Titlebook: Diseases of the Liver and Biliary Tree; Annarosa Floreani Book 2021 Springer Nature Switzerland AG 2021 Cholangiopathies.Autoimmune cholan

灰姑娘

Overlap Syndromesforms of PBC, PSC, and AIH, which are characterized by the presence of features of two diseases, typically PBC and AIH or PSC and AIH in the same patient. The diagnosis of OS is based on the presence or sequential development of biochemical, serological, histologic, and cholangiographic features of

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圣人

Drug-Induced Cholangiopathiesctive metabolites. Liver toxicity is a challenging issue and a frequent cause of failure during drug development. In particular, drug-induced bile duct injury is a side effect of several drugs and dietary supplements, that can be either easy to manage and characterized by a good outcome, or mostly u

champaign

Cholangiocarcinoma biliary tree. Histologically, they usually are adenocarcinomas. It is a rare cancer accounting about 3% of all gastrointestinal malignancies. Based on its anatomical location, CCA is classified as intrahepatic (iCCA), perihilar (pCCA), and distal (dCCA). Currently, the three types of CCA are consid

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Annarosa FloreaniBroadens our understanding of scientific advances in the field of biliary diseases.Provides information on the new treatments of autoimmune cholestatic liver diseases.Includes special topics like bili

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arrhythmic

https://doi.org/10.1007/978-3-030-65908-0Cholangiopathies; Autoimmune cholangiopathies; Genetic cholangiopathies; Congenital biliary abnormaliti

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hegemony

Synthesis of Therapeutic Oligonucleotidesew weeks of life with pale stools and dark urine in otherwise healthy infants. It is the end result of a destructive inflammatory process of the bile ducts, with unclear origins. BA is a condition seemingly unique to the neonatal period, characterized by obliteration of both intra and extrahepatic b

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RNA Synthesis Using the CEM Groupryogenesis of the primordial ductal plate caused by a genetically determined dysfunction of morphogenetic proteins expressed in the primary cilia of cholangiocytes (“ciliopathies”). Among this group, it is important to notice three different clusters of disease: polycystic liver diseases (PLDs), fib