Christine Andreani-Biron
Montpellier, France
Last Updated: 09/26/2026
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Found 42 publications
Real-word evidence on healthcare resource use and associated costs in on-demand users of replacement therapies in von Willebrand disease in France: the FORvWARD study.
Journal: Journal of comparative effectiveness research
Published: March 23, 2026
Real-World Effectiveness and Safety of Concizumab Prophylaxis in Hemophilia: Results From a National French Cohort.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: February 25, 2026
F8 gene variants influence the response to desmopressin in hemophilia A carriers.
Journal: Blood
Published: May 06, 2025
Post-Viral Acquired Idiopathic Purpura Fulminans Caused by Anti-Protein S Antibodies.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: April 19, 2025
Navigating the Transition From Adolescence to Adulthood Among Young People With Severe Haemophilia: The Qualitative Phase of the TRANSHEMO Project.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: February 24, 2025
ORPHEE: A Real-World Study on rIX-FP Prophylaxis Use in Adolescent/Adult Patients With Hemophilia B.
ORPHEE: A Real-World Study on rIX-FP Prophylaxis Use in Adolescent/Adult Patients With Hemophilia B.
Journal: European journal of haematology
Published: September 23, 2024
Assessment of a next generation sequencing gene panel strategy in 133 patients with negative thrombophilia screening.
Journal: Journal of thrombosis and haemostasis : JTH
Published: September 08, 2024
Thrombosis in the perforasome in idiopathic purpura fulminans with anti-protein S antibodies: Anatomical and clinical evidence to improve management.
Journal: Clinical hemorheology and microcirculation
Published: July 20, 2024
Superior Prophylactic Effectiveness of a Recombinant FVIIIFc Over Standard Half-Life FVIII in Hemophilia A: A-SURE Study.
Journal: European journal of haematology
Published: July 08, 2024
Bleeding risk in hemophilia A and B carriers: comparison of factor levels determined using chronometric and chromogenic assays.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: May 03, 2024
Gingival bleeding is a useful clinical feature in the diagnosis of hereditary bleeding disorders in children.
Journal: European journal of pediatrics
Published: December 18, 2023
What is the rationale for mesenchymal stromal cells based therapies in the management of hemophilic arthropathies?
Journal: Osteoarthritis and cartilage
Published: September 18, 2023
Last Updated: 09/26/2026