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- 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).
(
- Contribution to journal › Article
-
Mark
Predictors of deterioration of lung function in cystic fibrosis.
(
- Contribution to journal › Article
- 1997
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Mark
Bernard-Soulier syndrome Karlstad : Trp 498-->Stop mutation resulting in a truncated glycoprotein Ib alpha that contains part of the transmembranous domain
(
- Contribution to journal › Article
-
Mark
von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura
(
- Contribution to journal › Article
- 1996
-
Mark
Increased platelet retention in familial recurrent thrombotic thrombocytopenic purpura
(
- Contribution to journal › Article
- 1992
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Mark
Cerebral infarction in a girl who developed anticardiolipin syndrome after acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 1990
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Mark
Platelet surface-bound IgG and platelet-specific IgG in plasma in childhood thrombocytopenia
(
- Contribution to journal › Article
- 1986
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Mark
Platelet-associated IgG in childhood idiopathic thrombocytopenic purpura : measurements on intact and solubilized platelets and after gammaglobulin treatment
(
- Contribution to journal › Article
- 1985
-
Mark
Polymorphism of normal factor IX detected by mouse monoclonal antibodies
1985) In Proceedings of the National Academy of Sciences of the United States of America 82(11). p.3839-3843(
- Contribution to journal › Article
- 1983
-
Mark
Detection of factor IX inhibitors by immunoradiometric assay
(
- Contribution to journal › Article