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- 2008
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Mark
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation.
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- Contribution to journal › Article
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Mark
A proposed plan for the management of adult sibling donors.
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- Contribution to journal › Article
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Mark
Inhibitor development.
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- Contribution to journal › Article
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Mark
Signaling pathways governing stem cell fate.
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- Contribution to journal › Scientific review
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Mark
N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets.
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- Contribution to journal › Article
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Mark
Advances in understanding pathogenic mechanisms of thrombophilic disorders.
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- Contribution to journal › Article
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Mark
Haemophilia in the first years of life.
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- Contribution to journal › Article
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Mark
The tetraspanin CD63 is involved in granule targeting of neutrophil elastase.
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- Contribution to journal › Article
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Mark
Early days of APC resistance and FV Leiden.
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- Contribution to journal › Article
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Mark
Protecting the joints of mice and men.
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- Contribution to journal › Article