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 Allaneau

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Annales De Pediatrie|September 1, 1977
[Fabry's disease in children. Clinical and biological study of one family. Structure and ultrastructure of the kidney in a hemizygote and a heterozygote]J C Desbois, J C Mazière, M C Gubler, et al.
Presse Medicale (Paris, France : 1983)|November 26, 1983
[Neonatal hemolysis secondary to congenital poikilocytosis]F Gretillat, N Delepine, D Dhermy, et al.
Archives Francaises De Pediatrie|January 1, 1973
[Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy]J M Saudubray, L Cathelineau, C Charpentier, et al.
Annales D'Endocrinologie|September 1, 1972
[Familial pheochromocytoma]P Seringe, S R Perelman, B Plainfosse, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Annales De Pediatrie|September 1, 1977
[Fabry's disease in children. Clinical and biological study of one family. Structure and ultrastructure of the kidney in a hemizygote and a heterozygote]J C Desbois, J C Mazière, M C Gubler, et al.
Presse Medicale (Paris, France : 1983)|November 26, 1983
[Neonatal hemolysis secondary to congenital poikilocytosis]F Gretillat, N Delepine, D Dhermy, et al.
Archives Francaises De Pediatrie|January 1, 1973
[Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy]J M Saudubray, L Cathelineau, C Charpentier, et al.
Annales D'Endocrinologie|September 1, 1972
[Familial pheochromocytoma]P Seringe, S R Perelman, B Plainfosse, et al.
Pageof 2