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About 530 results

ALLMedicine™ Unconjugated Hyperbilirubinemia Center

Research & Reviews  265 results

Outcome of liver transplantation and prevalence of liver fibrosis in Crigler-Najjar syn...
https://doi.org/10.1111/ctr.14219
Clinical Transplantation; Schröder H, Junge N et. al.

Feb 5th, 2021 - Crigler-Najjar syndrome (CNS) is a rare inherited disorder that is characterized by high levels of non-hemolytic, unconjugated hyperbilirubinemia leading to brain damage and even death. Liver transplantation (LT) can correct the metabolic defect, ...

Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tun...
https://doi.org/10.1016/j.ejmg.2021.104139
European Journal of Medical Genetics; Trabelsi N, Chaouch L et. al.

Jan 9th, 2021 - Unconjugated hyperbilirubinemia (UCB) is a feature of Gilbert's syndrome (GS) and Crigler-Najjar's syndrome (CNS), which are two hereditary defects in bilirubin metabolism. Both syndromes are linked to mutations in the UGT1A1 gene, which cause eit...

The effect of ursodeoxycholic acid on indirect hyperbilirubinemia in neonates treated w...
https://doi.org/10.1080/14767058.2020.1846705
The Journal of Maternal-fetal & Neonatal Medicine : the O... Akefi R, Hashemi SM et. al.

Nov 23rd, 2020 - Indirect hyperbilirubinemia during neonatal period is a common problem, and most preterm and more than half of the term neonates find this problem. Ursodeoxycholic acid (UDCA) protects the liver against oxidative stresses and prevents cellular apo...

A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia ...
https://doi.org/10.1007/s00277-020-04176-2
Annals of Hematology; Shrestha O, Khadwal AR et. al.

Jul 17th, 2020 - Hyperbilirubinemia and pigment gallstones are frequent complications in transfusion-dependent β-thalassemia (TDβT) patients. Bilirubin production and clearance are determined by genetic as well as environmental variables like ineffective erythropo...

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Clinicaltrials.gov  265 results

Outcome of liver transplantation and prevalence of liver fibrosis in Crigler-Najjar syn...
https://doi.org/10.1111/ctr.14219
Clinical Transplantation; Schröder H, Junge N et. al.

Feb 5th, 2021 - Crigler-Najjar syndrome (CNS) is a rare inherited disorder that is characterized by high levels of non-hemolytic, unconjugated hyperbilirubinemia leading to brain damage and even death. Liver transplantation (LT) can correct the metabolic defect, ...

Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tun...
https://doi.org/10.1016/j.ejmg.2021.104139
European Journal of Medical Genetics; Trabelsi N, Chaouch L et. al.

Jan 9th, 2021 - Unconjugated hyperbilirubinemia (UCB) is a feature of Gilbert's syndrome (GS) and Crigler-Najjar's syndrome (CNS), which are two hereditary defects in bilirubin metabolism. Both syndromes are linked to mutations in the UGT1A1 gene, which cause eit...

The effect of ursodeoxycholic acid on indirect hyperbilirubinemia in neonates treated w...
https://doi.org/10.1080/14767058.2020.1846705
The Journal of Maternal-fetal & Neonatal Medicine : the O... Akefi R, Hashemi SM et. al.

Nov 23rd, 2020 - Indirect hyperbilirubinemia during neonatal period is a common problem, and most preterm and more than half of the term neonates find this problem. Ursodeoxycholic acid (UDCA) protects the liver against oxidative stresses and prevents cellular apo...

A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia ...
https://doi.org/10.1007/s00277-020-04176-2
Annals of Hematology; Shrestha O, Khadwal AR et. al.

Jul 17th, 2020 - Hyperbilirubinemia and pigment gallstones are frequent complications in transfusion-dependent β-thalassemia (TDβT) patients. Bilirubin production and clearance are determined by genetic as well as environmental variables like ineffective erythropo...

see more →