• <em>UGT1A1</em> Variants c.864+5G&gt;T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays
• <em>UGT1A1</em>-related Bilirubin Encephalopathy/Kernicterus in Adults
• A 14-day-old boy with jaundice and apnoea
• A family study of the compound heterozygous mutation of the <em>UGT1A1</em> gene causing Crigler-Najjar syndrome type II
• A novel deletion with two pathogenic variants of UGT1A1 causing Crigler-Najjar syndrome in two unrelated Chinese
• A novel stop codon mutation in exon 1 (558C&gt;A) of the UGT1A1 gene in a Thai neonate with Crigler-Najjar syndrome type I
• A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report
• A rare case of Crigler-Najjar syndrome type 2: A case report and literature review
• AAV8 Gene Therapy for Crigler-Najjar Syndrome in Macaques Elicited Transgene T Cell Responses That Are Resident to the Liver
• ABO-incompatible Pediatric Liver Transplantation With Antibody and B-cell Depletion-free Immunosuppressive Protocol in High Consanguinity Communities
• Acute cholangitis in an old patient with Crigler-Najjar syndrome type II - a case report
• Analysis of mutation site characteristics of Gilbert syndrome and Crigler--Najjar syndrome in relation to uridine diphosphate glucuronosyltransferase A1 gene
• Auxiliary liver transplantation: a form of gene therapy in selective metabolic disorders
• Bilirubin metabolism and UDP-glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response
• Blood ACE Phenotyping for Personalized Medicine: Revelation of Patients with Conformationally Altered ACE
• Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome
• Case report: thalassemia intermedia patient with hypertension non-responsive to combined medical treatment
• Clinical outcome of hepatocyte transplantation in four pediatric patients with inherited metabolic diseases
• Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome
• Combined Spinal and TAP Blocks for Laparoscopic Cholecystectomy for a Patient with Crigler-Najjar Type 2: A Case Report
• Compound heterozygosity of a novel exon 3 frameshift (p.R357P fs*24) mutation and Y486D mutation in exon 5 of the UGT1A1 gene in a Thai infant with Crigler-Najjar syndrome type 2
• Controlled trial of phetharbital, a non-hypnotic barbiturate, in unconugated hyperbilirubinaemia
• Crigler Najjar Syndrome Type 2 (CNS Type 2): An Unwonted Cause of Jaundice in Adults
• Crigler-Najjar Syndrome Type 1: Pathophysiology, Natural History, and Therapeutic Frontier
• Crigler-Najjar syndrome type 2
• Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation
• Crigler-Najjar Syndrome Type II Diagnosed in a Patient with Jaundice Since Birth
• Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis
• Crigler-Najjar type 1 in children
• Crigler-Najjar's syndrome is a rare cause of perinatal hyperbilirubinaemia
• Determining the Minimally Effective Dose of a Clinical Candidate AAV Vector in a Mouse Model of Crigler-Najjar Syndrome
• Diagnostic criteria and contributors to Gilbert's syndrome
• Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II
• Diffusion Tensor Imaging of Auditory Pathway in Patients With Crigler-Najjar Syndrome Type I: Correlation With Auditory Brainstem Response
• Disruption of HNF1α binding site causes inherited severe unconjugated hyperbilirubinemia
• Domino liver transplantation for select metabolic disorders: Expanding the living donor pool
• Effects of high bilirubin level in pregnancy in Crigler-Najjar syndrome type 2: An extremely rare but important clinical entity to recognize
• Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population
• Genes and Pathways Promoting Long-Term Liver Repopulation by <em>Ex Vivo </em>hYAP-ERT2 Transduced Hepatocytes and Treatment of Jaundice in Gunn Rats
• Genetic analysis of a child affected with Crigler-Najjar syndrome type II
• Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects
• Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome
• Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity
• Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey
• Hepatic Parenchymal Injury in Crigler-Najjar Type I
• Hepatobiliary imaging in Crigler-Najjar syndrome type 2
• Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II
• High-throughput single-base mismatch detection for genotyping of UDP-glucuronosyltransferase (UGT1A1) with probe capture assay coupled with modified allele-specific primer extension reaction (MASPER)
• Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2
• In the rat liver, Adenoviral gene transfer efficiency is comparable to AAV
• Increased reprogramming of human fetal hepatocytes compared with adult hepatocytes in feeder-free conditions
