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B Arnoux

Showing results (81-90 of 92) with videos related to

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Experientia|August 15, 1979
The structure of amoorastatone and the cytotoxic limonoid 12-hydroxyamoorastatinJ Polonsky, Z Varon, C Marazano, et al.
Clinical Genetics|May 13, 2014
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinismC Saint-Martin, Q Zhou, G M Martin, et al.
Molecular Genetics and Metabolism Reports|June 7, 2024
Joint replacement risk is markedly increased in alkaptonuria (AKU) in those with prior arthroplastyL R Ranganath, M Khedr, B P Norman, 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|December 21, 2007
Risk assessment of acute vascular events in congenital disorder of glycosylation type IaJ B Arnoux, N Boddaert, V Valayannopoulos, et al.
Scientific Reports|September 28, 2022
Determinants of tyrosinaemia during nitisinone therapy in alkaptonuriaL R Ranganath, A M Milan, A T Hughes, et al.
Journal of Inherited Metabolic Disease|March 12, 2009
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B(12)V Valayannopoulos, L Hubert, J F Benoist, et al.
Journal of Inherited Metabolic Disease|December 20, 2012
Treatment of acute decompensation of maple syrup urine disease in adult patients with a new parenteral amino-acid mixtureA Servais, J B Arnoux, C Lamy, 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.
Journal of Medical Genetics|August 6, 2010
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinismC Bellanné-Chantelot, C Saint-Martin, M-J Ribeiro, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Experientia|August 15, 1979
The structure of amoorastatone and the cytotoxic limonoid 12-hydroxyamoorastatinJ Polonsky, Z Varon, C Marazano, et al.
Clinical Genetics|May 13, 2014
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinismC Saint-Martin, Q Zhou, G M Martin, et al.
Molecular Genetics and Metabolism Reports|June 7, 2024
Joint replacement risk is markedly increased in alkaptonuria (AKU) in those with prior arthroplastyL R Ranganath, M Khedr, B P Norman, 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|December 21, 2007
Risk assessment of acute vascular events in congenital disorder of glycosylation type IaJ B Arnoux, N Boddaert, V Valayannopoulos, et al.
Scientific Reports|September 28, 2022
Determinants of tyrosinaemia during nitisinone therapy in alkaptonuriaL R Ranganath, A M Milan, A T Hughes, et al.
Journal of Inherited Metabolic Disease|March 12, 2009
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B(12)V Valayannopoulos, L Hubert, J F Benoist, et al.
Journal of Inherited Metabolic Disease|December 20, 2012
Treatment of acute decompensation of maple syrup urine disease in adult patients with a new parenteral amino-acid mixtureA Servais, J B Arnoux, C Lamy, 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.
Journal of Medical Genetics|August 6, 2010
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinismC Bellanné-Chantelot, C Saint-Martin, M-J Ribeiro, et al.
Pageof 10