Kolexia
Huguenin Yoann Pédiatrie
Huguenin Yoann
Pédiatrie
Camsp Polyvalent
Bordeaux, France
46 Activités
0 Followers
Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Hémophilie A Maladies de von Willebrand Hémorragie Thrombasthénie Thrombose Anémie Hypertension artérielle Albinisme Thalassémie

Collaborateurs

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Lafarie-Castet Sabine
Lafarie-Castet Sabine
Hôpital Pellegrin, Bordeaux, France
Harroche-Angel Annie
Harroche-Angel Annie
Hôpital Necker Enfants Malades, Paris, France
Fiore Mathieu
Fiore Mathieu
Hôpital Haut-lévêque, Pessac, France
Meunier Sandrine
Meunier Sandrine
Hôpital Louis Pradel, Bron, France

Industries

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Sobi
12 collaboration(s)
Dernière en 2023
Takeda Pharmaceutical
5 collaboration(s)
Dernière en 2022
LFB
5 collaboration(s)
Dernière en 2023
Roche
5 collaboration(s)
Dernière en 2023

Dernières activités

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Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.
Haematologica   22 février 2024
Acquired haemophilia A in paediatric patients: A retrospective French cohort of eight cases.
British journal of haematology   08 janvier 2024
A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD): A Phase 3, Prospective, Multicenter, Uncontrolled, Open-Label Clinical Study to Determine the Efficacy, Safety, and Tolerability of rVWF With or Without ADVATE in the Treatment and Control of Bleeding Episodes, the Efficacy and Safety of rVWF in Elective and Emergency Surgeries, and the Pharmacokinetics (PK) of rVWF in Children Diagnosed With Severe Von Willebrand Disease
Essai Clinique (Shire)   09 novembre 2023
characterization of rare anti-α β isoantibodies produced by patients with Glanzmann thrombasthenia that severely block fibrinogen binding and generate procoagulant platelets via complement activation.
Research and practice in thrombosis and haemostasis   04 novembre 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 registry.
Haemophilia : the official journal of the World Federation of Hemophilia   12 août 2023
Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non-severe haemophilia A.
Haemophilia : the official journal of the World Federation of Hemophilia   06 juillet 2023
Hémophilie
HAS Publications   20 juin 2023
TRANSHEMO: Determinants and Consequences of the Transition to Adulthood Among Adolescents With Haemophilia - TRANSHEMO
Essai Clinique (Assistance publique - Hôpitaux de Marseille)   13 février 2023
High Rates of Anti-αIIbβ3 Antibodies Produced by a Glanzmann Thrombasthenia Patient after First and Unique Red Blood Cells Administration.
Acta haematologica   14 septembre 2022
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
American journal of hematology   02 septembre 2022