Kolexia
Wiedemann Arnaud
Pédiatrie
Hôpital Brabois
Vandoeuvre-lès-Nancy, France
66 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Phénylcétonuries Rachitisme Carence en vitamine B12 Choc septique Urgences Fièvre Paralysie Choc Syndrome de réponse inflammatoire généralisée

Industries

B3TSI
13 collaboration(s)
Dernière en 2023
Bouchara-Recordati
2 collaboration(s)
Dernière en 2023
Axess Research
1 collaboration(s)
Dernière en 2023
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{{person.topindus4.tot}} collaboration(s)
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Dernières activités

Multiomic analysis in fibroblasts of patients with inborn errors of cobalamin metabolism reveals concordance with clinical and metabolic variability.
EBioMedicine   01 janvier 2024
Identification of factors associated with the management of childhood obesity: Results from a French pediatric cohort study.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie   20 novembre 2023
RYR: RhabdomYolyse in Intensive caRe
Essai Clinique (CHU Nancy)   20 octobre 2023
Coma With Hyperammonemia in a Patient With Kwashiorkor.
Gastroenterology research   26 août 2023
Association between acute complications in PMM2-CDG patients and haemostasis anomalies: Data from a multicentric study and suggestions for acute management.
Molecular genetics and metabolism   31 juillet 2023
Procalcitonin is associated with sudden unexpected death in infancy due to infection.
European journal of pediatrics   23 juin 2023
Blood phenylalanine fluctuation in phenylketonuric children treated by BH4 or low-phenylalanine diet from birth.
Scientific reports   12 juin 2023
ALTIPICU: Air Leak Test in Pediatric Intensive Care Unit : a Multicentric and Prospective Study
Essai Clinique (Assistance publique – Hôpitaux de Paris)   09 mai 2023
Efficacy of haematopoietic stem cell boost as a rescue for poor graft function after haematopoietic stem cell transplantation: A multicentre retrospective study on behalf of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC).
British journal of haematology   27 mars 2023
Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B metabolism: A meta-analysis.
Cell reports. Medicine   27 juin 2022