Gilbert Syndrome Latest Advances

Genetic, clinical, and biochemical profiling of Gilbert syndrome in a Nepali cohort: High prevalence of the UGT1A1 c.-3279T>G polymorphism and correlation with hematological parameters.

Journal: PloS one

Published: January 08, 2026

Between Crigler-Najjar Syndrome Type II and Gilbert Syndrome: Expanding the Spectrum of Uridine Diphosphate Glucuronosyltransferase 1A1 (UGT1A1)-Related Hyperbilirubinemia.

Journal: Cureus

Published: December 23, 2025

Metabolic Flexibility and Exercise Performance in Adults with Gilbert's Syndrome-Associated Hyperbilirubinemia.

Journal: Sports medicine - open

Published: December 03, 2025

Prolonged Indirect Hyperbilirubinemia as a Manifestation of Postnatally Acquired Cytomegalovirus Infection.

Journal: Cureus

Published: November 30, 2025

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

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

Albumin-bilirubin score as a practical tool for prognostication in metabolic-associated steatotic liver disease.

Journal: World journal of hepatology

Published: September 07, 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

Expert Consensus on the Diagnosis and Management of Inherited Hyperbilirubinemia (2025).

Journal: Journal of clinical and translational hepatology

Published: August 26, 2025

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

Journal: Cureus

Published: August 08, 2025

Gilbert Syndrome Latest Advances

Find the Latest Research About Gilbert Syndrome

Genetic, clinical, and biochemical profiling of Gilbert syndrome in a Nepali cohort: High prevalence of the UGT1A1 c.-3279T>G polymorphism and correlation with hematological parameters.

Genetic, clinical, and biochemical profiling of Gilbert syndrome in a Nepali cohort: High prevalence of the UGT1A1 c.-3279T>G polymorphism and correlation with hematological parameters.

Between Crigler-Najjar Syndrome Type II and Gilbert Syndrome: Expanding the Spectrum of Uridine Diphosphate Glucuronosyltransferase 1A1 (UGT1A1)-Related Hyperbilirubinemia.

Between Crigler-Najjar Syndrome Type II and Gilbert Syndrome: Expanding the Spectrum of Uridine Diphosphate Glucuronosyltransferase 1A1 (UGT1A1)-Related Hyperbilirubinemia.

Metabolic Flexibility and Exercise Performance in Adults with Gilbert's Syndrome-Associated Hyperbilirubinemia.

Metabolic Flexibility and Exercise Performance in Adults with Gilbert's Syndrome-Associated Hyperbilirubinemia.

Prolonged Indirect Hyperbilirubinemia as a Manifestation of Postnatally Acquired Cytomegalovirus Infection.

Prolonged Indirect Hyperbilirubinemia as a Manifestation of Postnatally Acquired Cytomegalovirus Infection.

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.

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.

Albumin-bilirubin score as a practical tool for prognostication in metabolic-associated steatotic liver disease.

Albumin-bilirubin score as a practical tool for prognostication in metabolic-associated steatotic liver disease.

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

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

Expert Consensus on the Diagnosis and Management of Inherited Hyperbilirubinemia (2025).

Expert Consensus on the Diagnosis and Management of Inherited Hyperbilirubinemia (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.