Kolexia
Panuel Michel
Radio-diagnostic
Hôpital Nord Marseille
Marseille, France
74 Activités
3 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Maladies osseuses Splénose Traumatismes cranioencéphaliques Tuberculose COVID-19 Hématome subdural Tuberculose ostéoarticulaire Hémorragie Ostéochondrodysplasies

Industries

Sanofi
9 collaboration(s)
Dernière en 2023
Ipsen
5 collaboration(s)
Dernière en 2021
INOZYME PHARMA, INC.
2 collaboration(s)
Dernière en 2022
Alexion
2 collaboration(s)
Dernière en 2021

Dernières activités

A pathological Neandertal thumb phalanx from Moula-Guercy (France).
International journal of paleopathology   22 juin 2023
Exploration of the fetal skeleton by ultra-low-dose computed tomography: guidelines from the Fetal Imaging Task Force of the European Society of Paediatric Radiology.
Pediatric radiology   27 août 2022
Fetal facial bone growth: Post-mortem CT analysis.
Morphologie : bulletin de l'Association des anatomistes   21 juin 2022
Correction to: Incidence of child abuse with subdural hemorrhage during the first year of the COVID-19 pandemic: a nationwide study in France.
European journal of pediatrics   18 mai 2022
Bilateral and symmetrical enchondromatosis lesions: clinical, radiologic and genetic findings
Abstracts from the 54th European Society of Human Genetics (ESHG) Conference   01 avril 2022
Incidence of child abuse with subdural hemorrhage during the first year of the COVID-19 pandemic: a nationwide study in France.
European journal of pediatrics   17 mars 2022
Relevance of Routine Abdominopelvic Ultrasound in Suspected Child Abuse in Children Under 2 years of Age: Review of 15 years of Experience.
Child maltreatment   19 novembre 2021
Échographie dans l’exploration du scrotum aigu chez l’enfant
Journal d'imagerie diagnostique et interventionnelle   01 avril 2020
Thoracic ultrasound accuracy for the investigation of initial neonatal respiratory distress.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie   17 octobre 2019
Heterozygous FGFR1 mutation may be responsible for an incomplete form of osteoglophonic dysplasia, characterized only by radiolucent bone lesions and teeth retentions.
European journal of medical genetics   15 juillet 2019