Titlebook: Cholestatic Liver Disease; Keith D. Lindor,Jayant A. Talwalkar Book 20081st edition Humana Press 2008 autoimmune hepatitis.biopsy.liver tr

Exacting

书目名称Cholestatic Liver Disease影响因子(影响力)




书目名称Cholestatic Liver Disease影响因子(影响力)学科排名




书目名称Cholestatic Liver Disease网络公开度




书目名称Cholestatic Liver Disease网络公开度学科排名




书目名称Cholestatic Liver Disease被引频次




书目名称Cholestatic Liver Disease被引频次学科排名




书目名称Cholestatic Liver Disease年度引用




书目名称Cholestatic Liver Disease年度引用学科排名




书目名称Cholestatic Liver Disease读者反馈




书目名称Cholestatic Liver Disease读者反馈学科排名

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Primary Biliary Cirrhosis,t several lines of evidence suggest genetic and environmental factors initiate an autoimmune process. Routine laboratory testing has led to the earlier detection of disease, so patients are often asymptomatic at the time of diagnosis. Initial symptoms are usually fatigue and pruritus. Signs of decom

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Primary Sclerosing Cholangitis, It is frequently associated with inflammatory bowel disease. A typical patient with primary sclerosing cholangitis is a middle-aged male with ulcerative colitis with cholestatic liver biochemistries. The prevalence of the disease may be as high as 80–100 cases per million. Increasingly, MR cholangi

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Rare Causes of Cholestasis, cells. Molecular studies in humans have provided insight into rare cholestatic syndromes such as Alagille syndrome, progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis, and Aagenaes syndrome to name a few. Further characterization of these rare cholestatic disor

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Cholestatic Variants of Viral Disease and Alcohol,sence of viral or alcoholic hepatitis. Hepatotropic viruses, such as hepatitis A, B, C, and E, can present with an elevated alkaline phosphatase and hyperbilirubinemia. Cytomegalovirus and Epstein-Barr virus infections may also present in this manner. Alcoholic hepatitis, often defined by an AST/ALT

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Cholestatic Liver Disease Related to Systemic Disorders,review major systemic conditions that are associated with cholestasis in terms of epidemiology, pathophysiology, presentations, and possible treatment. Conditions will be discussed in terms of the likely anatomic level of involvement e.g. at the level of the canaliculus, the intralobular ductules, a

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Complications of Cholestasis, pre- and post-transplant implications. Understanding and treating these conditions can result in a significant impact on morbidity and quality of life in this group of patients. Most of what is known is based on small studies of patients with primary biliary cirrhosis (PBC) and primary sclerosing c

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2197-7399 erging insights complimented by further improvements in diag.Over the past 2 decades, there has been a steady increase in knowledge associated with the clinical manifestations of cholestatic liver disease. In addition to a growing amount of information on the well-studied disorders of primary biliar

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https://doi.org/10.1007/978-3-663-02883-3 cholestasis, benign recurrent intrahepatic cholestasis, and Aagenaes syndrome to name a few. Further characterization of these rare cholestatic disorders and the defective genes associated with them will aid in understanding hepatobiliary biology and other more common causes of intrahepatic cholestasis.