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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 behavior
F 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 syndrome
N 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 mutations
T 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 test
J 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 deficiency
A 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 children
D Guimber, D Debray, A Bocquet, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 79) with videos related to
Sort By:
Page
of 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 behavior
F 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 syndrome
N 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 mutations
T 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 test
J 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 deficiency
A 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 children
D Guimber, D Debray, A Bocquet, et al.
Page
of 8