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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 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|May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]J M Pinard, C Marsac, E Barkaoui, et al.Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 9, 2014
[Acute bronchiolitis and chest physiotherapy: the end of a reign]B Sterling, E Bosdure, N Stremler-Le Bel, et al.Pediatric Neurology|January 1, 1993
MRI and localized proton MRS in early infantile form of neuronal ceroid-lipofuscinosisS Confort-Gouny, B Chabrol, J Vion-Dury, et al.Neuroradiology|October 1, 1995
Localised proton magnetic resonance spectroscopy in X-linked adrenoleukodystrophyS Confort-Gouny, J Vion-Dury, B Chabrol, 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.Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2003
[Case history of mitochondrial cytopathy with cardiac expression]A Bertrand, A Fraisse, P Chetaille, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 8, 2004
[Isolated agenesia of pulmonary artery]I Boudard, L Mely, A Labbé, et al.Pageof 19