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Evaluation of different diagnostic tools for detection of acquired von Willebrand syndrome in patients with polycythemia vera or essential thrombocythemia
2022 - Forschungsinformationssystem des UKE
Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS
2021 - Forschungsinformationssystem des UKE - frei zugänglich
Comparison of von Willebrand factor platelet-binding activity assays:ELISA overreads type 2B with loss of HMW multimers
2020 - Forschungsinformationssystem des UKE
Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease:Results from 3WINTERS-IPS, an international and collaborative cross-sectional study
2020 - Forschungsinformationssystem des UKE
Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation
2020 - Forschungsinformationssystem des UKE
Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations
2019 - Forschungsinformationssystem des UKE
Characterization of VWF gene conversions causing von Willebrand disease
2019 - Forschungsinformationssystem des UKE
Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging
2019 - Forschungsinformationssystem des UKE - frei zugänglich
Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany
2018 - Forschungsinformationssystem des UKE
Mutation G1629E Increases von Willebrand Factor Cleavage via a Cooperative Destabilization Mechanism
2017 - Forschungsinformationssystem des UKE
Von Willebrand factor regulates complement on endothelial cells
2016 - Forschungsinformationssystem des UKE
von Willebrand factor is dimerized by protein disulfide isomerase
2016 - Forschungsinformationssystem des UKE
Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias
2016 - Forschungsinformationssystem des UKE
Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers
2016 - Forschungsinformationssystem des UKE
Treatment of acquired von Willebrand syndrome in aortic stenosis with transcatheter aortic valve replacement
2015 - Forschungsinformationssystem des UKE
Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus
2014 - Forschungsinformationssystem des UKE - frei zugänglich
Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion
2014 - Forschungsinformationssystem des UKE
Correction of acquired von Willebrand syndrome by transcatheter aortic valve implantation
2014 - Forschungsinformationssystem des UKE
Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin
2014 - Forschungsinformationssystem des UKE
Inherited thrombotic thrombocytopenic purpura in children
2014 - Forschungsinformationssystem des UKE

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Evaluation of different diagnostic tools for detection of acquired von Willebrand syndrome in patients with polycythemia vera or essential thrombocythemia

Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS

Comparison of von Willebrand factor platelet-binding activity assays:ELISA overreads type 2B with loss of HMW multimers

Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease:Results from 3WINTERS-IPS, an international and collaborative cross-sectional study

Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation

Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

Characterization of VWF gene conversions causing von Willebrand disease

Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging

Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany

Mutation G1629E Increases von Willebrand Factor Cleavage via a Cooperative Destabilization Mechanism

Von Willebrand factor regulates complement on endothelial cells

von Willebrand factor is dimerized by protein disulfide isomerase

Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias

Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers

Treatment of acquired von Willebrand syndrome in aortic stenosis with transcatheter aortic valve replacement

Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus

Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion

Correction of acquired von Willebrand syndrome by transcatheter aortic valve implantation

Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin

Inherited thrombotic thrombocytopenic purpura in children