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Anne Davit-Spraul

Showing results (11-20 of 29) with videos related to

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Hepatology (Baltimore, Md.)|March 17, 2010
ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural historyAnne Davit-Spraul, Monique Fabre, Sophie Branchereau, et al.
Hepatology (Baltimore, Md.)|February 27, 2015
Targeted pharmacotherapy in progressive familial intrahepatic cholestasis type 2: Evidence for improvement of cholestasis with 4-phenylbutyrateEmmanuel Gonzales, Brigitte Grosse, Brice Schuller, et al.
Hepatology (Baltimore, Md.)|August 18, 2016
MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion diseaseEmmanuel Gonzales, Sarah A Taylor, Anne Davit-Spraul, et al.
Molecular Genetics and Metabolism|June 8, 2011
Liver glycogen storage diseases due to phosphorylase system deficiencies: diagnosis thanks to non invasive blood enzymatic and molecular studiesAnne Davit-Spraul, Monique Piraud, Dries Dobbelaere, et al.
Journal of Hepatology|August 31, 2010
Relapsing features of bile salt export pump deficiency after liver transplantation in two patients with progressive familial intrahepatic cholestasis type 2Giuseppe Maggiore, Emmanuel Gonzales, Marco Sciveres, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 14, 2017
Bile Acid Synthesis Disorders in Arabs: A 10-year Screening StudyAbdulrahman A Al-Hussaini, Kenneth D R Setchell, Badr AlSaleem, et al.
Molecular Genetics and Metabolism|June 11, 2008
Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutationsAnne Davit-Spraul, Catherine Costa, Mokhtar Zater, et al.
Transplantation|October 24, 2014
Improvement of hepatocyte transplantation efficiency in the mdr2-/- mouse model by glyceryl trinitrateLyes Boudechiche, Hadrien Tranchart, Sophie Branchereau, et al.
Gastroenterology|July 23, 2009
Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapyEmmanuel Gonzales, Marie F Gerhardt, Monique Fabre, et al.
Hepatology (Baltimore, Md.)|October 18, 2015
A functional classification of ABCB4 variations causing progressive familial intrahepatic cholestasis type 3Jean-Louis Delaunay, Anne-Marie Durand-Schneider, Claire Dossier, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Hepatology (Baltimore, Md.)|March 17, 2010
ATP8B1 and ABCB11 analysis in 62 children with normal gamma-glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): phenotypic differences between PFIC1 and PFIC2 and natural historyAnne Davit-Spraul, Monique Fabre, Sophie Branchereau, et al.
Hepatology (Baltimore, Md.)|February 27, 2015
Targeted pharmacotherapy in progressive familial intrahepatic cholestasis type 2: Evidence for improvement of cholestasis with 4-phenylbutyrateEmmanuel Gonzales, Brigitte Grosse, Brice Schuller, et al.
Hepatology (Baltimore, Md.)|August 18, 2016
MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion diseaseEmmanuel Gonzales, Sarah A Taylor, Anne Davit-Spraul, et al.
Molecular Genetics and Metabolism|June 8, 2011
Liver glycogen storage diseases due to phosphorylase system deficiencies: diagnosis thanks to non invasive blood enzymatic and molecular studiesAnne Davit-Spraul, Monique Piraud, Dries Dobbelaere, et al.
Journal of Hepatology|August 31, 2010
Relapsing features of bile salt export pump deficiency after liver transplantation in two patients with progressive familial intrahepatic cholestasis type 2Giuseppe Maggiore, Emmanuel Gonzales, Marco Sciveres, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 14, 2017
Bile Acid Synthesis Disorders in Arabs: A 10-year Screening StudyAbdulrahman A Al-Hussaini, Kenneth D R Setchell, Badr AlSaleem, et al.
Molecular Genetics and Metabolism|June 11, 2008
Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutationsAnne Davit-Spraul, Catherine Costa, Mokhtar Zater, et al.
Transplantation|October 24, 2014
Improvement of hepatocyte transplantation efficiency in the mdr2-/- mouse model by glyceryl trinitrateLyes Boudechiche, Hadrien Tranchart, Sophie Branchereau, et al.
Gastroenterology|July 23, 2009
Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapyEmmanuel Gonzales, Marie F Gerhardt, Monique Fabre, et al.
Hepatology (Baltimore, Md.)|October 18, 2015
A functional classification of ABCB4 variations causing progressive familial intrahepatic cholestasis type 3Jean-Louis Delaunay, Anne-Marie Durand-Schneider, Claire Dossier, et al.
Pageof 3