• A Case of Dubin-Johnson Syndrome in Pregnancy
• A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts
• A case of true vocal fold jaundice
• A novel homozygous frameshift variant in the ABCC2-gene in Dubin-Johnson syndrome may predispose to chronic liver disease
• A Rare Cause of Neonatal Cholestasis Without Liver Dysfunction
• A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China
• A Time-Dependent Model Describes Methotrexate Elimination and Supports Dynamic Modification of MRP2/ABCC2 Activity
• Adult Coats' Disease, Dubin-Johnson Syndrome, and the Search for Targeted Therapies
• Autoimmune pancreatitis
• Autoimmune Pancreatitis
• Autoimmune Pancreatitis
• Autoimmune Pancreatitis
• Autoimmune Pancreatitis: A Diagnostic Challenge for the Clinician
• Autoimmune pancreatitis: An update
• Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia-A narrative review
• Case of a Young Man With Abdominal Pain and Jaundice
• Case Report: Dubin-Johnson Syndrome Presenting With Infantile Cholestasis: An Overlooked Diagnosis in an Extended Family
• Case Report: Three novel pathogenic <em>ABCC2</em> mutations identified in two patients with Dubin-Johnson syndrome
• Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin-Johnson syndrome
• Characterization of a novel ABCC2 mutation in infantile Dubin Johnson syndrome
• Clinical and pathological features of Dubin-Johnson syndrome
• Clinical and pathological features of inherited metabolic liver disease in adults
• Clinical characteristics and <em>ABCC2</em> genotype in Dubin-Johnson syndrome: A case report and review of the literature
• Clinical characteristics and ABCC2 genotype in Dubin-Johnson syndrome: A case report and review of the literature
• Clinical characteristics and follow-up of a newborn with Dubin-Johnson Syndrome: A clinical case report
• Clinical characteristics and liver profiles of Dubin-Johnson syndrome in neonates: Multicenter retrospective study
• Clinical features and ABCC2 genotypic analysis of an infant with Dubin-Johnson syndrome
• Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports
• Clinical features, concurrent disorders, and survival time in cats with suppurative cholangitis-cholangiohepatitis syndrome
• Clinical profiles and outcomes in idiopathic duct-centric chronic pancreatitis (type 2 autoimmune pancreatitis): the Mayo Clinic experience
• Clinical, Biochemical, and Molecular Characterization of Neonatal-Onset Dubin-Johnson Syndrome in a Large Case Series From the Arabs
• Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan
• Clinicobiochemical Parameters and Predictors of Liver Disease in Hospitalized Asian Indian Pregnant Women in a Tertiary Care Center in Northern India
• Common ABCB4 and ABCB11 Genotypes Are Associated with Idiopathic Chronic Cholestasis in Adults
• Concurrence of novel mutations causing Gilbert's and Dubin-Johnson syndrome with poor clinical outcomes in a Han Chinese family
• Conjugated hyperbilirubinemia after surgery. A diagnosis of Dubin-Johnson syndrome confirmed by genetic testing
• Coronary Artery Disease in Patients With Disorders of Bilirubin Excretion
• Correction to: Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report
• Development of a Pharmacokinetic Model That Accounts for the Plasma Concentrations of Conjugated and Unconjugated Bilirubin Observed in a Variety of Disease States
• Diagnosis and Management of Autoimmune Pancreatitis
• Diagnosis of a patient with Dubin-Johnson syndrome by using next generation sequencing
• Diagnostic algorithm for neonatal intrahepatic cholestasis integrating single-gene testing and next-generation sequencing in East Asia
• Diagnostic Challenges in Chronic Constrictive Pericarditis
• Diagnostic criteria and contributors to Gilbert's syndrome
• Differentiating Neonatal Dubin Johnson Syndrome from Biliary Atresia: Start Simply
• Drug-Induced Autoimmune Hepatitis: An Unusual Adverse Event of Atorvastatin Therapy
• Dubin-Johnson Syndrome
• Dubin-Johnson Syndrome
• Dubin-Johnson Syndrome
• Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report
• Dubin-Johnson syndrome as a laparoscopic finding
