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Author
- Alvaro, Domenico3
- Alpini, Gianfranco2
- Benedetti, Antonio2
- de Minicis, Samuele2
- Aghemo, Alessio1
- Agostinelli, Laura1
- Baroni, Gianluca Svegliati1
- Belli, Luca Saverio1
- Bitetto, Davide1
- Brenner, David1
- Bruno, Raffaele1
- Burra, Patrizia1
- Candelaresi, Cinzia1
- Canonico, Pier Luigi1
- Caraceni, Paolo1
- Carbone, Marco1
- Ciancio, Alessia1
- Coco, Barbara1
- Craxi, Antonio1
- Floreani, Annarosa1
- Franchitto, Antonio1
- Francis, Heather1
- Gardini, Ivan1
- Gasbarrini, Antonio1
Keyword
- CCl42
- Cholangiocarcinoma2
- Cholangiocyte2
- Proliferation2
- 3β-HSD1
- 3β-hydroxysteroid dehydrogenase1
- AIC1
- Alcoholic liver disease1
- Alkaline phosphatase1
- Animal models1
- Athioacetamide1
- BDL1
- Bile duct ligation1
- Boceprevir1
- Budesonide1
- CaMKII α1
- CCA1
- CDD1
- CF1
- CFTR1
- CGRP1
- Chemotoxic agents1
- Cholangiopathies1
- Cholestatic liver diseases1
- CREB1
Reviews
6 Results
- Special ArticleOpen Access
Primary Biliary Cholangitis: advances in management and treatment of the disease
Digestive and Liver DiseaseVol. 49Issue 8p841–846Published online: May 8, 2017- Pietro Invernizzi
- Annarosa Floreani
- Marco Carbone
- Marco Marzioni
- Antonio Craxi
- Luigi Muratori
- and others
Cited in Scopus: 20Primary Biliary Cholangitis, previously known as Primary Biliary Cirrhosis, is a rare disease, which mainly affects women in their fifth to seventh decades of life. It is a chronic autoimmune disease characterized by a progressive damage of interlobular bile ducts leading to ductopenia, chronic cholestasis and bile acids retention. Even if the disease usually presents a long asymptomatic phase and a slow progression, in many patients it may progress faster toward cirrhosis and its complications. - Special Article
Common issues in the management of patients in the waiting list and after liver transplantation
Digestive and Liver DiseaseVol. 49Issue 3p241–253Published online: December 31, 2016- Patrizia Burra
- Luca Saverio Belli
- Stefano Ginanni Corradini
- Riccardo Volpes
- Marco Marzioni
- Edoardo Giannini
- and others
Cited in Scopus: 18The present document contains the recommendations of an expert panel of transplant hepatologists, appointed by the Italian Association for the Study of the Liver (AISF), on how to manage the most common aspects of liver transplantation: the topics covered include: new treatments for HCV in patients on the waiting list for liver transplantation; antiviral treatments in patients with HCV recurrence after liver transplantation; prophylaxis for HBV recurrence after liver transplantation; indications for liver transplantation in alcoholic liver disease; and Immunosuppressive therapy. - Review articleOpen Access
Triple therapy with first-generation Protease Inhibitors for patients with genotype 1 chronic hepatitis C: Recommendations of the Italian Association for the Study of the Liver (AISF)
Digestive and Liver DiseaseVol. 46Issue 1p18–24Published online: October 11, 2013- Italian Association for the Study of the Liver (AISF)
- Barbara Coco
- Paolo Caraceni
- Alessio Aghemo
- Davide Bitetto
- Raffaele Bruno
- Alessia Ciancio
- and others
- Review Board:
Cited in Scopus: 11The first-generation Protease Inhibitors Boceprevir and Telaprevir administered in triple therapy regimens with Peg-interferon alpha and Ribavirin have been proven effective in increasing the rate of Sustained Virological Response in both naive and treatment-experienced patients with chronic genotype-1 hepatitis C. However, at the individual level, the therapeutic advantage of triple therapy is highly variable and results from the combination of multiple factors related to the characteristics of patient, viral status and liver disease. - Review Article
Liver carcinogenesis: Rodent models of hepatocarcinoma and cholangiocarcinoma
Digestive and Liver DiseaseVol. 45Issue 6p450–459Published online: November 26, 2012- Samuele De Minicis
- Tatiana Kisseleva
- Heather Francis
- Gianluca Svegliati Baroni
- Antonio Benedetti
- David Brenner
- and others
Cited in Scopus: 80Hepatocellular carcinoma and cholangiocarcinoma are primary liver cancers, both represent a growing challenge for clinicians due to their increasing morbidity and mortality. In the last few years a number of in vivo models of hepatocellular carcinoma and cholangiocarcinoma have been developed. The study of these models is providing a significant contribution in unveiling the pathophysiology of primary liver malignancies. They are also fundamental tools to evaluate newly designed molecules to be tested as new potential therapeutic agents in a pre-clinical set. - Mini-Symposium
Clinical implications of novel aspects of biliary pathophysiology
Digestive and Liver DiseaseVol. 42Issue 4p238–244Published online: February 18, 2010- Marco Marzioni
- Stefania Saccomanno
- Cinzia Candelaresi
- Chiara Rychlicki
- Laura Agostinelli
- Luciano Trozzi
- and others
Cited in Scopus: 16Cholangiocytes are the epithelial cells that line the biliary tree; they are the target of chronic diseases termed cholangiopathies, which represent a daily challenge for clinicians, since definitive medical treatments are not available yet. It is generally accepted that the progression of injury in the course of cholangiopathies, and promotion and progression of cholangiocarcinoma are at least in part due to the failure of the cholangiocytes’ mechanisms of adaptation to injury. Recently, several studies on the pathophysiology of the biliary epithelium have shed some light on the mechanisms that govern cholangiocyte response to injury. - Mini-Symposium
Recent advances in the regulation of cholangiocyte proliferation and function during extrahepatic cholestasis
Digestive and Liver DiseaseVol. 42Issue 4p245–252Published online: February 15, 2010- Shannon S. Glaser
- Paolo Onori
- Candace Wise
- Fuguan Yang
- Marco Marzioni
- Domenico Alvaro
- and others
Cited in Scopus: 32Bile duct epithelial cells (i.e., cholangiocytes), which line the intrahepatic biliary epithelium, are the target cells in a number of human cholestatic liver diseases (termed cholangiopathies). Cholangiocyte proliferation and death is present in virtually all human cholangiopathies. A number of recent studies have provided insights into the key mechanisms that regulate the proliferation and function of cholangiocytes during the pathogenesis of cholestatic liver diseases. In our review, we have summarised the most important of these recent studies over the past 3 years with a focus on those performed in the animal model of extrahepatic bile duct ligation.