Disease: Progressive Familial Intrahepatic Cholestasis 1
- A case of progressive familial intrahepatic cholestasis (type 3) as an initial manifestation of cirrhosis-related gastrointestinal bleeding
- A female of progressive familial intrahepatic cholestasis type 3 caused by heterozygous mutations of ABCB4 gene and her cirrhosis improved after treatment of ursodeoxycholic acid: a case report
- A novel heterozygous deletion in ABCB4 gene in a Chinese family with intrahepatic cholestasis of pregnancy, neonatal hyperbilirubinemia, and cholelithiasis: Case reports and literature review
- A Rare Case of Progressive Familial Intrahepatic Cholestasis Type 4: A Case Report and Literature Review
- Analysis of clinical characteristic of children with progressive familial intrahepatic cholestasis type 3
- Analysis of clinical characteristic of pediatric with progressive familial intrahepatic cholestasis type 3
- Case Report: Add-on treatment with odevixibat in a new subtype of progressive familial intrahepatic cholestasis broadens the therapeutic horizon of genetic cholestasis
- Cell-based BSEP trans-inhibition: A novel, non-invasive test for diagnosis of antibody-induced BSEP deficiency
- Challenges faced in establishing a pediatric liver transplant program in a lower-middle-income country with free healthcare service
- Childhood Cholestatic Liver Diseases that Persist Into Adulthood: Lessons for the Adult Gastroenterologist
- Clinical and genetic analysis of cases of progressive familial intrahepatic cholestasis type 3
- Clinical and genetic study of ABCB4 gene-related cholestatic liver disease in China: children and adults
- 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
- Diagnosis and management of Alagille and progressive familial intrahepatic cholestasis
- Diagnostic algorithm for neonatal intrahepatic cholestasis integrating single-gene testing and next-generation sequencing in East Asia
- Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trials
- Hepatic artery vasospasm masquerading as early hepatic artery thrombosis in progressive familial intrahepatic cholestasis 3: a case report
- Identification of new correctors for traffic-defective ABCB4 variants by a high-content screening approach
- 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
- Liver Transplantation for Hepatocellular Carcinoma in Patients with Inherited Metabolic Liver Diseases: A Single-Center Analysis
- Low Gamma-Glutamyl Transferase Cholestasis in a Patient With X-Linked Myotubular Myopathy and Crohn's Disease
- Management and outcomes after liver transplantation for progressive familial intrahepatic cholestasis: A systematic review and meta-analysis
- Maralixibat in progressive familial intrahepatic cholestasis (MARCH-PFIC): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
- Modified by the Innovative Drugs and Strategies-Pattern of Selected Indications for Pediatric Liver Transplantation
- Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low-GGT intrahepatic cholestasis: Genetic diagnosis and genotype-phenotype correlation assessment
- Molecular basis of progressive familial intrahepatic cholestasis 3. A proteomics study
- Molecular Insights of Cholestasis in MDR2 Knockout Murine Liver Organoids
- Native liver survival in bile salt export pump deficiency: results of a retrospective cohort study
- Novel PLEC variants associated with infantile cholestasis
- NR1H4 disease: rapidly progressing neonatal intrahepatic cholestasis and early death
- Odevixibat (Bylvay): CADTH Reimbursement Recommendation: Indication: The treatment of pruritus in patients aged 6 months or older with progressive familial intrahepatic cholestasis
- Odevixibat as an adjunctive treatment for refractory pruritus in rare variants of cholestatic liver disease
- Odevixibat: A Review of a Bioactive Compound for the Treatment of Pruritus Approved by the FDA
- Opinion paper on the diagnosis and treatment of progressive familial intrahepatic cholestasis
- 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
- Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy
- Outcomes of pediatric liver transplantation for progressive familial intrahepatic cholestasis
- Paediatric research sets new standards for therapy in paediatric and adult cholestasis
- Parental liver transplantation for treating progressive familial intrahepatic cholestasis: Report of a rare case
- Plasma Concentration of Antifungal Agent Micafungin for Pediatric Living Donor Liver Transplantation
- Progressive Familial Intrahepatic Cholestasis
- 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
- Serum Transaminase Monitoring and Successful Treatment of ADHD With Dextroamphetamine in a Patient With Progressive Familial Intrahepatic Cholestasis Type 3: A Case Report and Literature Review
- Severe Neonatal Presentation of Progressive Familial Intrahepatic Cholestasis Type 4 in an Omani Infant
- Simultaneous total internal biliary diversion during liver transplantation for progressive familial intrahepatic cholestasis type 1: Standard of care?
- Successful Use of Bortezomib for Recurrent Progressive Familial Intrahepatic Cholestasis Type II After Liver Transplantation: A Pediatric Case with a 9-Year Follow-Up
- Surgical versus Medical Management of Progressive Familial Intrahepatic Cholestasis-Case Compilation and Review of the Literature
- The First Korean Adult Case of Progressive Familial Intrahepatic Cholestasis Type 7 with Novel <em>USP53</em> Splicing Variants by Next Generation Sequencing
- The Mutational Landscape Of Genetic Cholestatic Diseases In Pakistani Children
- The phospholipid flippase ATP8B1 is involved in the pathogenesis of Ulcerative Colitis via establishment of intestinal barrier function
- The spectrum of novel ABCB11 gene variations in children with progressive familial intrahepatic cholestasis type 2 in Pakistani cohorts
- Transplanting Livers in Young Children - Looking Back at 100 Cases
- Transporter Proteins as Therapeutic Drug Targets-With a Focus on SGLT2 Inhibitors
- What's new in pediatric genetic cholestatic liver disease: advances in etiology, diagnostics and therapeutic approaches
- Youngest Living Donor Liver Transplant for End-Stage Liver Disease in a 6-Month-Old With a Novel Aggressive Mutation in KIF12 Gene