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期刊名:Clinics in liver disease

缩写:CLIN LIVER DIS

ISSN:1089-3261

e-ISSN:1557-8224

IF/分区:2.9/Q2

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共收录本刊相关文章索引1011
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Yu Jun Wong,Guan Sen Kew,Aldo J Montano-Loza Yu Jun Wong
Primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) are progressive cholestatic autoimmune liver diseases, characterized by the destruction of intrahepatic and/or extrahepatic bile ducts, leading to cirrhosis and live...
Asim Abdulhamid,Gregory J Gores,Julie K Heimbach et al. Asim Abdulhamid et al.
This clinical review details the current approach for the detection and management of perihilar cholangiocarcinoma in patients with primary sclerosing cholangitis. It summarizes the contemporary understanding of epidemiology, risk factors, ...
Kareem Khalaf,Natalia Causada Calo Kareem Khalaf
Immunoglobulin G4-related sclerosing cholangitis (IgG4-SC) is a steroid-responsive biliary manifestation of IgG4-related disease, commonly associated with type I autoimmune pancreatitis and can mimic primary SC or cholangiocarcinoma. Diagno...
Roie Tzadok,Inbal Houri Roie Tzadok
Autoimmune liver diseases, including autoimmune hepatitis, primary biliary cholangitis, and primary sclerosing cholangitis, are rare chronic conditions characterized by immune-mediated hepatobiliary injury. While traditionally viewed as dis...
Nasir Hussain,Palak J Trivedi Nasir Hussain
Sclerosing cholangitis encompasses a spectrum of disorders, characterised by multi-level biliary stricturing. The prefix 'primary' refers to the commonest form, PSC. Although rare, incidence and prevalence are rising, which when coupled wit...
Francesca Bolis,Marco Carbone Francesca Bolis
Primary biliary cholangitis (PBC) is a chronic autoimmune cholestatic liver disease characterized by persistent cholestasis and progressive fibrosis. Diagnosis relies on cholestatic biochemistry with AMA or PBC-specific antinuclear antibodi...
Shital Gandhi,Brianna Barsanti-Innes,Gisele Jolicoeur et al. Shital Gandhi et al.
Intrahepatic cholestasis of pregnancy is the most common liver disorder induced by pregnancy. It is characterized by pruritus, with onset typically at the end of the second trimester. Etiology is likely related to effects of estrogen and pr...
Eliza Flanagan,Natassia Pinpin Tan Eliza Flanagan
This article focuses on common genetic cholestatic liver syndromes, looking at genotype-phenotype correlations in conditions such as progressive familial intrahepatic cholestasis (PFIC), bile acid synthesis disorders and cholangiopathies. I...
Katie R Conover,Alyssa R Goldberg,Krupa R Mysore et al. Katie R Conover et al.
Biliary atresia is a complex cholangiopathy of infancy characterized by extrahepatic biliary obstruction and progressive intrahepatic fibroinflammatory injury. It remains the leading indication for liver transplant in children without any d...