Recovery of graft steatosis and protein‐losing enteropathy after biliary diversion in a PFIC 1 liver transplanted child

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Pediatric Transplantation

• Publication date

  2012-08-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1111/j.1399-3046.2011.01514.xPMID 21672103
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Progressive Familial Intrahepatic Cholestasis Type 1

  2010cited by this paper
• Differences in presentation and progression between severe FIC1 and BSEP deficiencies.

  2010cited by this paper
• Partial External Biliary Diversion in Children With Progressive Familial Intrahepatic Cholestasis and Alagille Disease

  2009cited by this paper
• Liver retransplantation with external biliary diversion for progressive familial intrahepatic cholestasis type 1: A case report

  2009cited by this paper
• Allograft steatohepatitis in progressive familial intrahepatic cholestasis type 1 after living donor liver transplantation

  2009influential reference
• Liver Transplantation in Children With Progressive Familial Intrahepatic Cholestasis

  2007cited by this paper
• Liver transplantation for progressive familial intrahepatic cholestasis: Clinical and histopathological findings, outcome and impact on growth

  2007cited by this paper
• Safety of living‐related liver transplantation for progressive familial intrahepatic cholestasis

  2006cited by this paper
• Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation.

  2003cited by this paper
• Biliary diversion for progressive familial intrahepatic cholestasis: improved liver morphology and bile acid profile.

  2003cited by this paper
• Living related liver transplantation in 13 cases of progressive familial intrahepatic cholestasis.

  2003cited by this paper
• Intractable diarrhea after liver transplantation for Byler's disease: Successful treatment with bile adsorptive resin

  2002cited by this paper
• Progressive familial intrahepatic cholestasis: partial biliary diversion normalizes serum lipids and improves growth in noncirrhotic patients

  2000cited by this paper
• Genetic cholestasis syndromes.

  1999cited by this paper
• Selective surgical management of progressive familial intrahepatic cholestasis (Byler's disease).

  1995cited by this paper
• Clinical and Biochemical Findings in Progressive Familial Intrahepatic Cholestasis

  1994cited by this paper

• Post‐Transplant Metabolic Syndrome in Pediatric Liver Transplant Recipients: Definition, Prevalence and Clinical Presentation

  2025cites this paper
• SPANISH CLINICAL PRACTICE GUIDELINES FOR THE DIAGNOSIS AND MANAGEMENT OF CHOLESTATIC LIVER DISEASES IN ADULT AND PEDIATRIC POPULATION: JOINT REPORT FROM AEEH AND SEGHNP.

  2025cites this paper
• Odevixibat after liver transplant in patients with progressive familial intrahepatic cholestasis type 1: A case series

  2025cites this paper
• Internal biliary diversion using appendix during liver transplantation for progressive familial intrahepatic cholestasis type 1: A case report

  2025cites this paper
• Simultaneous total internal biliary diversion during liver transplantation for progressive familial intrahepatic cholestasis type 1: Standard of care?

  2024influential citation
• EASL Clinical Practice Guidelines on genetic cholestatic liver diseases.

  2024cites this paper
• Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trials

  2024cites this paper
• Optimal liver transplant procedure in progressive familial intrahepatic cholestasis type 1 treated with biliary diversion or intestinal transplantation: Lessons learned from three cases treated with different approaches

  2023cites this paper
• Management and outcomes after liver transplantation for progressive familial intrahepatic cholestasis: A systematic review and meta-analysis

  2023cites this paper
• Long-Term Results of Pediatric Liver Transplantation for Progressive Familial Intrahepatic Cholestasis

  2022cites this paper
• Long-Term Outcomes of Patients With Progressive Familial Intrahepatic Cholestasis After Biliary Diversion.

  2022cites this paper
• Ileal Bile Acid Transporter Inhibition Reduces Post-Transplant Diarrhea and Growth Failure in FIC1 Disease—A Case Report

  2022cites this paper
• Total Internal Biliary Diversion for Post-Liver Transplant PFIC-1-Related Allograft Injury.

