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causal role for bilirubin outside of biliary disease and pityriasis rosea ⇒ Clinicians should be aware of the increased rates of biliary pathology in people with Gilbert syndrome, while researchers should not prioritise
12 Ιουλ 2023 · We explored clinical associations with rs887829-T homozygotes (Gilbert syndrome), testing approximately 13 000 outcomes from questionnaire data, electronic health records, and anthropometric data, although we focus this paper on the healthcare coded outcomes (online supplemental table 1, figure 1).
Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine laboratory check-ups or after an intercurrent illness. The diagnosis is typically made per exclusionem, i.e. by excluding other causes of hyperbilirubinaemia.
Gilbert’s syndrome (GS) is a benign genetic disorder that is characterized by intermittent mild jaundice in which the liver doesn’t process bilirubin properly. The aim of this study was to determine whether GS patients have a different personality ...
Background and aims: Gilbert's syndrome is a common familial hyperbilirubinemia that may reduce the risk of various age-related diseases because of the antioxidant properties of bilirubin.
Background and AimsGilbert's syndrome is a common familial hyperbilirubinemia that may reduce the risk of various age-related diseases because of the antioxidant properties of bilirubin.
28 Ιαν 2024 · Abstract. Gilbert's syndrome (GS) is an extensively mild condition characterized by periods of elevated levels of bilirubin in the blood.
