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

M Odievre

Showing results (31-40 of 43) with videos related to

Pageof 5
Sort By:
The Journal of Pediatrics|June 1, 1984
Treatment of autoimmune chronic active hepatitis in childhoodG Maggiore, O Bernard, M Hadchouel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 19, 2003
[Telephone activity in outpatient pediatric practice]R Assathiany, J M Rerolle, C Messica, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1990
Congenital hepatic fibrosis, cystic kidneys, mental retardation, and facial dysmorphy: a new report of an autosomal recessive syndromeP Labrune, J C Lange, P Bedossa, et al.
Archives Francaises De Pediatrie|March 1, 1983
[Functional spontaneous splenorenal anastomosis in portal hypertension due to cavernoma. Apropos of 5 cases reports]M Villard, J P Girardet, J P Montagne, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 1, 1991
Fatal liver failure in two children with Niemann-Pick disease type BP Labrune, P Bedossa, P Huguet, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1992
Bilirubin uridine diphosphate glucuronosyltransferase hepatic activity in jaundice associated with congenital hypothyroidismP Labrune, A Myara, P Huguet, et al.
Acta Paediatrica Scandinavica|June 1, 1990
Recurrent enterocolitis-like symptoms as the possible presenting manifestations of neonatal Brucella melitensis infectionP Labrune, B Jabir, J F Magny, et al.
Archives Francaises De Pediatrie|February 1, 1975
[Fructose 1,6-diphosphatase deficiency in 2 sisters]M Odievre, M Brivet, N Moatti, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 1987
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia)R Habib, J P Dommergues, M C Gubler, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
The long-term outcome of patients with glycogen storage diseasesG P Smit, J Fernandes, J V Leonard, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|June 1, 1984
Treatment of autoimmune chronic active hepatitis in childhoodG Maggiore, O Bernard, M Hadchouel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 19, 2003
[Telephone activity in outpatient pediatric practice]R Assathiany, J M Rerolle, C Messica, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 1, 1990
Congenital hepatic fibrosis, cystic kidneys, mental retardation, and facial dysmorphy: a new report of an autosomal recessive syndromeP Labrune, J C Lange, P Bedossa, et al.
Archives Francaises De Pediatrie|March 1, 1983
[Functional spontaneous splenorenal anastomosis in portal hypertension due to cavernoma. Apropos of 5 cases reports]M Villard, J P Girardet, J P Montagne, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 1, 1991
Fatal liver failure in two children with Niemann-Pick disease type BP Labrune, P Bedossa, P Huguet, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1992
Bilirubin uridine diphosphate glucuronosyltransferase hepatic activity in jaundice associated with congenital hypothyroidismP Labrune, A Myara, P Huguet, et al.
Acta Paediatrica Scandinavica|June 1, 1990
Recurrent enterocolitis-like symptoms as the possible presenting manifestations of neonatal Brucella melitensis infectionP Labrune, B Jabir, J F Magny, et al.
Archives Francaises De Pediatrie|February 1, 1975
[Fructose 1,6-diphosphatase deficiency in 2 sisters]M Odievre, M Brivet, N Moatti, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 1987
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia)R Habib, J P Dommergues, M C Gubler, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
The long-term outcome of patients with glycogen storage diseasesG P Smit, J Fernandes, J V Leonard, et al.
Pageof 5