• Indirect hyperbilirubinemia of genetic origin: Case report of Crigler-Najjar syndrome type II
• Intrathecal baclofen therapy after liver transplant in a patient with Crigler-Najjar syndrome
• Lentiviral vectors that express UGT1A1 in liver and contain miR-142 target sequences normalize hyperbilirubinemia in Gunn rats
• Linkage disequilibrium of UGT1A1 *6 and UGT1A1 *28 in relation to UGT1A6 and UGT1A7 polymorphisms
• Lipid nanoparticle-encapsulated mRNA therapy corrects serum total bilirubin level in Crigler-Najjar syndrome mouse model
• Liver after hepatocyte transplantation for liver-based metabolic disorders in children
• Liver Fibrosis Associated With Crigler-Najjar Syndrome in a Compound Heterozygote: A Case Report
• Liver histologic changes in children with type 1 of Crigler-Najjar syndrome
• Living related liver transplantation in Crigler-Najjar syndrome type 1
• Long-term reduction of jaundice in Gunn rats by nonviral liver-targeted delivery of Sleeping Beauty transposon
• Management of Crigler-Najjar syndrome
• Management of pregnancy in Crigler Najjar syndrome type 2
• Meta-analysis diagnostic accuracy of SNP-based pathogenicity detection tools: a case of UTG1A1 gene mutations
• Molecular Analysis of the UGT1A1 Gene in Korean Patients with Crigler-Najjar Syndrome Type II
• Molecular biology of glucose-6-phosphate dehydrogenase and UDP-glucuronosyltransferase 1A1 in the development of neonatal unconjugated hyperbilirubinemia
• Mutation analysis of UGT1A1 gene in patients with unconjugated hyperbilirubinemia
• New insights in bilirubin metabolism and their clinical implications
• Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia
• Orthodontic treatment of a child with Crigler-Najjar syndrome type I using tacrolimus following liver transplantation
• Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler-Najjar syndrome type I and long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
• Perioperative Management of Patient with Esophageal Carcinoma and Crigler-Najjar Syndrome Type 2: A Case Report
• Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome
• Phenobarbital in Crigler-Najjar syndrome type 1: A therapeutic option
• Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient
• Predictors of irinotecan toxicity and efficacy in treatment of metastatic colorectal cancer
• Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis
• Recommendations for pregnancies in patients with crigler-najjar syndrome
• Reduction of hyperbilirubinemia with hypericum extract (St. John's Wort) in a patient with Crigler-Najjar syndrome type II
• Response: Commentary: Case Report: Hyperbilirubinemia in Gilbert Syndrome Attenuates Covid-19-Induced Metabolic Disturbances
• Role of a homozygous A(TA)₇TAA promoter polymorphism and an exon 1 heterozygous frameshift mutation UGT1A1 in Crigler-Najjar syndrome type II in a Thai neonate
• Role of brain cytochrome P450 mono-oxygenases in bilirubin oxidation-specific induction and activity
• SARS-CoV-2 BA.2 (Omicron) variant infection in pediatric liver transplanted recipients and cohabitants during 2022 Shanghai outbreak: a prospective cohort
• Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemias
• Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II
• Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia
• Successful living donor liver transplantation plus domino-auxiliary partial orthotopic liver transplantation for pediatric patients with metabolic disorders
• Successful plasmapheresis for acute and severe unconjugated hyperbilirubinemia in a child with crigler najjar type I syndrome
• The added value of brain MR spectroscopy in children with Crigler-Najjar syndrome type-I: correlation with demographic, neurodevelopmental, and laboratory findings
• Three consecutive pregnancies in a woman with Crigler-Najjar syndrome type II with good maternal and neonatal outcomes
• Total knee arthroplasty and Crigler-Najjar syndrome: a case report
• Truncated UDP-glucuronosyltransferase (UGT) from a Crigler-Najjar syndrome type II patient colocalizes with intact UGT in the endoplasmic reticulum
• Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family
• Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases
• UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population
• UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children
• UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias
• UGT1A1 genotype in a white boy with Crigler-Najjar syndrome type 2
• Unusual Indications for a Liver Transplant: A Single-Center Experience
• Variants Associated with Infantile Cholestatic Syndromes Detected in Extrahepatic Biliary Atresia by Whole Exome Studies: A 20-Case Series from Thailand