灰姑娘
发表于 2025-3-23 10:35:12
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
粘连
发表于 2025-3-23 13:53:13
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圣人
发表于 2025-3-23 21:09:43
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
发表于 2025-3-24 02:12:01
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
linear
发表于 2025-3-24 04:18:41
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
健谈
发表于 2025-3-24 07:54:24
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arrhythmic
发表于 2025-3-24 12:38:44
https://doi.org/10.1007/978-3-030-65908-0Cholangiopathies; Autoimmune cholangiopathies; Genetic cholangiopathies; Congenital biliary abnormaliti
进取心
发表于 2025-3-24 15:21:06
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hegemony
发表于 2025-3-24 19:43:25
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
addition
发表于 2025-3-24 23:38:32
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