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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書目名稱Biomarkers in Liver Disease影響因子(影響力)




書目名稱Biomarkers in Liver Disease影響因子(影響力)學科排名




書目名稱Biomarkers in Liver Disease網絡公開度




書目名稱Biomarkers in Liver Disease網絡公開度學科排名




書目名稱Biomarkers in Liver Disease被引頻次




書目名稱Biomarkers in Liver Disease被引頻次學科排名




書目名稱Biomarkers in Liver Disease年度引用




書目名稱Biomarkers in Liver Disease年度引用學科排名




書目名稱Biomarkers in Liver Disease讀者反饋




書目名稱Biomarkers in Liver Disease讀者反饋學科排名

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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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