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A Brassier

Showing results (1-10 of 12) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 27, 2015
[Diagnosing an inborn metabolic error with consciousness disorders]J-B Arnoux, A Brassier, A-S Guemann, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 30, 2011
[Enzyme replacement therapy for lysosomal storage disorders]V Valayannopoulos, A Brassier, A Chabli, et al.
Revue Des Maladies Respiratoires|October 13, 2022
[Pulmonary phenotypes of inborn errors of metabolism]W Mauhin, A Brassier, J London, et al.
JIMD Reports|November 27, 2015
Renal Involvement in a French Paediatric Cohort of Patients with Lysinuric Protein IntoleranceC Nicolas, N Bednarek, V Vuiblet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Journal of Child Neurology|December 17, 2013
Acute psychosis in propionic acidemia: 2 case reportsC Dejean de la Bâtie, V Barbier, V Valayannopoulos, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosisF Habarou, A Brassier, M Rio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 19, 2020
Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysisL Abily-Donval, L Dupic, C Joffre, et al.
JIMD Reports|May 17, 2017
Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 DeficiencyF Habarou, N Bahi-Buisson, E Lebigot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2012
[Prenatal symptoms and diagnosis of inherited metabolic diseases]A Brassier, C Ottolenghi, N Boddaert, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 27, 2015
[Diagnosing an inborn metabolic error with consciousness disorders]J-B Arnoux, A Brassier, A-S Guemann, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 30, 2011
[Enzyme replacement therapy for lysosomal storage disorders]V Valayannopoulos, A Brassier, A Chabli, et al.
Revue Des Maladies Respiratoires|October 13, 2022
[Pulmonary phenotypes of inborn errors of metabolism]W Mauhin, A Brassier, J London, et al.
JIMD Reports|November 27, 2015
Renal Involvement in a French Paediatric Cohort of Patients with Lysinuric Protein IntoleranceC Nicolas, N Bednarek, V Vuiblet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Journal of Child Neurology|December 17, 2013
Acute psychosis in propionic acidemia: 2 case reportsC Dejean de la Bâtie, V Barbier, V Valayannopoulos, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosisF Habarou, A Brassier, M Rio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 19, 2020
Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysisL Abily-Donval, L Dupic, C Joffre, et al.
JIMD Reports|May 17, 2017
Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 DeficiencyF Habarou, N Bahi-Buisson, E Lebigot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 14, 2012
[Prenatal symptoms and diagnosis of inherited metabolic diseases]A Brassier, C Ottolenghi, N Boddaert, et al.
Pageof 2