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F Feillet

Showing results (61-70 of 79) with videos related to

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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|March 13, 2016
[Early origins of adult disease]U Simeoni, 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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 14, 2015
[Complementary feeding: Evolving concepts and recommendations]D Turck, C Dupont, M Vidailhet, 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.
Journal of Medical Genetics|August 4, 2010
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutationsT Dupré, S Vuillaumier-Barrot, I Chantret, et al.
Clinical Genetics|January 13, 2016
Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic testJ Thevenon, Y Duffourd, A Masurel-Paulet, 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.
Molecular Genetics and Metabolism|May 10, 2011
Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiencyA Boutron, C Acquaviva, C Vianey-Saban, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 11, 2021
The role of nutrition in non-alcoholic fatty liver disease treatment in obese childrenD Guimber, D Debray, A Bocquet, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
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|March 13, 2016
[Early origins of adult disease]U Simeoni, 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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 14, 2015
[Complementary feeding: Evolving concepts and recommendations]D Turck, C Dupont, M Vidailhet, 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.
Journal of Medical Genetics|August 4, 2010
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutationsT Dupré, S Vuillaumier-Barrot, I Chantret, et al.
Clinical Genetics|January 13, 2016
Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic testJ Thevenon, Y Duffourd, A Masurel-Paulet, 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.
Molecular Genetics and Metabolism|May 10, 2011
Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiencyA Boutron, C Acquaviva, C Vianey-Saban, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 11, 2021
The role of nutrition in non-alcoholic fatty liver disease treatment in obese childrenD Guimber, D Debray, A Bocquet, et al.
Pageof 8