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Clinical Genetics|January 7, 2011
Twenty-five novel mutations including duplications in the ATP7A geneM-P Moizard, N Ronce, S Blesson, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]F Feillet, H Ogier, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 2017
Vitamin A in pediatrics: An update from the Nutrition Committee of the French Society of PediatricsM Vidailhet, D Rieu, F Feillet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 17, 2018
Parenteral nutrition for preterm infants: Issues and strategyD Darmaun, A Lapillonne, U Simeoni, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2019
Nutritional risks of ARFID (avoidant restrictive food intake disorders) and related behaviorF Feillet, A Bocquet, A Briend, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 20, 2018
Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)B Chabrol, P Jacquin, L Francois, et al.
Acta Neurologica Scandinavica|April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 15, 2022
"Baby-led weaning" - Progress in infant feeding or risky trend?A Bocquet, S Brancato, D Turck, et al.
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