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Developmental Neuropsychology|January 3, 2023
Neuropsychological Disorders in Moderate Hyperphenylalaninemia: Literature ReviewL Paermentier, A Cano, B Chabrol, et al.Revue Neurologique|September 24, 2008
[Glucose transporter type 1 (GLUT-1) deficiency]A Cano, I Ticus, B ChabrolArchives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 8, 2021
Use of a book to disclose a diagnosis of Duchenne muscular dystrophy to a young child: A pilot studyF Audic, P Catillon, J Berbis, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 21, 2020
Clinical phenotype associated with TANGO2 gene mutationC Hoebeke, A Cano, P De Lonlay, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 11, 2015
[Vitamin D deficiency rickets complicating Dorfman-Chanarin syndrome]C Barraud, A Cano, C Boulay, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 2008
[GLUT-1 deficiency syndrome or De Vivo disease: a case report]I Ticus, A Cano, N Villeneuve, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 11, 2013
[Postinfectious family case of acute necrotizing encephalopathy caused by RANBP2 gene mutation]C Di Meglio, A Cano, M Milh, et al.Respiratory Medicine Case Reports|April 18, 2022
A rare chest tumor in a 7-year old girl with a neurodegenerative diseaseE Benhaïm-Mattout, A Cano, C Di Meglio, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 10, 2002
[Special aspects of pediatric research relevant to the advisory board of protection of biomedical research participants]B ChabrolArchives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 1, 1997
[Ceroid-lipofuscinosis: recent notions]B ChabrolPageof 221