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 (91-100 of 210) with videos related to

Pageof 21
Sort By:
Respiration; International Review of Thoracic Diseases|January 1, 1997
Sleep-related hypoxaemia in chronic obstructive pulmonary disease: causes, consequences and treatmentE Weitzenblum, A Chaouat, C Charpentier, et al.
Annales De Pediatrie|May 1, 1979
[Propionicacidemia. A report on two cases (author's transl)]J Costil, A Debard, A Guilhaume, et al.
Archives Francaises De Pediatrie|January 1, 1973
[Constitutional hyperammonemia with carbamoylphosphate synthetase deficiency. Course treatment during dietetic]M Odievre, C Charpentier, L Cathelineau, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Hyperammonemia secondary to hereditary organic acidurias: a study of 29 casesJ M Saudubray, F X Coudé, H Ogier, et al.
The Journal of Pediatrics|September 1, 1983
Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother. Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndromeJ P Harpey, C Charpentier, S I Goodman, et al.
Pediatric Research|January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosisF X Coude, H Ogier, A Munnich, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 27, 1984
Analysis of dipeptides in urine by gas chromatography/mass spectrometry: implications for collagen breakdown in iminodipeptiduria following a study of the dipeptides by electron impact and chemical ionizationC Charpentier, R A Johnstone, A Lemonnier, et al.
Lancet (London, England)|September 8, 1990
Secondary metabolic defects in spinal muscular atrophy type IIJ P Harpey, C Charpentier, M Paturneau-Jouas, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|January 8, 1980
[Propionicacidemia. A report on two cases (author's transl)]J Costil, A Debard, A Guilhaume, et al.
Pediatrics|October 1, 1974
Prenatal diagnosis of methylmalonic aciduriaD Gompertz, P A Goodey, J M Saudubray, et al.
Pageof 21

Showing results (91-100 of 210) with videos related to

Sort By:
Pageof 21
Respiration; International Review of Thoracic Diseases|January 1, 1997
Sleep-related hypoxaemia in chronic obstructive pulmonary disease: causes, consequences and treatmentE Weitzenblum, A Chaouat, C Charpentier, et al.
Annales De Pediatrie|May 1, 1979
[Propionicacidemia. A report on two cases (author's transl)]J Costil, A Debard, A Guilhaume, et al.
Archives Francaises De Pediatrie|January 1, 1973
[Constitutional hyperammonemia with carbamoylphosphate synthetase deficiency. Course treatment during dietetic]M Odievre, C Charpentier, L Cathelineau, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Hyperammonemia secondary to hereditary organic acidurias: a study of 29 casesJ M Saudubray, F X Coudé, H Ogier, et al.
The Journal of Pediatrics|September 1, 1983
Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother. Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndromeJ P Harpey, C Charpentier, S I Goodman, et al.
Pediatric Research|January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosisF X Coude, H Ogier, A Munnich, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 27, 1984
Analysis of dipeptides in urine by gas chromatography/mass spectrometry: implications for collagen breakdown in iminodipeptiduria following a study of the dipeptides by electron impact and chemical ionizationC Charpentier, R A Johnstone, A Lemonnier, et al.
Lancet (London, England)|September 8, 1990
Secondary metabolic defects in spinal muscular atrophy type IIJ P Harpey, C Charpentier, M Paturneau-Jouas, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|January 8, 1980
[Propionicacidemia. A report on two cases (author's transl)]J Costil, A Debard, A Guilhaume, et al.
Pediatrics|October 1, 1974
Prenatal diagnosis of methylmalonic aciduriaD Gompertz, P A Goodey, J M Saudubray, et al.
Pageof 21