Christina Isaksson (Former)
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- 2008
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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.
(
- Contribution to journal › Article
- 2002
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Mark
Von Willebrand's disease caused by compound heterozygosity for a substitution mutation (T1156M) in the D3 domain of the von Willebrand factor and a stop mutation (Q2470X).
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- Contribution to journal › Article
- 1998
-
Mark
Apoptosis of renal cortical cells in the hemolytic-uremic syndrome: : In vivo and in vitro studies
(
- Contribution to journal › Article