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

F X Coude

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Pediatric Research|January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosisF X Coude, H Ogier, A Munnich, et al.
Lancet (London, England)|May 17, 1980
Fatty-acid-responsive alopecia in multiple carboxylase deficiencyA Munnich, J M Saudubray, F X Coude, et al.
The New England Journal of Medicine|December 14, 1978
Dichloroacetate as treatment for congenital lactic acidosisF X Coude, J M Saudubray, F DeMaugre, et al.
Biochimie|January 1, 1983
Developmental changes of citrullinogenesis, mitochondrial N-acetylglutamate content and N-acetylglutamate synthetase in fetal and neonatal ratsD Rabier, P Briand, F X Coude, et al.
Archives Francaises De Pediatrie|January 1, 1980
[Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)]J M Saudubray, C Charpentier, F X Coude, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1987
Results of 1-year growth hormone (GH)-releasing hormone-(1-44) treatment on growth, somatomedin-C, and 24-hour GH secretion in six children with partial GH deficiencyP E Rochiccioli, M T Tauber, F X Coude, et al.
Pediatrics|January 1, 1982
Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemiaF X Coude, H Ogier, G Grimber, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuriaM Rodes, A Ribes, M Pineda, et al.
Archives Francaises De Pediatrie|December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]F X Coude, H Ogier, C Charpentier, et al.
Human Genetics|January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorderF X Coude, H Ogier, C Charpentier, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Pediatric Research|January 1, 1982
Defective insulin response to intravenous glucose in congenital lactic acidosisF X Coude, H Ogier, A Munnich, et al.
Lancet (London, England)|May 17, 1980
Fatty-acid-responsive alopecia in multiple carboxylase deficiencyA Munnich, J M Saudubray, F X Coude, et al.
The New England Journal of Medicine|December 14, 1978
Dichloroacetate as treatment for congenital lactic acidosisF X Coude, J M Saudubray, F DeMaugre, et al.
Biochimie|January 1, 1983
Developmental changes of citrullinogenesis, mitochondrial N-acetylglutamate content and N-acetylglutamate synthetase in fetal and neonatal ratsD Rabier, P Briand, F X Coude, et al.
Archives Francaises De Pediatrie|January 1, 1980
[Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)]J M Saudubray, C Charpentier, F X Coude, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1987
Results of 1-year growth hormone (GH)-releasing hormone-(1-44) treatment on growth, somatomedin-C, and 24-hour GH secretion in six children with partial GH deficiencyP E Rochiccioli, M T Tauber, F X Coude, et al.
Pediatrics|January 1, 1982
Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemiaF X Coude, H Ogier, G Grimber, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuriaM Rodes, A Ribes, M Pineda, et al.
Archives Francaises De Pediatrie|December 1, 1981
[Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]]F X Coude, H Ogier, C Charpentier, et al.
Human Genetics|January 1, 1981
Neonatal glutaric aciduria type II: an X-linked recessive inherited disorderF X Coude, H Ogier, C Charpentier, et al.
Pageof 3