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- 2008
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Mark
Genetic aspects and research development in haemostasis
(
- Contribution to journal › Article
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Mark
Being a carrier of haemophilia - how does it influence quality of life?
2008) XXVIIIth International Congress of the World Federation of Hemophilia, 2008 In Haemophilia 14(s2). p.152-153(
- Contribution to journal › Published meeting abstract
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Mark
Prophylaxis in von Willebrand disease.
(
- Contribution to journal › Article
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Mark
Isolation of bacteria-containing phagosomes by magnetic selection.
(
- Contribution to journal › Article
-
Mark
Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families?
(
- Contribution to journal › Article
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Mark
Intracranial haemorrhage in haemophilia A and B.
(
- Contribution to journal › Scientific review
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Mark
Towards a better understanding and new therapeutics of osteopetrosis.
(
- 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.
(
- Contribution to journal › Article
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Mark
Advances in understanding pathogenic mechanisms of thrombophilic disorders.
(
- Contribution to journal › Article
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Mark
Haemophilia in the first years of life.
(
- Contribution to journal › Article