Search research articles
Contact Us
Filters
Showing results (11-20 of 96) with videos related to
Page
of 10
Sort By:
Frontiers in Bioscience (Landmark Edition)
|
March 11, 2009
Liver diseases related to MDR3 (ABCB4) gene deficiency
Emmanuel Gonzales, Anne Davit-Spraul, Christiane Baussan, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 5, 2022
A Model for Early Endoscopic Detection of High-Risk Gastroesophageal Varices in Children With Biliary Atresia
Oanez Ackermann, Paul de Boissieu, Olivier Bernard, et al.
European Journal of Medical Genetics
|
May 15, 2021
Defining the natural history of rare genetic liver diseases: Lessons learned from the NAPPED initiative
Daan B E van Wessel, Emmanuel Gonzales, Bettina E Hansen, et al.
Pediatric Radiology
|
February 23, 2018
Diagnosis, treatment and outcome of hepatic venous outflow obstruction in paediatric liver transplantation: 24-year experience at a single centre
Alexis Galloux, Erika Pace, Stephanie Franchi-Abella, et al.
Molecular Genetics and Metabolism
|
August 3, 2014
Liver transcript analysis reveals aberrant splicing due to silent and intronic variations in the ABCB11 gene
Anne Davit-Spraul, Christophe Oliveira, Emmanuel Gonzales, et al.
Journal of Hepatology
|
May 22, 2012
Successful mutation-specific chaperone therapy with 4-phenylbutyrate in a child with progressive familial intrahepatic cholestasis type 2
Emmanuel Gonzales, Brigitte Grosse, Doris Cassio, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 17, 2016
Long-term successful liver-kidney transplantation in a child with atypical hemolytic uremic syndrome caused by homozygous factor H deficiency
Emmanuel Gonzales, Tim Ulinski, Dalila Habes, et al.
FEBS Letters
|
June 29, 2007
Rat hepatocytes express functional P2X receptors
Emmanuel Gonzales, Sylvie Prigent, Aurélie Abou-Lovergne, et al.
Orphanet Journal of Rare Diseases
|
November 19, 2021
In vitro functional rescue by ivacaftor of an ABCB11 variant involved in PFIC2 and intrahepatic cholestasis of pregnancy
Elodie Mareux, Martine Lapalus, Amel Ben-Saad, et al.
JIMD Reports
|
April 30, 2013
Mitochondrial Infantile Liver Disease due to TRMU Gene Mutations: Three New Cases
Pauline Gaignard, Emmanuel Gonzales, Oanez Ackermann, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 96) with videos related to
Sort By:
Page
of 10
Frontiers in Bioscience (Landmark Edition)
|
March 11, 2009
Liver diseases related to MDR3 (ABCB4) gene deficiency
Emmanuel Gonzales, Anne Davit-Spraul, Christiane Baussan, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 5, 2022
A Model for Early Endoscopic Detection of High-Risk Gastroesophageal Varices in Children With Biliary Atresia
Oanez Ackermann, Paul de Boissieu, Olivier Bernard, et al.
European Journal of Medical Genetics
|
May 15, 2021
Defining the natural history of rare genetic liver diseases: Lessons learned from the NAPPED initiative
Daan B E van Wessel, Emmanuel Gonzales, Bettina E Hansen, et al.
Pediatric Radiology
|
February 23, 2018
Diagnosis, treatment and outcome of hepatic venous outflow obstruction in paediatric liver transplantation: 24-year experience at a single centre
Alexis Galloux, Erika Pace, Stephanie Franchi-Abella, et al.
Molecular Genetics and Metabolism
|
August 3, 2014
Liver transcript analysis reveals aberrant splicing due to silent and intronic variations in the ABCB11 gene
Anne Davit-Spraul, Christophe Oliveira, Emmanuel Gonzales, et al.
Journal of Hepatology
|
May 22, 2012
Successful mutation-specific chaperone therapy with 4-phenylbutyrate in a child with progressive familial intrahepatic cholestasis type 2
Emmanuel Gonzales, Brigitte Grosse, Doris Cassio, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 17, 2016
Long-term successful liver-kidney transplantation in a child with atypical hemolytic uremic syndrome caused by homozygous factor H deficiency
Emmanuel Gonzales, Tim Ulinski, Dalila Habes, et al.
FEBS Letters
|
June 29, 2007
Rat hepatocytes express functional P2X receptors
Emmanuel Gonzales, Sylvie Prigent, Aurélie Abou-Lovergne, et al.
Orphanet Journal of Rare Diseases
|
November 19, 2021
In vitro functional rescue by ivacaftor of an ABCB11 variant involved in PFIC2 and intrahepatic cholestasis of pregnancy
Elodie Mareux, Martine Lapalus, Amel Ben-Saad, et al.
JIMD Reports
|
April 30, 2013
Mitochondrial Infantile Liver Disease due to TRMU Gene Mutations: Three New Cases
Pauline Gaignard, Emmanuel Gonzales, Oanez Ackermann, et al.
Page
of 10