Inge Pareyn

Kortrijk, VLG, Belgium

Last Updated: 09/26/2026

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Found 24 publications

The mitochondrial deacetylase SIRT3 is nonessential for cyclophilin D-dependent procoagulant platelet formation in mice.

The mitochondrial deacetylase SIRT3 is nonessential for cyclophilin D-dependent procoagulant platelet formation in mice.

Journal: Platelets
Published: September 03, 2026

The effects of balanced crystalloid versus plasma on endothelial injury, systemic inflammation, and coagulation in experimental endotoxaemia: a randomised human volunteer study.

The effects of balanced crystalloid versus plasma on endothelial injury, systemic inflammation, and coagulation in experimental endotoxaemia: a randomised human volunteer study.

Journal: British journal of anaesthesia
Published: May 26, 2025

A novel p.C1130S mutation in a Finnish family with a complex phenotype of von Willebrand disease.

A novel p.C1130S mutation in a Finnish family with a complex phenotype of von Willebrand disease.

Journal: Haematologica
Published: May 07, 2025

Novel cryptic ADAMTS13 epitopes uncover a distinct open ADAMTS13 conformation in immune-mediated TTP.

Novel cryptic ADAMTS13 epitopes uncover a distinct open ADAMTS13 conformation in immune-mediated TTP.

Journal: Haematologica
Published: April 25, 2025

Unraveling antibody-induced structural dynamics in the ADAMTS13 CUB1-2 domains via HDX-MS.

Unraveling antibody-induced structural dynamics in the ADAMTS13 CUB1-2 domains via HDX-MS.

Journal: Blood advances
Published: September 27, 2024

ADAMTS13 inhibition to treat acquired von Willebrand syndrome during mechanical circulatory support device implantation.

ADAMTS13 inhibition to treat acquired von Willebrand syndrome during mechanical circulatory support device implantation.

Journal: Journal of thrombosis and haemostasis : JTH
Published: June 23, 2022

Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency.

Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency.

Journal: Thrombosis and haemostasis
Published: September 13, 2020

Antibodies that conformationally activate ADAMTS13 allosterically enhance metalloprotease domain function.

Antibodies that conformationally activate ADAMTS13 allosterically enhance metalloprotease domain function.

Journal: Blood advances
Published: December 20, 2019

Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura.

Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura.

Journal: Blood
Published: November 20, 2019

von Willebrand factor increases in experimental cerebral malaria but is not essential for late-stage pathogenesis in mice.

von Willebrand factor increases in experimental cerebral malaria but is not essential for late-stage pathogenesis in mice.

Journal: Journal of thrombosis and haemostasis : JTH
Published: October 31, 2019

Acquired von Willebrand syndrome in patients on long-term left ventricular assist device support: Results of a Belgian center.

Acquired von Willebrand syndrome in patients on long-term left ventricular assist device support: Results of a Belgian center.

Journal: Thrombosis research
Published: September 12, 2019

Anti-ADAMTS13 autoantibodies in immune-mediated thrombotic thrombocytopenic purpura do not hamper ELISA-based quantification of ADAMTS13 antigen.

Anti-ADAMTS13 autoantibodies in immune-mediated thrombotic thrombocytopenic purpura do not hamper ELISA-based quantification of ADAMTS13 antigen.

Journal: Journal of thrombosis and haemostasis : JTH
Published: September 10, 2019
Showing 1-12 of 24

Last Updated: 09/26/2026