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Titlebook: Biomarkers in Liver Disease; Vinood B. Patel,Victor R. Preedy Reference work 2017 Springer Science+Business Media Dordrecht 2017 Applicati

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发表于 2025-3-21 19:10:54 | 显示全部楼层 |阅读模式
期刊全称Biomarkers in Liver Disease
影响因子2023Vinood B. Patel,Victor R. Preedy
视频video
发行地址Embraces a holistic approach to different conditions that affect the liver and the use of biomarkers.Updates scientists and professionals on advances across the disciplines.Discusses potential applica
学科分类Biomarkers in Disease: Methods, Discoveries and Applications
图书封面Titlebook: Biomarkers in Liver Disease;  Vinood B. Patel,Victor R. Preedy Reference work 2017 Springer Science+Business Media Dordrecht 2017 Applicati
影响因子There are numerous types of liver disease that may be due to toxic agents (such as alcohol or drugs), infectious agents including viruses, congenital conditions and even poor dietary patterns. It has been suggested that there are over 100 different types.  As the consequences of liver failure can be devastating it is important that appropriate diagnosis and monitoring is carried out. Much of this characterisation entails the use of biological indicators, i.e biomarkers. .Biomarkers in Liver Disease. embraces a holistic approach by combining detailed information on different conditions that affect the liver and the use of biomarkers. Biomarkers are described in terms of conventional, new and emerging analytes, techniques, platforms and applications. It covers the latest knowledge, trends and innovations. New platforms are described which combine advances in biomedical sciences, physics, computing and chemistry.
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,The Reconstruction of Konrad Zuse’s Z3,. In addition, Hepascore is dynamic over time and has been demonstrated to predict adverse clinical outcomes in longitudinal cohorts of chronic hepatitis C and alcoholic liver disease patients. Thus, Hepascore is a valuable clinical tool to stage liver fibrosis and determine prognosis, need for trea
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,Zuse’s Computer for Binary Logic,atients with ESLD have a high risk of dying such as surgery, alcoholic hepatitis, acute liver failure, and variceal bleeding. Since the MELD score was introduced, there have been several modifications that may have increased effectiveness in certain situations. The MELD score is not an accurate biom
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https://doi.org/10.1007/978-3-531-91170-0rtal hypertension, including serum biomarkers and imaging techniques. Various serum molecules have been investigated for their ability to predict the presence of portal hypertension, some of which have showed to either correlate with the hepatic venous pressure gradient or predict clinically signifi
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https://doi.org/10.1007/978-3-531-91170-0modeling leads to a range of formation and disease-relevant degradation products of extracellular and intracellular proteins into the circulation. These fragments may provide information about the pathogenesis of disease and serve as serological biomarker targets. Clinically there is a need to ident
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https://doi.org/10.1007/978-3-531-91170-0een evaluated in liver diseases, and significant alterations have been found. Detailed understanding of the role of sialic acid, sialidases, and sialyltransferases and their interactions in liver diseases may significantly contribute to open new exciting frontiers of basic and therapeutic exploratio
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