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

C Charpentier

Showing results (161-170 of 210) with videos related to

Pageof 21
Sort By:
Enzyme|January 1, 1987
Hyperketotic states due to inherited defects of ketolysisJ M Saudubray, N Specola, B Middleton, et al.
Archives Francaises De Pediatrie|December 1, 1982
[Heterogeneity of leucinosis. Correlations between clinical manifestations, protein tolerance and enzyme deficiency]J M Saudubray, O Amédée-Manesme, A Munnich, 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.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.
Archives Francaises De Pediatrie|January 1, 1986
[Incurable keratitis and chronic palmoplantar hyperkeratosis with hypertyrosinemia. Cure using a tyrosine-restricted diet. Type II tyrosinemia]F Hervé, J L Moreno, H Ogier, et al.
Pediatrics|May 1, 1993
Clinical and biochemical phenotype in 11 patients with mevalonic aciduriaG F Hoffmann, C Charpentier, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Hudson memorial lecture. Neonatal management of organic acidurias. Clinical updateJ M Saudubray, H Ogier, C Charpentier, et al.
European Journal of Pediatrics|October 1, 1981
Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosisA Munnich, J M Saudubray, A Cotisson, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|May 25, 2015
Variability of human immunodeficiency virus-1 in the female genital reservoir during genital reactivation of herpes simplex virus type 2J LeGoff, P Roques, M-A Jenabian, et al.
Pageof 21

Showing results (161-170 of 210) with videos related to

Sort By:
Pageof 21
Enzyme|January 1, 1987
Hyperketotic states due to inherited defects of ketolysisJ M Saudubray, N Specola, B Middleton, et al.
Archives Francaises De Pediatrie|December 1, 1982
[Heterogeneity of leucinosis. Correlations between clinical manifestations, protein tolerance and enzyme deficiency]J M Saudubray, O Amédée-Manesme, A Munnich, 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.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1994
[Diagnosis of metabolic coma in children]F Poggi-Travert, B Héron, T Billette de Villemeur, et al.
Archives Francaises De Pediatrie|January 1, 1986
[Incurable keratitis and chronic palmoplantar hyperkeratosis with hypertyrosinemia. Cure using a tyrosine-restricted diet. Type II tyrosinemia]F Hervé, J L Moreno, H Ogier, et al.
Pediatrics|May 1, 1993
Clinical and biochemical phenotype in 11 patients with mevalonic aciduriaG F Hoffmann, C Charpentier, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Hudson memorial lecture. Neonatal management of organic acidurias. Clinical updateJ M Saudubray, H Ogier, C Charpentier, et al.
European Journal of Pediatrics|October 1, 1981
Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosisA Munnich, J M Saudubray, A Cotisson, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|May 25, 2015
Variability of human immunodeficiency virus-1 in the female genital reservoir during genital reactivation of herpes simplex virus type 2J LeGoff, P Roques, M-A Jenabian, et al.
Pageof 21