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B Chabrol

Showing results (121-130 of 173) with videos related to

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Journal of Medical Genetics|June 17, 2003
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasiaN Philip, B Chabrol, A-M Lossi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 7, 2014
[Value of routine identification of respiratory infectious agents in children hospitalized with an acute asthma exacerbation]E Sauvaget, V Bresson, M Oudyi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 9, 2013
[Evaluation of the abstracts submitted to the French Society of Pediatrics (SFP) in 2012]A Testefort, B Giraudeau, T Lamireau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2003
[Restrictive cardiomyopathy due to myofibrillar myopathy]I Ligi, A Fraisse, B Chabrol, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 4, 2017
[Teaching pediatrics to residents via conventional lectures in France: A national survey from students]B Girard, M Bendavid, J-C Faivre, et al.
Pediatric Nephrology (Berlin, Germany)|August 24, 2000
Chronic renal failure and portal hypertension--is portosystemic shunt indicated?M Tsimaratos, S Cloarec, B Roquelaure, et al.
European Journal of Pediatrics|July 1, 1995
Early-onset fatal encephalomyopathy associated with severe mtDNA depletionV Paquis-Flucklinger, J F Pellissier, J Camboulives, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 26, 2016
[Chest X-ray and acute bronchiolitis: Are these indications decreasing?]V Arnoux, A Carsin, E Bosdure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature reviewM-V André, P Cacciagli, A Cano, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 12, 2018
Infant botulism: Two case reports and electroneuromyogram findingsJ Bernardor, J Neveu, H Haas, et al.
Pageof 18

Showing results (121-130 of 173) with videos related to

Sort By:
Pageof 18
Journal of Medical Genetics|June 17, 2003
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasiaN Philip, B Chabrol, A-M Lossi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 7, 2014
[Value of routine identification of respiratory infectious agents in children hospitalized with an acute asthma exacerbation]E Sauvaget, V Bresson, M Oudyi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 9, 2013
[Evaluation of the abstracts submitted to the French Society of Pediatrics (SFP) in 2012]A Testefort, B Giraudeau, T Lamireau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2003
[Restrictive cardiomyopathy due to myofibrillar myopathy]I Ligi, A Fraisse, B Chabrol, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 4, 2017
[Teaching pediatrics to residents via conventional lectures in France: A national survey from students]B Girard, M Bendavid, J-C Faivre, et al.
Pediatric Nephrology (Berlin, Germany)|August 24, 2000
Chronic renal failure and portal hypertension--is portosystemic shunt indicated?M Tsimaratos, S Cloarec, B Roquelaure, et al.
European Journal of Pediatrics|July 1, 1995
Early-onset fatal encephalomyopathy associated with severe mtDNA depletionV Paquis-Flucklinger, J F Pellissier, J Camboulives, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 26, 2016
[Chest X-ray and acute bronchiolitis: Are these indications decreasing?]V Arnoux, A Carsin, E Bosdure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature reviewM-V André, P Cacciagli, A Cano, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 12, 2018
Infant botulism: Two case reports and electroneuromyogram findingsJ Bernardor, J Neveu, H Haas, et al.
Pageof 18