Disease: Progressive Familial Intrahepatic Cholestasis 2
- A study of exons 14, 15, and 24 of the ABCB11 gene in Egyptian children with normal GGT cholestasis
- Antisense oligonucleotides rescue an intronic splicing variant in the ABCB11 gene that causes progressive familial intrahepatic cholestasis type 2
- ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes
- Benign recurrent intrahepatic cholestasis - 2 (BRIC-2)/ABCB11 deficiency in a young child - Report from a tertiary care center in South India
- Burden of illness of progressive familial intrahepatic cholestasis in the US, UK, France, and Germany: study rationale and protocol of the PICTURE study
- Cell-based BSEP trans-inhibition: A novel, non-invasive test for diagnosis of antibody-induced BSEP deficiency
- Clinical and genetic analysis of cases of progressive familial intrahepatic cholestasis type 3
- Clinical symptoms, biochemistry, and liver histology during the native liver period of progressive familial intrahepatic cholestasis type 2
- Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases
- Comorbidity between progressive familial intrahepatic cholestasis and atopic dermatitis in a 19-month-old child
- In Vitro Rescue of the Bile Acid Transport Function of ABCB11 Variants by CFTR Potentiators
- Interim results from an ongoing, open-label, single-arm trial of odevixibat in progressive familial intrahepatic cholestasis
- Iterative antibody-induced bile salt export pump deficiency after successive liver transplantations successfully treated with plasmapheresis and rituximab
- Long-term follow-up in children with progressive familial intrahepatic cholestasis type 2 after partial external biliary diversion with focus on histopathological features
- Management and outcomes after liver transplantation for progressive familial intrahepatic cholestasis: A systematic review and meta-analysis
- Native liver survival in bile salt export pump deficiency: results of a retrospective cohort study
- Odevixibat and partial external biliary diversion showed equal improvement of cholestasis in a patient with progressive familial intrahepatic cholestasis
- Odevixibat Treatment of Alagille Syndrome: A Case Report
- 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
- Pediatric Pure Red Cell Aplasia Caused by Tacrolimus After Living-Donor Liver Transplant
- Pharmacological Premature Termination Codon Readthrough of ABCB11 in Bile Salt Export Pump Deficiency: An In Vitro Study
- Progressive Familial Intrahepatic Cholestasis
- Progressive Familial Intrahepatic Cholestasis Type 2 and Recurrence After Liver Transplantation: A Case Report
- Progressive Familial Intrahepatic Cholestasis-2 Mimicking Non-accidental Injury
- Progressive familial intrahepatic cholestasis-outcome and time to transplant after biliary diversion according to genetic subtypes
- Progressive Familial Intrahepatic Cholestasis: A Descriptive Study in a Tertiary Care Center
- Questioning Diagnostic Value of Serum Matrix Metalloproteinase 7 for Biliary Atresia
- Rescue of infant progressive familial intrahepatic cholestasis type 3 mice by repeated dosing of AAV gene therapy
- Successful Treatment with Rituximab and Immunoadsorption for an Auto-Antibody Induced Bile Salt Export Pump Deficiency in a Liver Transplanted Patient
- Surgical diversion of enterohepatic circulation in pediatric cholestasis
- Surgical versus Medical Management of Progressive Familial Intrahepatic Cholestasis-Case Compilation and Review of the Literature
- The Bile Salt Export Pump: Molecular Structure, Study Models and Small-Molecule Drugs for the Treatment of Inherited BSEP Deficiencies
- The spectrum of novel ABCB11 gene variations in children with progressive familial intrahepatic cholestasis type 2 in Pakistani cohorts
- Treatment with an ileal bile acid transporter inhibitor in patients with TJP2 deficiency