involved in recognition of the platelet membrane glycoprotein Ib-IX-V complex and ristocetin-dependent activation, BLOOD, 95(1), 2000, pp. 164-172
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Citation: Ej. Favaloro et al., Laboratory testing, diagnosis, and management of von Willebrand disease - Current practice in Australasia, AM J CLIN P, 112(5), 1999, pp. 712-719
Citation: Ej. Favaloro et al., Functional activated protein C resistance assays: correlation with factor V DNA analysis is better with RVVT- than APTT-based assays, BR J BIOMED, 56(1), 1999, pp. 23-33
Citation: Ej. Favaloro et al., Use of a novel platelet function analyzer (PFA-100 (TM)) with high sensitivity to disturbances in von willebrand factor to screen for von Willebrand's disease and other disorders, AM J HEMAT, 62(3), 1999, pp. 165-174
Citation: Ms. Hertzberg et al., Mesenteric vein thrombosis secondary to combined protein C deficiency and double heterozygosity for factor V Leiden and prothrombin G20210A, AM J HEMAT, 62(3), 1999, pp. 199-200
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Citation: Ej. Favaloro et al., Laboratory testing for von Willebrand's disease: an assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey, THROMB HAEM, 82(4), 1999, pp. 1276-1282
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Citation: O. Mirochnik et al., A novel Factor V null mutation at Arg 506 causes a false positive Factor VLeiden result, THROMB HAEM, 82(3), 1999, pp. 1198-1199
Citation: Ej. Favaloro, Laboratory assessment as a critical component of the appropriate diagnosisand sub-classification of von Willebrand's disease, BLOOD REV, 13(4), 1999, pp. 185-204
Citation: Ej. Favaloro et al., Clinical utility of anticardiolipin antibody assays: High inter-laboratoryvariation and limited consensus by participants of external quality assurance programs signals a cautious approach, PATHOLOGY, 31(2), 1999, pp. 142-147
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Citation: Ma. Allman-farinelli et al., Comparison of the effects of two low fat diets with different alpha-linolenic : linoleic acid ratios on coagulation and fibrinolysis, ATHEROSCLER, 142(1), 1999, pp. 159-168
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Citation: Da. Facey et al., Identification and characterization of a novel mutation in von Willebrand factor causing type 2B von Willebrand's disease, BR J HAEM, 105(2), 1999, pp. 538-541
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