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Titlebook: Biomarkers in Liver Disease; Victor R. Preedy Living reference work 20200th edition

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楼主: dentin
发表于 2025-3-28 18:17:32 | 显示全部楼层
Biomarkers to Monitor Graft Function Following Liver Transplantation,(albumin, bilirubin, prothrombin time). Novel genetic markers such as microRNAs also show potential as more accurate or specific biomarker for various types of injury and functions. Some of these serum biomarkers were shown to be promising in predicting disease or severity of injury when measured in
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Cortisol as Biomarkers in Cirrhosis, Child Pugh and model for end-stage liver disease scores. The diagnosis of adrenal insufficiency in cirrhosis constitutes a crucial point. Published studies have used a variety of biochemical criteria to define abnormalities in adrenal function during liver cirrhosis. Common methods used in the gene
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,Fibrinogen α-Chain as a Serum Marker of Liver Disease,have been reproduced by different laboratories, and recently a marked downregulation of this protein fragment has also been described in the initial stages of liver fibrosis. In this chapter, we have described the potential role of fibrinogen α chain and particularly the 5.9 kDa fragment of fibrinog
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Graft-Derived Cell-Free DNA as a Biomarker in Liver Transplantation,r more effective treatment intervention. It is especially helpful to guide changes in immunosuppression and to monitor immunosuppression minimization. This new approach may contribute to achieve more effective, less toxic personalized immunosuppression.
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Hydroxyproline as a Biomarker in Liver Disease, marker for diagnosis or measurement of the anti-fibrotic activity of therapeutic interventions of herbal or non-herbal medicine argues its importance as noninvasive fibrotic detecting biomarker in chronic liver diseases with severe fibrosis.
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https://doi.org/10.1007/978-3-7091-1519-0ant fibrosis. It showed promising results for predicting the presence of fibrosis in pediatric patients with NAFLD. Transient elastography, a noninvasive and objective but expensive method, showed higher performance in diagnosing significant fibrosis than APRI.
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