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M Hadchouel

Showing results (81-90 of 105) with videos related to

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Hepatology (Baltimore, Md.)|April 1, 1996
Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasisJ F Deleuze, E Jacquemin, C Dubuisson, et al.
The Journal of Pediatrics|March 1, 1986
Liver disease associated with anti-liver-kidney microsome antibody in childrenG Maggiore, O Bernard, J C Homberg, et al.
Cell|February 23, 1996
Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndromeM Pontoglio, J Barra, M Hadchouel, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 1, 1993
Autoimmune hepatitis associated with anti-actin antibodies in children and adolescentsG Maggiore, F Veber, O Bernard, et al.
Hepatology (Baltimore, Md.)|May 1, 1983
Seroimmunologic classification of chronic hepatitis in 57 childrenM Odièvre, G Maggiore, J C Homberg, et al.
The Journal of Pediatrics|August 1, 1987
Sclerosing cholangitis with neonatal onsetO Amedee-Manesme, O Bernard, F Brunelle, et al.
Hepatology (Baltimore, Md.)|January 1, 1985
A retrospective study of the role of delta agent infection in children with HBsAg-positive chronic hepatitisG Maggiore, M Hadchouel, F Sessa, et al.
Gastroenterology|April 30, 1999
Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndromeC Crosnier, C Driancourt, N Raynaud, et al.
The Journal of Pediatrics|September 1, 1994
A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiencyE Jacquemin, K D Setchell, N C O'Connell, et al.
Genomics|June 15, 1997
Construction of an integrated physical and gene map of human chromosome 20p12 providing candidate genes for Alagille syndromeN Pollet, C Boccaccio, S Dhorne-Pollet, et al.
Pageof 11

Showing results (81-90 of 105) with videos related to

Sort By:
Pageof 11
Hepatology (Baltimore, Md.)|April 1, 1996
Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasisJ F Deleuze, E Jacquemin, C Dubuisson, et al.
The Journal of Pediatrics|March 1, 1986
Liver disease associated with anti-liver-kidney microsome antibody in childrenG Maggiore, O Bernard, J C Homberg, et al.
Cell|February 23, 1996
Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndromeM Pontoglio, J Barra, M Hadchouel, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 1, 1993
Autoimmune hepatitis associated with anti-actin antibodies in children and adolescentsG Maggiore, F Veber, O Bernard, et al.
Hepatology (Baltimore, Md.)|May 1, 1983
Seroimmunologic classification of chronic hepatitis in 57 childrenM Odièvre, G Maggiore, J C Homberg, et al.
The Journal of Pediatrics|August 1, 1987
Sclerosing cholangitis with neonatal onsetO Amedee-Manesme, O Bernard, F Brunelle, et al.
Hepatology (Baltimore, Md.)|January 1, 1985
A retrospective study of the role of delta agent infection in children with HBsAg-positive chronic hepatitisG Maggiore, M Hadchouel, F Sessa, et al.
Gastroenterology|April 30, 1999
Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndromeC Crosnier, C Driancourt, N Raynaud, et al.
The Journal of Pediatrics|September 1, 1994
A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiencyE Jacquemin, K D Setchell, N C O'Connell, et al.
Genomics|June 15, 1997
Construction of an integrated physical and gene map of human chromosome 20p12 providing candidate genes for Alagille syndromeN Pollet, C Boccaccio, S Dhorne-Pollet, et al.
Pageof 11