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 Hadchouel

Showing results (91-100 of 105) with videos related to

Pageof 11
Sort By:
The Journal of Pediatrics|July 1, 1988
Budd-Chiari syndrome in children: report of 22 casesS Gentil-Kocher, O Bernard, F Brunelle, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liverJ M Scotto, M Hadchouel, M Odievre, et al.
The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.
Hepatology (Baltimore, Md.)|August 29, 2000
JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndromeC Crosnier, T Attié-Bitach, F Encha-Razavi, et al.
The Journal of Pediatrics|January 1, 1990
Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)F Zhang, J F Deleuze, A Aurias, et al.
The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.
Journal of Hepatology|February 7, 1998
Expression of the liver Na+-independent organic anion transporting polypeptide (oatp-1) in rats with bile duct ligationM Dumont, E Jacquemin, C D'Hont, et al.
Journal of Virology|February 1, 1988
Rearrangement of a common cellular DNA domain on chromosome 4 in human primary liver tumorsC Pasquinelli, F Garreau, L Bougueleret, et al.
Genomics|June 10, 1995
Construction of a 3.7-Mb physical map within human chromosome 20p12 ordering 18 markers in the Alagille syndrome locusN Pollet, S Dhorne-Pollet, J F Deleuze, et al.
Human Genetics|December 1, 1994
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 casesP Labrune, A Myara, M Hadchouel, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
The Journal of Pediatrics|July 1, 1988
Budd-Chiari syndrome in children: report of 22 casesS Gentil-Kocher, O Bernard, F Brunelle, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liverJ M Scotto, M Hadchouel, M Odievre, et al.
The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.
Hepatology (Baltimore, Md.)|August 29, 2000
JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndromeC Crosnier, T Attié-Bitach, F Encha-Razavi, et al.
The Journal of Pediatrics|January 1, 1990
Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)F Zhang, J F Deleuze, A Aurias, et al.
The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.
Journal of Hepatology|February 7, 1998
Expression of the liver Na+-independent organic anion transporting polypeptide (oatp-1) in rats with bile duct ligationM Dumont, E Jacquemin, C D'Hont, et al.
Journal of Virology|February 1, 1988
Rearrangement of a common cellular DNA domain on chromosome 4 in human primary liver tumorsC Pasquinelli, F Garreau, L Bougueleret, et al.
Genomics|June 10, 1995
Construction of a 3.7-Mb physical map within human chromosome 20p12 ordering 18 markers in the Alagille syndrome locusN Pollet, S Dhorne-Pollet, J F Deleuze, et al.
Human Genetics|December 1, 1994
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 casesP Labrune, A Myara, M Hadchouel, et al.
Pageof 11