• A family study of the compound heterozygous mutation of the <em>UGT1A1</em> gene causing Crigler-Najjar syndrome type II
• A pedigree analysis of Rotor hyperbilirubinemia combined with hepatitis B virus infection in a SLCO1B1 and SLCO1B3 gene mutations patient
• A Rare Case of Hereditary Hemochromatosis Presenting As Hyperbilirubinemia
• Acalculous Cholecystitis as a Complication of Primary Epstein-Barr Virus Infection: A Case-Based Scoping Review of the Literature
• Cardiovascular and metabolic effects of hyperbilirubinemia in a cohort of Italian Olympic athletes
• Case report: A rare case of pyruvate kinase deficiency and Crigler-Najjar syndrome type II with a novel pathogenic variant of <em>PKLR</em> and <em>UGT1A1</em> mutation
• Case report: A rare case of pyruvate kinase deficiency and Crigler-Najjar syndrome type II with a novel pathogenic variant of PKLR and UGT1A1 mutation
• Case Series: Hyperbilirubinemia under elexacaftor/tezacaftor/ivacaftor in the presence of Gilbert's syndrome
• Catastrophic Propeller Brain Injury with Large Scalp Defect Treated with Omental Flap
• Clinical and genetic definition of serum bilirubin levels for the diagnosis of Gilbert syndrome and hypobilirubinemia
• Clinical characteristics and follow-up of a newborn with Dubin-Johnson Syndrome: A clinical case report
• Clinical characteristics and genetic analysis of four children with Rotor syndrome
• Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience
• Coexistence of hereditary spherocytosis with SPTB P.Trp1150 gene variant and Gilbert syndrome: A case report and literature review
• Comment on: Brentuximab vedotin-related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?
• Correlation between the mutation spectrum of the UGT1A1 gene and clinical phenotype in patients with inherited hyperunconjugated bilirubinemia
• Crigler Najjar syndrome type II with severe jaundice as a new subtype(?) : A rare case report
• Crigler-Najjar disease: A new success for gene therapy of hereditary liver diseases
• Crigler-Najjar syndrome: looking to the future does not make us forget the present
• Development and validation of a mathematical model for evaluating shear-induced damage of von Willebrand factor
• Development of a Pharmacokinetic Model That Accounts for the Plasma Concentrations of Conjugated and Unconjugated Bilirubin Observed in a Variety of Disease States
• Development of a robust induced pluripotent stem cell atrial cardiomyocyte differentiation protocol to model atrial arrhythmia
• Diagnostic algorithm for neonatal intrahepatic cholestasis integrating single-gene testing and next-generation sequencing in East Asia
• Dubin-Johnson Syndrome
• Excessive vincristine exposure in a child being treated for acute lymphoblastic leukaemia with underlying Dubin-Johnson syndrome: a case report
• Free Bilirubin Induces Neuro-Inflammation in an Induced Pluripotent Stem Cell-Derived Cortical Organoid Model of Crigler-Najjar Syndrome
• Gene Therapy in Patients with the Crigler-Najjar Syndrome
• Genotype-Phenotype Association in <em>ABCC2</em> Exon 18 Missense Mutation Leading to Dubin-Johnson Syndrome: A Case Report
• Gilbert Syndrome
• Gilbert's syndrome in a liver transplant recipient with AIH-PBC overlap syndrome
• Gilbert's syndrome leads to elevated bilirubin after initiation of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis
• Gilbert's syndrome revisited
• H+-slip correlated to rotor free-wheeling as cause of F(1) F(O) -ATPase dysfunction in primary mitochondrial disorders
• H+-slip correlated to rotor free-wheeling as cause of F(1)F(O)-ATPase dysfunction in primary mitochondrial disorders
• H+-slip correlated to rotor free-wheeling as cause of F₁ F_O -ATPase dysfunction in primary mitochondrial disorders
• Health-related quality of life and cognitive function in children with Crigler-Najjar syndrome type 1
• Hemophagocytic Lymphohistiocytosis Secondary to Obstructive Uropathy and Escherichia coli Bacteremia
• Hereditary spherocytosis complicated by intrahepatic cholestasis: two case reports
• Homozygous SPTA1-associated hereditary pyropoikilocytosis presenting as hydrops fetalis
• Identification of a novel splice variant in SEC23B gene in a patient with concomitant presence of congenital dyserythropoietic anemia II and Gilbert's syndrome
• Incidental Scleral Icterus in an Adolescent Male With Nausea: Clinical Diagnosis of Gilbert Syndrome in the Pediatric Outpatient Setting
• Insulin-like growth factor-1 expression levels in pro-inflammatory response in calves with neonatal systemic inflammatory response syndrome
• Multiorgan Dysfunction and Associated Prognosis in Transthyretin Cardiac Amyloidosis
• Nutrition in Gilbert's Syndrome-A Systematic Review of Clinical Trials According to the PRISMA Statement
• Positive Impacts of a Four-Week Neuro-Meditation Program on Cognitive Function in Post-Acute Sequelae of COVID-19 Patients: A Randomized Controlled Trial
• Prolonged Jaundice in a Premature Breastfed Infant With Gilbert's Syndrome
• Quality Review of Prone Patient Transport Protocol
• Rotor Syndrome
• SLCO1B1 and SLCO1B3 genetic mutations in Taiwanese patients with Rotor syndrome
• Spherocytosis in Newborn Secondary to Novel Heterozygous Mutation in <em>SPTB</em> Gene: Case Report
• Successful Perioperative Management of a Patient with Gilbert Syndrome Posted for Double Valve Replacement with Tricuspid Valve Repair
• Synthetic augmentation of bilirubin metabolism in human pluripotent stem cell-derived liver organoids
• The added value of brain MR spectroscopy in children with Crigler-Najjar syndrome type-I: correlation with demographic, neurodevelopmental, and laboratory findings
• UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children
• Unconjugated Hyperbilirubinemia in Acetaminophen-Related Acute Liver Failure
• Urinary coproporphyrins as a diagnostic biomarker of Dubin-Johnson syndrome in neonates: A diagnostic pathway is proposed
• Utilizing human induced pluripotent stem cells to study atrial arrhythmias in the short QT syndrome
• What's next in gene therapy for Crigler-Najjar syndrome?