Author details

Full Name

Delphine Borgel

Affiliation

ORCID

Career Start Year

1982

Papers

111

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37542768	Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.		2023
37207862	MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.	J Thromb Haemost	2023
37193126	Hemostatic defects in congenital disorders of glycosylation.		2023
35060654	Emicizumab does not interfere with the activated clotting time.	Haemophilia	2022
35445541	Antithrombotic potential of a single-domain antibody enhancing the activated protein C-cofactor activity of protein S.	Journal of Thrombosis and Haemostasis	2022
35945284	Author Correction: Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome.	Nat Med	2022
35871859	Antithrombin supplementation for prevention of vascular thrombosis after pediatric liver transplantation.	Journal of Pediatric Surgery	2022
35717947	N-Glycosylation Deficiency Reduces the Activation of Protein C and Disrupts Endothelial Barrier Integrity.	Thromb Haemost	2022
34134169	The Proteolytic Inactivation of Protein Z-Dependent Protease Inhibitor by Neutrophil Elastase Might Promote the Procoagulant Activity of Neutrophil Extracellular Traps in Sepsis.	Thrombosis and Haemostasis	2022
35174614	How can the design of therapeutic SERPINs be improved?	Journal of Thrombosis and Haemostasis	2022
35075289	Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome.	Nat Med	2022
33038796	Cyclic bridged analogs of isoCA-4: Design, synthesis and biological evaluation.	European Journal of Medicinal Chemistry	2021
34237187	A retrospective analysis of discordances between international normalized ratio (INR) self-testing and INR laboratory testing in a pediatric patient population.	International Journal of Laboratory Hematology	2021
33964207	A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.	Am J Hum Genet	2021
34011136	Non-inhibitory antibodies inducing increased emicizumab clearance in a severe haemophilia A inhibitor patient.	Haematologica	2021
33475155	Assessing bleeding risk in 18 children with Osteogenesis imperfecta.	British Journal of Haematology	2021
34004050	Reappearance of inhibitor in a tolerized patient with severe haemophilia A during FVIII-free emicizumab therapy.	Haemophilia	2021
34049308	Endothelial Dysfunction as a Component of Severe Acute Respiratory Syndrome Coronavirus 2-Related Multisystem Inflammatory Syndrome in Children With Shock.	Critical Care Medicine	2021
33512067	TRPV4 channel activation induces the transition of venous and arterial endothelial cells toward a pro-inflammatory phenotype.	Physiological Reports	2021
34189397	Anti-inflammatory Activity of the Protein Z-Dependent Protease Inhibitor.		2021
34245688	SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy.	Clin Chim Acta	2021
33134771	Measuring beta-galactose exposure on platelets: Standardization and healthy reference values.	Research and Practice in Thrombosis and Haemostasis	2020
32266963	Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation.	J Inherit Metab Dis	2020
31694064	Clinical variability and probable founder effect in oculocutaneous albinism type 7.	Clinical Genetics	2020
33490121	Serpins in Hemostasis as Therapeutic Targets for Bleeding or Thrombotic Disorders.	Frontiers in Cardiovascular Medicine	2020
33098580	Long term outcome of MPI-CDG patients on D-mannose therapy.	Journal of Inherited Metabolic Disease	2020
33036649	Factor XII in PMM2-CDG patients: role of N-glycosylation in the secretion and function of the first element of the contact pathway.	Orphanet Journal of Rare Diseases	2020
32588751	NAADP/SERCA3-Dependent Ca Stores Pathway Specifically Controls Early Autocrine ADP Secretion Potentiating Platelet Activation.	Circulation Research	2020
30943907	Fulminant arterial vasculitis as an unusual complication of disseminated staphylococcal disease due to the emerging CC1 methicillin-susceptible Staphylococcus aureus clone: a case report.	BMC Infectious Diseases	2019
31736432	Inflammation in deep vein thrombosis: a therapeutic target?	Hematology	2019
30395857	Impact of Heparin- or Nonheparin-Coated Circuits on Platelet Function in Pediatric Cardiac Surgery.	Ann Thorac Surg	2019
30293989	Long-term follow-up in PMM2-CDG: are we ready to start treatment trials?	Genet Med	2019
30819911	Relevance of platelet desialylation and thrombocytopenia in type 2B von Willebrand disease: preclinical and clinical evidence.	Haematologica	2019
31271700	Elevated thrombin generation in patients with congenital disorder of glycosylation and combined coagulation factor deficiencies.	Journal of Thrombosis and Haemostasis	2019
30740725	International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up.	J Inherit Metab Dis	2019
29630665	An ADAM-10 dependent EPCR shedding links meningococcal interaction with endothelial cells to purpura fulminans.	PLoS Pathogens	2018
30115659	A mutation in the gene coding for the sialic acid transporter SLC35A1 is required for platelet life span but not proplatelet formation.	Haematologica	2018
30446499	TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology.	EMBO Molecular Medicine	2018
30256422	Pharmacokinetics of Enoxaparin After Renal Transplantation in Pediatric Patients.	Journal of Clinical Pharmacology	2018
30004697	Design and Synthesis of Tubulin and Histone Deacetylase Inhibitor Based on iso-Combretastatin A-4.	Journal of Medicinal Chemistry	2018
29519941	Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability.	Arteriosclerosis, Thrombosis, and Vascular Biology	2018
29202409	A fluorine scan of a tubulin polymerization inhibitor isocombretastatin A-4: Design, synthesis, molecular modelling, and biological evaluation.	Eur J Med Chem	2018
29363751	Inactivated antithombin as anticoagulant reversal in a rat model of cardiopulmonary bypass: a potent and potentially safer alternative to protamine.	British Journal of Haematology	2018
29800795	Endothelial cell surface limits coagulation without modulating the antithrombin potency.	Thrombosis Research	2018
27786339	Antithrombin is not protective against renal ischaemia-reperfusion injury.	Thrombosis and Haemostasis	2017
28954837	Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature.	J Med Genet	2017
28334263	Pathogenesis of meningococcal purpura fulminans.	Pathogens and Disease	2017
29043982	Preanalytical influence of pneumatic tube delivery system on results of routine biochemistry and haematology analysis.		2017
30046680	Platelet-mapping assay for monitoring antiplatelet therapy during mechanical circulatory support in children: A retrospective observational study.	Research and Practice in Thrombosis and Haemostasis	2017
29222696	Thrombomodulin favors leukocyte microvesicle fibrinolytic activity, reduces NETosis and prevents septic shock-induced coagulopathy in rats.	Annals of Intensive Care	2017