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Research and Practice in Thrombosis and Haemostasis|March 9, 2026
Platelet dense granule defect: experience in the French populationDelphine Borgel, Agathe Beauvais, Cécile Bally, et al.Journal of Thrombosis and Haemostasis : JTH|May 28, 2025
Health-related quality of life in children with von Willebrand disease: results of the French real-life Willebrand Study Health-related Quality of Life studyJenny Goudemand, Sophie Susen, Claire Berger, et al.Journal of Neurosurgery. Pediatrics|January 1, 2021
Etiology of intracerebral hemorrhage in children: cohort study, systematic review, and meta-analysisGrégoire Boulouis, Sarah Stricker, Sandro Benichi, et al.Journal of Inherited Metabolic Disease|April 9, 2020
Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylationAnna Čechová, Ruqaiah Altassan, Delphine Borgel, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2025
Navigating the Transition From Adolescence to Adulthood Among Young People With Severe Haemophilia: The Qualitative Phase of the TRANSHEMO ProjectMarie-Anaïs Roques, Natacha Rosso-Delsemme, Amandine Celli, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|August 12, 2023
Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross-sectional study based on the FranceCoag registryNgoc Anh Thu Nguyen, Pascal Auquier, Any Beltran Anzola, et al.European Journal of Haematology|December 5, 2024
ORPHEE: A Real-World Study on rIX-FP Prophylaxis Use in Adolescent/Adult Patients With Hemophilia BFabienne Volot, Sabine Castet, Alexandra Fournel, et al.Journal of Thrombosis and Haemostasis : JTH|October 28, 2020
Gastrointestinal bleeding from angiodysplasia in von Willebrand disease: Improved diagnosis and outcome prediction using videocapsule on top of conventional endoscopyAntoine Rauch, Camille Paris, Yohann Repesse, et al.Molecular Genetics and Metabolism|August 5, 2023
Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute managementCamille Wicker, Charles-Joris Roux, Louise Goujon, et al.Orphanet Journal of Rare Diseases|March 12, 2025
Gynecological issues in children and adolescents seen at rare-disease referral centers: an observational retrospective cohort studyIphigénie Cavadias, Magali Viaud, Marie Falampin, et al.Pageof 6