Disease: Rotor syndrome
- A family study of the compound heterozygous mutation of the <em>UGT1A1</em> gene causing Crigler-Najjar syndrome type II
- 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
- 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 utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience
- Comment on: Brentuximab vedotin-related neuropathy in a patient with Gilbert syndrome: Do mutations of UGT1A1 gene affect brentuximab toxicity?
- 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 F<sub>1</sub> F<sub>O</sub> -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
- 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
- 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?