Lars Holmberg
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- 2007
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Mark
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
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- Contribution to journal › Article
- 2006
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Mark
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor
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- Contribution to journal › Scientific review
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Mark
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD)
(
- Contribution to journal › Article
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Mark
Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
(
- Contribution to journal › Article
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Mark
Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.
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- Contribution to journal › Article
- 2005
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Mark
VWF-cleaving protease (ADAMTS13) in premature infants.
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- Contribution to journal › Article
- 2004
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Mark
Sorting of Von Willebrand factor to lysosome-related granules of haematopoietic cells
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- Contribution to journal › Article
- 2003
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Mark
Desmopressin (DDAVP) and factor VIII
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- Contribution to journal › Debate/Note/Editorial
- 2002
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Mark
Predictors of deterioration of lung function in cystic fibrosis.
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- Contribution to journal › Article
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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