• Dubin-Johnson Syndrome as Differential Diagnosis for Neonatal Cholestasis
• Dubin-Johnson syndrome coexisting with glucose-6-phosphate dehydrogenase deficiency presenting after acute viral hepatitis
• Dubin-Johnson syndrome in Tunisia: Spectrum of a rare disease
• Dubin-Johnson Syndrome Presenting During Cardiac Transplantation Evaluation
• Dubin-Johnson Syndrome: A Case Report
• Epidemiology, clinical presentation, diagnosis and treatment of autoimmune pancreatitis: A retrospective analysis of 53 patients
• Excessive vincristine exposure in a child being treated for acute lymphoblastic leukaemia with underlying Dubin-Johnson syndrome: a case report
• From Pathogenesis, Clinical Manifestation, and Diagnosis to Treatment: An Overview on Autoimmune Pancreatitis
• Genetic analysis of a case with Dubin-Johnson syndrome due to two novel variants of ABCC2 gene
• Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2
• Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders
• Genotype-Phenotype Association in <em>ABCC2</em> Exon 18 Missense Mutation Leading to Dubin-Johnson Syndrome: A Case Report
• Genotype-Phenotype Association in ABCC2 Exon 18 Missense Mutation Leading to Dubin-Johnson Syndrome: A Case Report
• Hepatobiliary and Pancreatic: A black liver of Dubin-Johnson syndrome
• Histopathologic Findings in Autopsies with Emphasis on Interesting and Incidental Findings-A Pathologist's Perspective
• Hyperbilirubinemia in a Patient With Sepsis: A Diagnostic Challenge
• Identification of a compound heterozygous mutation of ABCC2 in a patient with hyperbilirubinemia
• Idiopathic Adulthood Ductopenia Causing Cirrhosis
• Idiopathic adulthood ductopenia with elevated transaminase only: A case report
• IMAGES IN CLINICAL MEDICINE. Dubin-Johnson Syndrome
• Immediate Hypersensitivity Reactions
• Immediate Hypersensitivity Reactions
• In silico screening and analysis of single-nucleotide polymorphic variants of the ABCC2 gene affecting Dubin-Johnson syndrome
• Inherited disorders of bilirubin clearance
• Laparoscopic cholecystectomy for cholecystolithiasis with Dubin-Johnson syndrome
• Literature review and report of three cases of Dubin-Johnson syndrome related to ABCC2 gene mutations in children
• Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in ABCC2 Gene
• Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing
• Mutation analysis of the <em>ABCC2</em> gene in Chinese patients with Dubin-Johnson syndrome
• Mutation analysis of the ABCC2 gene in Chinese patients with Dubin-Johnson syndrome
• Mutation spectrum and biochemical features in infants with neonatal Dubin-Johnson syndrome
• Neonatal Dubin-Johnson Syndrome and its Differentiation from Biliary Atresia
• Neonatal Dubin-Johnson syndrome: biochemical parameters, characteristics, and genetic variants study
• Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin-Johnson syndrome in a Chinese gril: A case report
• Novel compound heterozygous ABCC2 variants in patients with Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy
• Prevalence of Cerebrotendinous Xanthomatosis Among Patients Diagnosed With Acquired Juvenile-Onset Idiopathic Bilateral Cataracts
• Primary Sclerosing Cholangitis: A Concise Review of Diagnosis and Management
• Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis
• Recent Advances in Autoimmune Pancreatitis
• Relapse of Evans syndrome following BNT162b2 (Pfizer-BioNTech) COVID-19 vaccine: case report and literature review
• Rotor Syndrome
• Rotor Syndrome
• Rotor Syndrome Presenting as Dubin-Johnson Syndrome
• Structural basis for the modulation of MRP2 activity by phosphorylation and drugs
• The phenotypes and genotypes of four patients with Dubin-Johnson syndrome
• Transport mechanism of human bilirubin transporter ABCC2 tuned by the inter-module regulatory domain
• Treatment for tuberculosis in a patient with Dubin-Johnson syndrome
• Urinary coproporphyrins as a diagnostic biomarker of Dubin-Johnson syndrome in neonates: A diagnostic pathway is proposed
• Variants Associated with Infantile Cholestatic Syndromes Detected in Extrahepatic Biliary Atresia by Whole Exome Studies: A 20-Case Series from Thailand