List of works - Valérie Proulle

A Novel Single-Domain Antibody Against von Willebrand Factor A1 Domain Resolves Leukocyte Recruitment and Vascular Leakage During Inflammation-Brief Report.

scientific article published on 22 June 2017

A factor VIII–nanobody fusion protein forming an ultrastable complex with VWF: effect on clearance and antibody formation

scientific article published on 31 July 2018

A novel missense mutation in a leucine-rich repeat of GPIbα in a Bernard-Soulier variant reduces shear-dependent adherence on von Willebrand factor

scientific article published on 01 July 2019

A specific plasminogen activator inhibitor-1 antagonist derived from inactivated urokinase.

scientific article

A three amino acid deletion in glycoprotein IIIa is responsible for type I Glanzmann's thrombasthenia: importance of residues Ile325Pro326Gly327 for beta3 integrin subunit association ⬇️

scientific article published on July 15, 1997

Circulating microparticles are elevated in haemophiliacs and non-haemophilic individuals aged <18 years.

scientific article

Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

scientific article published on 17 January 2019

Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution.

scientific article published in July 2006

FVIII dosages in persons with haemophilia A treated with extended half-life products: From local biology to optimized patient management

scientific article published on 17 June 2019

GPIaIIa as a candidate target for anti-platelet autoantibody occurring during valproate therapy and associated with peroperative bleeding.

scientific article published in January 2000

Gene frequencies of human platelet antigens in the Tunisian population.

scientific article

Heparin-induced thrombocytopenia: successful biological and clinical management with lepirudin despite severe renal impairment

scientific article published on 12 January 2011

Identification of genes involved in Ca2+ ionophore A23187-mediated apoptosis and demonstration of a high susceptibility for transcriptional repression of cell cycle genes in B lymphoblasts from a patient with Scott syndrome

scientific article

Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate

scientific article published on 01 November 2001

LDL receptor-related protein 1 contributes to the clearance of the activated factor VII-antithrombin complex.

scientific article published on 10 September 2016

LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B.

scientific article

Macrophage scavenger-receptor SR-AI contributes to the clearance of von Willebrand factor

scientific article published on 11 January 2018

Misdiagnosis of chronic thrombocytopenia in childhood.

scientific article

Multiplate whole blood impedance aggregometry: a new tool for von Willebrand disease.

scientific article

Myocardial infarction occurring in a case of acquired haemophilia during the treatment course with recombinant activated factor VII

scientific article published on 01 October 2002

Platelets are required for enhanced activation of the endothelium and fibrinogen in a mouse thrombosis model of APS.

scientific article

Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti-glycoprotein IIb-IIIa antibodies

scientific article published on 01 December 2002

Protein A sepharose immunoadsorption: immunological and haemostatic effects in two cases of acquired haemophilia.

scientific article

Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis

scientific article published on 15 June 2017

Risk factors for thrombosis in an african population.

scientific article

Soluble Siglec-5 associates to PSGL-1 and displays anti-inflammatory activity

scientific article

Spectrum of the mutations in Bernard-Soulier syndrome

scientific article

Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome).

scientific article

Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacity

scientific article published on 01 February 2003

Underestimation of unfractionated heparin therapy assessment due to platelet activation when using partial-draw (pediatric) citrate collection tubes

scientific article published on 27 August 2014

[Misdiagnosis of venous thrombosis in childhood]

scientific article published on 01 February 2005

β₂-Glycoprotein-1 autoantibodies from patients with antiphospholipid syndrome are sufficient to potentiate arterial thrombus formation in a mouse model.

scientific article

List of works by Valérie Proulle

A Novel Single-Domain Antibody Against von Willebrand Factor A1 Domain Resolves Leukocyte Recruitment and Vascular Leakage During Inflammation-Brief Report.

A factor VIII–nanobody fusion protein forming an ultrastable complex with VWF: effect on clearance and antibody formation

A novel missense mutation in a leucine-rich repeat of GPIbα in a Bernard-Soulier variant reduces shear-dependent adherence on von Willebrand factor

A specific plasminogen activator inhibitor-1 antagonist derived from inactivated urokinase.

A three amino acid deletion in glycoprotein IIIa is responsible for type I Glanzmann's thrombasthenia: importance of residues Ile325Pro326Gly327 for beta3 integrin subunit association ⬇️

Circulating microparticles are elevated in haemophiliacs and non-haemophilic individuals aged <18 years.

Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution.

FVIII dosages in persons with haemophilia A treated with extended half-life products: From local biology to optimized patient management

GPIaIIa as a candidate target for anti-platelet autoantibody occurring during valproate therapy and associated with peroperative bleeding.

Gene frequencies of human platelet antigens in the Tunisian population.

Heparin-induced thrombocytopenia: successful biological and clinical management with lepirudin despite severe renal impairment

Identification of genes involved in Ca2+ ionophore A23187-mediated apoptosis and demonstration of a high susceptibility for transcriptional repression of cell cycle genes in B lymphoblasts from a patient with Scott syndrome

Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate

LDL receptor-related protein 1 contributes to the clearance of the activated factor VII-antithrombin complex.

LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B.

Macrophage scavenger-receptor SR-AI contributes to the clearance of von Willebrand factor

Misdiagnosis of chronic thrombocytopenia in childhood.

Multiplate whole blood impedance aggregometry: a new tool for von Willebrand disease.

Myocardial infarction occurring in a case of acquired haemophilia during the treatment course with recombinant activated factor VII

Platelets are required for enhanced activation of the endothelium and fibrinogen in a mouse thrombosis model of APS.

Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti-glycoprotein IIb-IIIa antibodies

Protein A sepharose immunoadsorption: immunological and haemostatic effects in two cases of acquired haemophilia.

Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis

Risk factors for thrombosis in an african population.

Soluble Siglec-5 associates to PSGL-1 and displays anti-inflammatory activity

Spectrum of the mutations in Bernard-Soulier syndrome

Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome).

Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacity

Underestimation of unfractionated heparin therapy assessment due to platelet activation when using partial-draw (pediatric) citrate collection tubes

[Misdiagnosis of venous thrombosis in childhood]

β₂-Glycoprotein-1 autoantibodies from patients with antiphospholipid syndrome are sufficient to potentiate arterial thrombus formation in a mouse model.