Zobrazeno 1 - 10
of 690
pro vyhledávání: '"Gilbert Syndrome"'
Publikováno v:
Journal of Inflammation Research, Vol Volume 17, Pp 5977-5983 (2024)
Yang Gou,1,2 Ping Wang,1,2 Wucheng Yang,1,2 Yimei Feng,1,2 Xiangui Peng,1,2 Hong Liu,1,2 Shuiqing Liu,1,2 Xi Zhang1,2 1Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, People’s Republic of China; 2Chongq
Externí odkaz:
https://doaj.org/article/fe651e64de214f6ea4ac553a599ec7c1
Publikováno v:
Open Life Sciences, Vol 19, Iss 1, Pp 166-9 (2024)
A congenital protein anomaly in the erythrocyte membrane skeleton causes a hereditary haemolytic illness known as hereditary spherocytosis (HS). The primary characteristic of HS is an increase in the number of tiny spherical red blood cells in the pe
Externí odkaz:
https://doaj.org/article/a6883f3e88174ff48852a647ffad5369
Publikováno v:
Nutrients, Vol 16, Iss 14, p 2247 (2024)
Gilbert syndrome is the most common hyperbilirubinemia, associated with a mutation in the UGT1A1 bilirubin gene, which produces an enzyme that conjugates bilirubin with glucuronic acid. Episodes of jaundice occurring in GS negatively affect patients
Externí odkaz:
https://doaj.org/article/f2e54c8d42164b82a6c6284e65594030
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Constant cellular damage causes a poor prognosis of hepatitis B virus (HBV) infection. Accumulating evidence indicates the cytoprotective properties of bilirubin. Here, we investigated the association of UDP glucuronosyltransferase family
Externí odkaz:
https://doaj.org/article/e4ba31bec8f547a797139007bcaa8bd8
Autor:
Aristotelis Tsiakalos, Georgios Schinas, Aggelos Karatzaferis, Emmanouil Angelos Rigopoulos, Christos Pappas, Eleni Polyzou, Effrosyni Dimopoulou, George Dimopoulos, Karolina Akinosoglou
Publikováno v:
Viruses, Vol 16, Iss 3, p 463 (2024)
Primary Epstein-Barr virus (EBV) infection manifests with diverse clinical symptoms, occasionally resulting in severe complications. This scoping review investigates the rare occurrence of acute acalculous cholecystitis (AAC) in the context of primar
Externí odkaz:
https://doaj.org/article/53bf6b532f2a4a9b9aeebc0b9f3beaac
Autor:
Radlović Vladimir, Golubović Zoran, Leković Zoran, Dučić Siniša, Radlović Nedeljko, Jovanović Branislav, Bukva Bojan, Pavićević Polina, Nikolić Dejan, Janković Jovana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 151, Iss 3-4, Pp 186-189 (2023)
Introduction/Objective. Gilbert syndrome (GS) is the most common hereditary hyperbilirubinemia. As well as mild unconjugated hyperbilirubinemia, it is characterized by the excess of bilirubin monoglucuronide over diglucuronide in the bile and thus in
Externí odkaz:
https://doaj.org/article/253d664143ce4bb0b914871622a880c3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Laura Cozzi, Federica Nuti, Irene Degrassi, Daniela Civeriati, Giulia Paolella, Gabriella Nebbia
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-5 (2022)
Abstract Background Several mutations of bilirubin uridine diphosphate-glucuronosyltransferase gene (UGT1A1) have been reported in patients with unconjugated hyperbilirubinemia. Few reports are available about the p.Pro364Leu mutation (P364L, c.1091C
Externí odkaz:
https://doaj.org/article/1d3af71e788a432c90c29396ee6f5ce8
Mild Crigler–Najjar Syndrome with Progressive Liver Disease—A Multicenter Retrospective Cohort Study
Autor:
Norman Junge, Hanna Hentschel, Dorothee Krebs-Schmitt, Amelie Stalke, Eva-Doreen Pfister, Björn Hartleben, Martin Claßen, Alexander Querfurt, Veronika Münch, Philip Bufler, Jun Oh, Enke Grabhorn
Publikováno v:
Children, Vol 10, Iss 9, p 1431 (2023)
Crigler–Najjar Syndrome (CNS) with residual activity of UDP-glucuronosyltransferase 1A1 (UGT1A1) and no need for daily phototherapy is called mild Crigler–Najjar Syndrome. Most of these patients need medical treatment for enzyme induction (phenob
Externí odkaz:
https://doaj.org/article/020f058aa8284c33b0d8290f19ed74fa
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 10614 (2023)
Bilirubin has potent biological beneficial effects, protecting against atherosclerosis, obesity, and metabolic syndrome. The aim of this study was to assess serum bilirubin concentrations and (TA)n and (GT)n microsatellite variations in the promoter
Externí odkaz:
https://doaj.org/article/1f66eec237b84abc9c3fec0b383d600d