Laboratory diagnosis and molecular basis of mild von Willebrand disease type 1.
Michiels, Jan Jacques
Laboratory diagnosis and molecular basis of mild von Willebrand disease type 1. [electronic resource] - Acta haematologica 2009 - 85-97 p. digital
Publication Type: Journal Article; Review
1421-9662
10.1159/000214847 doi
ABO Blood-Group System--genetics
Bleeding Time
Codon, Nonsense
Deamino Arginine Vasopressin--administration & dosage
Dose-Response Relationship, Drug
Genes, Dominant
Genes, Recessive
Genotype
Humans
Models, Molecular
Mutation, Missense
Platelet Aggregation--drug effects
Protein Structure, Quaternary
Protein Structure, Tertiary
Ristocetin--pharmacology
von Willebrand Diseases--classification
von Willebrand Factor--analysis
Laboratory diagnosis and molecular basis of mild von Willebrand disease type 1. [electronic resource] - Acta haematologica 2009 - 85-97 p. digital
Publication Type: Journal Article; Review
1421-9662
10.1159/000214847 doi
ABO Blood-Group System--genetics
Bleeding Time
Codon, Nonsense
Deamino Arginine Vasopressin--administration & dosage
Dose-Response Relationship, Drug
Genes, Dominant
Genes, Recessive
Genotype
Humans
Models, Molecular
Mutation, Missense
Platelet Aggregation--drug effects
Protein Structure, Quaternary
Protein Structure, Tertiary
Ristocetin--pharmacology
von Willebrand Diseases--classification
von Willebrand Factor--analysis