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Clinical value of early viscoelastometric point‐of‐care testing during postpartum hemorrhage for the prediction of severity of bleeding: A multicenter prospective cohort study in the Netherlands.
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- Acta Obstetricia et Gynecologica Scandinavica, 2021, v. 100, n. 9, p. 1656, doi. 10.1111/aogs.14172
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- Article
Lowering the increased intracellular pH of human‐induced pluripotent stem cell‐derived endothelial cells induces formation of mature Weibel‐Palade bodies.
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- Stem Cells Translational Medicine, 2020, v. 9, n. 7, p. 758, doi. 10.1002/sctm.19-0392
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- Article
The association between haemorrhage and markers of endothelial insufficiency and inflammation in patients with hypoproliferative thrombocytopenia: a cohort study.
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- British Journal of Haematology, 2020, v. 189, n. 1, p. 171, doi. 10.1111/bjh.16291
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- Article
Association of Timing of Plasma Transfusion With Adverse Maternal Outcomes in Women With Persistent Postpartum Hemorrhage.
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- JAMA Network Open, 2019, v. 2, n. 11, p. e1915628, doi. 10.1001/jamanetworkopen.2019.15628
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- Article
The inheritance and molecular genetics of von Willebrand's disease.
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- Haemophilia, 1995, v. 1, n. 2, p. 77, doi. 10.1111/j.1365-2516.1995.tb00045.x
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- Article
Efficacy of recombinant activated Factor VII in patients with massive uncontrolled bleeding: a retrospective observational analysis.
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- Transfusion, 2009, v. 49, n. 3, p. 570, doi. 10.1111/j.1537-2995.2008.02001.x
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- Article
The clinical impact of platelet refractoriness: correlation with bleeding and survival.
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- Transfusion, 2008, v. 48, n. 9, p. 1959, doi. 10.1111/j.1537-2995.2008.01799.x
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- Article
High factor VIII antigen levels increase the risk of venous thrombosis but are not associated with polymorphisms in the von Willebrand factor and factor VIII gene.
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- British Journal of Haematology, 2001, v. 115, n. 1, p. 156, doi. 10.1046/j.1365-2141.2001.03089.x
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- Article
Autosomal dominant type 1 von Willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effect.
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- British Journal of Haematology, 2000, v. 108, n. 4, p. 876, doi. 10.1046/j.1365-2141.2000.01944.x
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- Article
Atherothrombosis model by silencing of protein C in APOE*3-Leiden.CETP transgenic mice.
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- Journal of Thrombosis & Thrombolysis, 2021, v. 52, n. 3, p. 715, doi. 10.1007/s11239-021-02488-2
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- Article
The spectrum of neutralizing and non-neutralizing anti-FVIII antibodies in a nationwide cohort of 788 persons with hemophilia A.
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- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1355813
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- Article
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutation.
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- British Journal of Haematology, 2000, v. 108, n. 1, p. 188, doi. 10.1046/j.1365-2141.2000.01807.x
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- Article
A novel candidate mutation (Arg<sup>611</sup>→ His) in type I'platelet discordant'von Willebrand's disease with desmopressin-induced thrombocytopenia.
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- British Journal of Haematology, 1995, v. 89, n. 3, p. 656, doi. 10.1111/j.1365-2141.1995.tb08383.x
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- Article
Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40.
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- British Journal of Haematology, 1993, v. 84, n. 3, p. 533, doi. 10.1111/j.1365-2141.1993.tb03114.x
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- Article
ACQUIRED VON WILLEBRAND'S DISEASE DUE TO EXCESSIVE FIBRINOLYSIS.
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- British Journal of Haematology, 1992, v. 81, n. 4, p. 618, doi. 10.1111/j.1365-2141.1992.tb03005.x
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- Article
A patient with von Willebrand's disease characterized by a compound heterozygosity for a substitution of Arg by Gln in the putative factor-VIII-binding domain of von Willebrand factor (vWF) on one allele and very low levels of mRNA from the second vWF allele
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- British Journal of Haematology, 1992, v. 80, n. 3, p. 358, doi. 10.1111/j.1365-2141.1992.tb08145.x
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- Article