  2021cites this paper
• Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency

  2021cites this paper
• Liver Transplantation in Progressive Familial Intrahepatic Cholestasis With Normal Gamma-Glutamyl Transferase: Evaluation of Post-Transplant Steatosis and Steatohepatitis

  2021cites this paper
• Recurrence of Disease After Liver Transplantation

  2021cites this paper
• Metabolic Conditions

  2021cites this paper
• Long-Term Outcome after Liver Transplantation for Progressive Familial Intrahepatic Cholestasis

  2021cites this paper
• Long‐term liver transplant outcomes for progressive familial intrahepatic cholestasis type 1: The Pittsburgh experience

  2021cites this paper
• A Report of 2 Infant Siblings with Progressive Intrahepatic Familial Cholestasis Type 1 and a Novel Homozygous Mutation in the ATP8B1 Gene Treated with Partial External Biliary Diversion and Liver Transplant

  2021influential citation
• Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency

  2021cites this paper
• Liver Steatosis and Diarrhea After Liver Transplantation for PFIC type 1: Can Biliary Diversion Solve These Problems?

  2020cites this paper
• Nasobiliary drainage prior to surgical biliary diversion in progressive familial intrahepatic cholestasis type II

  2020cites this paper
• Reversal of secondary protein‐losing enteropathy after surgical revision of a jejunal Roux‐en‐Y loop in a patient after liver transplantation

  2019cites this paper
• Next-Generation Sequencing in Paediatric Hepatology

  2019cites this paper
• Diagnostic Yield of an Algorithm for Neonatal and Infantile Cholestasis Integrating Next-Generation Sequencing.

  2019cites this paper
• Genetic Cholestatic Disorders

  2019cites this paper
• Biliary drainage as treatment for allograft steatosis following liver transplantation for PFIC‐1 disease: A single‐center experience

  2018cites this paper
• Gallengangatresie und angeborene Cholestasesyndrome

  2018cites this paper
• Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies

  2018cites this paper
• Next generation sequencing in pediatric hepatology and liver transplantation

  2018cites this paper
• Progressive Familial Intrahepatic Cholestasis.

  2018cites this paper
• Infobox 2 γ-Glutamyl-Transferase-negative progrediente familiäre intrahepatische Cholestasen ( PFIC )

  2018cites this paper
• New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical Implications

  2018cites this paper
• Intrahepatic cholestasis: Molecular physiology of bile formation and secretion

  2017cites this paper
• Genetic profiling of children with advanced cholestatic liver disease

  2017cites this paper
• Current and future therapies for inherited cholestatic liver diseases

  2017cites this paper
• Long-term challenges and perspectives of pre-adolescent liver disease.

  2017cites this paper
• Pediatric Liver Transplantation: Unique Concerns for the Critical Care Team

  2016cites this paper
• Protecting the allograft following liver transplantation for PFIC1

  2016cites this paper
• Total internal biliary diversion during liver transplantation for type 1 progressive familial intrahepatic cholestasis: a novel approach

  2016cites this paper
• Liver transplantation and the management of progressive familial intrahepatic cholestasis in children.

  2016cites this paper
• Metabolic profiles and liver steatosis in children with liver transplantation for progressive familial intrahepatic cholestasis type 1

  2015cites this paper
• Retargeting of bile salt export pump and favorable outcome in children with progressive familial intrahepatic cholestasis type 2

  2015cites this paper
• Progressive familial intrahepatic cholestasis.

  2014cites this paper
• Hepatocellular and Intrahepatic Cholestasis

  2014cites this paper
• Clinical utility gene card for: Progressive familial intrahepatic cholestasis type 1

  2013cites this paper
• Rapport d'activités 2012

  2013cites this paper
• Posttransplant metabolic syndrome in children and adolescents after liver transplantation: A systematic review

  2012cites this paper