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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 14, 2005
[Neonatal epilepsy and inborn errors of metabolism]N Bahi-Buisson, K Mention, P L Léger, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 2013
[Suicide attempts by young adolescents: epidemiological characteristics of 517 15-year-old or younger adolescents admitted in French emergency departments]P Giraud, C Fortanier, G Fabre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 7, 2007
[Failure to thrive and psychomotor regression revealing vitamin B12 deficiency in 3 infants]C Mathey, J-N Di Marco, A Poujol, et al.
American Journal of Medical Genetics|October 23, 1997
Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chainB Chabrol, S Sigaudy, V Paquis, et al.
Biomed Research International|June 29, 2018
Muscle Shortening and Spastic Cocontraction in Gastrocnemius Medialis and Peroneus Longus in Very Young Hemiparetic ChildrenM Vinti, N Bayle, A Merlo, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome]O Delmas, C Marrec, E Caietta, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 2015
Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndromeT Busa, M Milh, N Degardin, et al.
Journal of Medical Genetics|May 6, 2014
Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlationsM Bricout, D Grévent, A S Lebre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 5, 2011
[Infratentorial ischemic stroke in children: Three case reports]M Ouattara-Doumbia, A-G Le Moing, E Bourel-Ponchel, et al.
Revue Neurologique|April 29, 2014
[Aspect of brain MRI in mitochondrial respiratory chain deficiency. A diagnostic algorithm of the most common mitochondrial genetic mutations]M Devaux-Bricout, D Grévent, A-S Lebre, et al.
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