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M Vidailhet

Showing results (281-290 of 303) with videos related to

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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.
The British Journal of Nutrition|November 26, 2011
Dietary treatment of cows' milk protein allergy in childhood: a commentary by the Committee on Nutrition of the French Society of PaediatricsC Dupont, J P Chouraqui, D de Boissieu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 24, 2003
[Feeding of infants based on age. Practice guidelines]A Bocquet, J L Bresson, A Briend, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 6, 2004
[Symptomatic rickets in adolescents]E Mallet, J Gaudelus, P Reinert, et al.
Revue Neurologique|February 5, 2017
"De-novo" consultation: Evaluation of an outpatient's clinic dedicated to early diagnosis of parkinsonian syndromesJ Ruggeri, L-L Mariani, S Aix, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 31, 2012
Vitamin D: still a topical matter in children and adolescents. A position paper by the Committee on Nutrition of the French Society of PaediatricsM Vidailhet, E Mallet, A Bocquet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2012
[Malnutrition screening in clinical practice]R Hankard, V Colomb, H Piloquet, et al.
Brain : a Journal of Neurology|May 29, 2000
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?J Tassin, A Dürr, A M Bonnet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 2010
[Dietetic treatment of cow's milk protein allergy]C Dupont, J-P Chouraqui, D de Boissieu, et al.
American Journal of Human Genetics|June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Tassin, A Dürr, T de Broucker, et al.
Pageof 31

Showing results (281-290 of 303) with videos related to

Sort By:
Pageof 31
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.
The British Journal of Nutrition|November 26, 2011
Dietary treatment of cows' milk protein allergy in childhood: a commentary by the Committee on Nutrition of the French Society of PaediatricsC Dupont, J P Chouraqui, D de Boissieu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 24, 2003
[Feeding of infants based on age. Practice guidelines]A Bocquet, J L Bresson, A Briend, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 6, 2004
[Symptomatic rickets in adolescents]E Mallet, J Gaudelus, P Reinert, et al.
Revue Neurologique|February 5, 2017
"De-novo" consultation: Evaluation of an outpatient's clinic dedicated to early diagnosis of parkinsonian syndromesJ Ruggeri, L-L Mariani, S Aix, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 31, 2012
Vitamin D: still a topical matter in children and adolescents. A position paper by the Committee on Nutrition of the French Society of PaediatricsM Vidailhet, E Mallet, A Bocquet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2012
[Malnutrition screening in clinical practice]R Hankard, V Colomb, H Piloquet, et al.
Brain : a Journal of Neurology|May 29, 2000
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?J Tassin, A Dürr, A M Bonnet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 2010
[Dietetic treatment of cow's milk protein allergy]C Dupont, J-P Chouraqui, D de Boissieu, et al.
American Journal of Human Genetics|June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Tassin, A Dürr, T de Broucker, et al.
Pageof 31