Rotor Syndrome Latest Advances

Persistent Unilateral Scleral Icterus in a Patient with Gilbert Syndrome and Prior Facial Malignancy: A Case Report and Review of the Literature.

Journal: Ophthalmic plastic and reconstructive surgery

Published: November 18, 2025

Low-grade non-muscle-invasive urothelial carcinoma of the bladder in a 16-year-old boy with UGT1A1 polymorphism and Gilbert's syndrome: A case report.

Journal: Urology case reports

Published: November 02, 2025

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

Journal: Cureus

Published: October 31, 2025

p.Gly693Arg Homozygote Mutation in Dubin-Johnson Syndrome with Atypical Liver Biopsy due to Reactivation of Hepatitis B Concomitant with Persistent Loss of Kidney Function.

Journal: Acta medica Indonesiana

Published: October 06, 2025

Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile.

Journal: Fetal and pediatric pathology

Published: September 27, 2025

Effects of nonsense genetic variants on OATP1B1 expression and transport activity in vitro.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Published: September 05, 2025

Expert consensus on the diagnosis and therapy of inherited hyperbilirubinemia (version 2025)

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology

Published: August 28, 2025

When Zoonosis Meets Genetics: Brucellosis and Gilbert Syndrome in a Young Woman From Rural Nepal.

Journal: Cureus

Published: August 08, 2025

Challenges in the pathological diagnosis of erythropoietic protoporphyria: a case report.

Journal: Frontiers in medicine

Published: July 13, 2025

Serum bilirubin concentrations and their association with clinical and radiological outcomes in multiple sclerosis: A large cohort study.

Journal: Annals of hepatology

Published: July 11, 2025

Clinical and molecular genetic analysis of nine patients with neonatal Dubin-Johnson syndrome

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology

Published: June 18, 2025

Pharmacokinetics and Pharmacodynamics of Faldaprevir Following Multiple Oral Rising Doses in Healthy Volunteers and Subjects with Gilbert's Syndrome.

Journal: Clinical pharmacology in drug development

Published: May 28, 2025

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Persistent Unilateral Scleral Icterus in a Patient with Gilbert Syndrome and Prior Facial Malignancy: A Case Report and Review of the Literature.

Persistent Unilateral Scleral Icterus in a Patient with Gilbert Syndrome and Prior Facial Malignancy: A Case Report and Review of the Literature.

Low-grade non-muscle-invasive urothelial carcinoma of the bladder in a 16-year-old boy with UGT1A1 polymorphism and Gilbert's syndrome: A case report.

Low-grade non-muscle-invasive urothelial carcinoma of the bladder in a 16-year-old boy with UGT1A1 polymorphism and Gilbert's syndrome: A case report.

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

p.Gly693Arg Homozygote Mutation in Dubin-Johnson Syndrome with Atypical Liver Biopsy due to Reactivation of Hepatitis B Concomitant with Persistent Loss of Kidney Function.

p.Gly693Arg Homozygote Mutation in Dubin-Johnson Syndrome with Atypical Liver Biopsy due to Reactivation of Hepatitis B Concomitant with Persistent Loss of Kidney Function.

Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile.

Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile.

Effects of nonsense genetic variants on OATP1B1 expression and transport activity in vitro.

Effects of nonsense genetic variants on OATP1B1 expression and transport activity in vitro.

Expert consensus on the diagnosis and therapy of inherited hyperbilirubinemia (version 2025)

Expert consensus on the diagnosis and therapy of inherited hyperbilirubinemia (version 2025)

When Zoonosis Meets Genetics: Brucellosis and Gilbert Syndrome in a Young Woman From Rural Nepal.

When Zoonosis Meets Genetics: Brucellosis and Gilbert Syndrome in a Young Woman From Rural Nepal.

Challenges in the pathological diagnosis of erythropoietic protoporphyria: a case report.

Challenges in the pathological diagnosis of erythropoietic protoporphyria: a case report.

Serum bilirubin concentrations and their association with clinical and radiological outcomes in multiple sclerosis: A large cohort study.

Serum bilirubin concentrations and their association with clinical and radiological outcomes in multiple sclerosis: A large cohort study.

Clinical and molecular genetic analysis of nine patients with neonatal Dubin-Johnson syndrome

Clinical and molecular genetic analysis of nine patients with neonatal Dubin-Johnson syndrome

Pharmacokinetics and Pharmacodynamics of Faldaprevir Following Multiple Oral Rising Doses in Healthy Volunteers and Subjects with Gilbert's Syndrome.

Pharmacokinetics and Pharmacodynamics of Faldaprevir Following Multiple Oral Rising Doses in Healthy Volunteers and Subjects with Gilbert's Syndrome.