Kolexia
Gardin Antoine
Pédiatrie
Hôpital Bicêtre
Le Kremlin-Bicêtre, France
23 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Cholestase Maladies du foie Glycogénose de type III Glycogénose Démence de Pick Carcinomes Maladie de Niemann-Pick de type C Maladies de Niemann-Pick Mucopolysaccharidose de type I

Industries

Sanofi
1 collaboration(s)
Dernière en 2018
Laboratoires Expanscience
1 collaboration(s)
Dernière en 2018
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Dernières activités

Failure of cholic acid therapy in a child with a bile acid synthesis defect and harboring plectin mutations.
Journal of pediatric gastroenterology and nutrition   01 mars 2024
∆ -3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid.
Orphanet journal of rare diseases   07 décembre 2023
Current limitations of gene therapy for rare pediatric diseases: Lessons learned from clinical experience with AAV vectors.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie   05 décembre 2023
A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III.
The Journal of clinical investigation   28 novembre 2023
and Mutations in a Child Presenting With Incomplete Alagille Syndrome.
JPGN reports   17 juillet 2023
Gene therapy for inherited liver disease - Journée Recherche 2023
Youtube @ Filière de Santé Maladies Rares du Foie - FILFOIE   13 juillet 2023
Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy.
JHEP reports : innovation in hepatology   13 juillet 2023
Pathological modeling of glycogen storage disease type III with CRISPR/Cas9 edited human pluripotent stem cells.
Frontiers in cell and developmental biology   11 mai 2023
Long term follow-up after haematopoietic stem cell transplantation for mucopolysaccharidosis type I-H: a retrospective study of 51 patients.
Bone marrow transplantation   09 décembre 2022
A Retrospective Multicentric Study of 34 Patients with Niemann-Pick Type C Disease and Early Liver Involvement in France.
The Journal of pediatrics   17 octobre 2022