Kolexia
Cano Aline
Pédiatrie
Hôpital La Timone Enfants
Marseille, France
114 Activités
109 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Urgences Maladies rares Maladies mitochondriales Épilepsie Phénylcétonuries Rhabdomyolyse Erreurs innées du métabolisme Encéphalopathies Aminoacidopathies congénitales

Industries

Sanofi
3 collaboration(s)
Dernière en 2022
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Dernières activités

Erratum to: Building bridges for innovation in ageing: Synergies between action groups of the EIP on AHA
The journal of nutrition, health & aging   01 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
French recommendations for the management of glycogen storage disease type III.
European journal of medical research   24 juillet 2023
Executive functions in preschool children with moderate hyperphenylalaninemia and phenylketonuria: a prospective study.
Orphanet journal of rare diseases   03 juillet 2023
Long-term follow-up of 64 children with classical infantile-onset Pompe disease since 2004: A French real-life observational study.
European journal of neurology   10 juin 2023
Clinical, genetic and therapeutic aspects in Menkes disease: study of a French cohort and systematic literature review
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference   01 mai 2023
(198) Non-Aspergillus Fumigatus Mold Infections (NAFMI) in Lung Transplant (LT) Recipients, Pathogens and Risk Factors
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation   01 avril 2023
Systemic corticosteroids for the treatment of acute episodes of rhabdomyolysis in lipin-1-deficient patients.
Journal of inherited metabolic disease   03 février 2023
Neuropsychological Disorders in Moderate Hyperphenylalaninemia: Literature Review.
Developmental neuropsychology   03 janvier 2023
Homocystinurie par déficit en cytathionine-bêta-synthase (CBS)
HAS Publications   13 décembre 2022