Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Ogier

Showing results (81-90 of 127) with videos related to

Pageof 13
Sort By:
Human Genetics|January 1, 1990
A probable sex difference in mutation rates in ornithine transcarbamylase deficiencyC Bonaïti-Pellié, A Pelet, H Ogier, et al.
Lancet (London, England)|August 13, 1983
Deficient liver biotinidase activity in multiple carboxylase deficiencyM Gaudry, A Munnich, J M Saudubray, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.
Annales De Medecine Interne|January 1, 1986
[Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet]H Ogier, F Hervé, J M Saudubray, et al.
The New England Journal of Medicine|February 15, 1990
Neurologic crises in hereditary tyrosinemiaG Mitchell, J Larochelle, M Lambert, et al.
Journal of Inherited Metabolic Disease|December 20, 2012
Maternal and fetal tyrosinemia type IN Garcia Segarra, S Roche, A Imbard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newbornA Lombes, N B Romero, G Touati, et al.
European Journal of Pediatrics|January 1, 1987
Intellectual and school performances in early-treated classical PKU patients. The French collaborative studyJ M Saudubray, F Rey, H Ogier, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology]A Lombes, F Hervé, H Ogier, et al.
Pageof 13

Showing results (81-90 of 127) with videos related to

Sort By:
Pageof 13
Human Genetics|January 1, 1990
A probable sex difference in mutation rates in ornithine transcarbamylase deficiencyC Bonaïti-Pellié, A Pelet, H Ogier, et al.
Lancet (London, England)|August 13, 1983
Deficient liver biotinidase activity in multiple carboxylase deficiencyM Gaudry, A Munnich, J M Saudubray, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.
Annales De Medecine Interne|January 1, 1986
[Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet]H Ogier, F Hervé, J M Saudubray, et al.
The New England Journal of Medicine|February 15, 1990
Neurologic crises in hereditary tyrosinemiaG Mitchell, J Larochelle, M Lambert, et al.
Journal of Inherited Metabolic Disease|December 20, 2012
Maternal and fetal tyrosinemia type IN Garcia Segarra, S Roche, A Imbard, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newbornA Lombes, N B Romero, G Touati, et al.
European Journal of Pediatrics|January 1, 1987
Intellectual and school performances in early-treated classical PKU patients. The French collaborative studyJ M Saudubray, F Rey, H Ogier, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology]A Lombes, F Hervé, H Ogier, et al.
Pageof 13