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Publications by W F Bahou
The Molecular Defect in Type IIB Von Willebrand Disease. Identification of Four Potential Missense Mutations Within the Putative GpIb Binding Domain.
Journal of Clinical Investigation
Medicine
Related publications
Functional Analysis of a Type IIB Von Willebrand Disease Missense Mutation: Increased Binding of Large Von Willebrand Factor Multimers to Platelets.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Molecular Basis of Von Willebrand Disease Type IIB. Candidate Mutations Cluster in One Disulfide Loop Between Proposed Platelet Glycoprotein Ib Binding Sequences.
Journal of Clinical Investigation
Medicine
Mutations of Von Willebrand Factor Gene in Families With Von Willebrand Disease in the Aland Islands.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Platelet GpIb Binding to Von Willebrand Factor Under Fluid Shear: Contributions of the D'd3-Domain, A1-Domain Flanking Peptide and O-Linked Glycans
Journal of the American Heart Association
Cardiovascular Medicine
Cardiology
Von Willebrand Disease Type 3
Critical Von Willebrand Factor A1 Domain Residues Influence Type VI Collagen Binding
Journal of Thrombosis and Haemostasis
Medicine
Hematology
The Molecular Characterization of Von Willebrand Disease: Good in Parts
British Journal of Haematology
Hematology
Identification and Functional Analysis of a Novel Von Willebrand Factor Mutation in a Family With Type 2A Von Willebrand Disease
PLoS ONE
Multidisciplinary
Identification and Characterisation of Mutations Associated With Von Willebrand Disease in a Turkish Patient Cohort
Thrombosis and Haemostasis
Hematology
