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Lista de obras de Valérie Proulle

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

artículo científico publicado en 2017

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

artículo científico publicado en 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.

artículo científico publicado en 2016

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

artículo científico publicado el 15 de julio de 1997

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

artículo científico publicado en 2005

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.

artículo científico publicado en 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.

artículo científico publicado en 2000

Gene frequencies of human platelet antigens in the Tunisian population.

artículo científico publicado en 1999

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

artículo científico publicado en 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

artículo científico publicado en 2005

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

artículo científico publicado en 2001

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2018

Misdiagnosis of chronic thrombocytopenia in childhood.

artículo científico publicado en 2003

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

artículo científico publicado en 2011

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

artículo científico publicado en 2002

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

artículo científico publicado en 2014

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

artículo científico publicado en 2002

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

artículo científico publicado en 2001

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

artículo científico publicado en 2017

Risk factors for thrombosis in an african population.

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Spectrum of the mutations in Bernard-Soulier syndrome

artículo científico publicado en 2014

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

artículo científico publicado en 2008

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

artículo científico publicado en 2014

[Misdiagnosis of venous thrombosis in childhood]

artículo científico publicado en 2005

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

artículo científico publicado en 2011