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About 505 results

ALLMedicine Unconjugated Hyperbilirubinemia Center

Research & Reviews  251 results

Prediction of the need for phototherapy during hospital stay in preterm infants by tran...
https://doi.org/10.1016/j.earlhumdev.2020.105029
Early Human Development; Raba AA, O'Sullivan A et. al.

May 22nd, 2020 - Neonatal hyperbilirubinemia is a common condition that frequently requires treatment with phototherapy and less commonly by exchange transfusion, especially in preterm infants. It is important to identify and monitor infants at risk of severe unco...

Induction of fecal cholesterol excretion is not effective for the treatment of hyperbil...
https://doi.org/10.1038/s41390-020-0926-2
Pediatric Research; Blankestijn M, van de Peppel IP et. al.

May 1st, 2020 - Unconjugated hyperbilirubinemia, a feature of neonatal jaundice or Crigler-Najjar syndrome, can lead to neurotoxicity and even death. We previously demonstrated that unconjugated bilirubin (UCB) can be eliminated via transintestinal excretion in G...

Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035016
Medicine Kang LL, Ma YJ et. al.

Feb 12th, 2020 - Mild hemolysis is difficult to determinate by traditional methods, and its role in Gilbert's syndrome (GS) is unclear. The main aims were to inspect the erythrocyte (RBC) survival in GS by using Levitt's carbon monoxide (CO) breath test and to ass...

Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933057
Annals of Laboratory Medicine; Kim JJ, Oh J et. al.

Dec 20th, 2019 - Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.|2019|Kim JJ,Oh J,Kim Y,Lee KA,|genetics,genetics,diagnosis,genetics,

Disease burden of Crigler-Najjar syndrome: Systematic review and future perspectives.
https://doi.org/10.1111/jgh.14853
Journal of Gastroenterology and Hepatology References; Dhawan A, Lawlor MW et. al.

Sep 9th, 2019 - Crigler-Najjar syndrome (CNS) results from biallelic mutations of UGT1A1 causing partial or total loss of uridine 5'-diphosphate glucuronyltransferase activity leading to unconjugated hyperbilirubinemia and its attendant risk for irreversible neur...

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Clinicaltrials.gov  253 results

Prediction of the need for phototherapy during hospital stay in preterm infants by tran...
https://doi.org/10.1016/j.earlhumdev.2020.105029
Early Human Development; Raba AA, O'Sullivan A et. al.

May 22nd, 2020 - Neonatal hyperbilirubinemia is a common condition that frequently requires treatment with phototherapy and less commonly by exchange transfusion, especially in preterm infants. It is important to identify and monitor infants at risk of severe unco...

Induction of fecal cholesterol excretion is not effective for the treatment of hyperbil...
https://doi.org/10.1038/s41390-020-0926-2
Pediatric Research; Blankestijn M, van de Peppel IP et. al.

May 1st, 2020 - Unconjugated hyperbilirubinemia, a feature of neonatal jaundice or Crigler-Najjar syndrome, can lead to neurotoxicity and even death. We previously demonstrated that unconjugated bilirubin (UCB) can be eliminated via transintestinal excretion in G...

Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035016
Medicine Kang LL, Ma YJ et. al.

Feb 12th, 2020 - Mild hemolysis is difficult to determinate by traditional methods, and its role in Gilbert's syndrome (GS) is unclear. The main aims were to inspect the erythrocyte (RBC) survival in GS by using Levitt's carbon monoxide (CO) breath test and to ass...

Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933057
Annals of Laboratory Medicine; Kim JJ, Oh J et. al.

Dec 20th, 2019 - Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.|2019|Kim JJ,Oh J,Kim Y,Lee KA,|genetics,genetics,diagnosis,genetics,

Disease burden of Crigler-Najjar syndrome: Systematic review and future perspectives.
https://doi.org/10.1111/jgh.14853
Journal of Gastroenterology and Hepatology References; Dhawan A, Lawlor MW et. al.

Sep 9th, 2019 - Crigler-Najjar syndrome (CNS) results from biallelic mutations of UGT1A1 causing partial or total loss of uridine 5'-diphosphate glucuronyltransferase activity leading to unconjugated hyperbilirubinemia and its attendant risk for irreversible neur...

see more →

News  1 results

Coexisting Gilbert's Syndrome and Sickle Cell Disease
https://www.medscape.com/viewarticle/444343

Abstract and Introduction We report the coexistence of Gilbert's syndrome and homozygous sickle cell disease in a child with persistent unconjugated hyperbilirubinemia. Gilbert's syndrome is a common benign hereditary disorder of bilirubin metabol...

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