Results 271 to 280 of about 4,431,933 (293)
Some of the next articles are maybe not open access.
Autoimmune Markers in Primary Biliary Cholangitis.
Clinical Liver Disease, 2023Primary biliary cholangitis (PBC) is a chronic cholestatic liver disease. The most common antibody associated with PBC is the anti-mitochondrial antibody (AMA), present in 90% to 95% of patients.
Shivani K. Shah, C. Bowlus
semanticscholar +1 more source
Medicine, 2023
PBC (formerly known as primary biliary cirrhosis and now named primary biliary cholangitis) is a disease with a wide range of severity and variable rate of progression.
G. Mells
semanticscholar +1 more source
PBC (formerly known as primary biliary cirrhosis and now named primary biliary cholangitis) is a disease with a wide range of severity and variable rate of progression.
G. Mells
semanticscholar +1 more source
Primary Biliary Cholangitis: Pathophysiology.
Clinical Liver Disease, 2023Primary biliary cholangitis (PBC) is the most common of the autoimmune liver diseases, in which there is chronic small bile duct inflammation. The pathophysiology of PBC is multifactorial, involving immune dysregulation and damage to biliary epithelial ...
I. Houri, G. Hirschfield
semanticscholar +1 more source
Primary Biliary Cholangitis: personalizing second-line therapies.
HepatologyPrimary biliary cholangitis (PBC) is an enigmatic, autoimmune disease targeting the small intralobular bile ducts resulting in cholestasis and potentially progression to biliary cirrhosis.
C. Levy, C. Bowlus
semanticscholar +1 more source
Primary Biliary Cholangitis and Primary Sclerosing Cholangitis Therapy Landscape.
American Journal of GastroenterologyPrimary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) are rare, chronic cholestatic diseases that can progress to liver failure. The goals of treatment are to halt the progression of liver disease to cirrhosis and/or liver failure ...
Sheena Bhushan +3 more
semanticscholar +1 more source
Mechanisms and molecules: What are the treatment targets for primary biliary cholangitis?
Hepatology, 2022Treatment of primary biliary cholangitis (PBC) with ursodeoxycholic acid (UDCA) is not always sufficient to prevent progression to hepatic decompensation and/or need for liver transplant.
M. Mayo
semanticscholar +1 more source
Contemporary Epidemiology of Primary Biliary Cholangitis.
Clinical Liver Disease, 2022Primary biliary cholangitis (PBC) is a cholestatic liver disease with potential evolution to liver cirrhosis when left untreated. Despite being rare, PBC has a substantial impact on the quality of life and survival of affected patients.
F. Colapietro, A. Bertazzoni, A. Lleo
semanticscholar +1 more source
Current treatment options in gastroenterology, 2022
Andrew R. Scheinberg, Cynthia Levy
semanticscholar +1 more source
Andrew R. Scheinberg, Cynthia Levy
semanticscholar +1 more source
New Therapies on the Horizon for Primary Biliary Cholangitis
Drugs, 2023Atsushi Tanaka
semanticscholar +1 more source
Factors Associated With Progression and Outcomes of Early Stage Primary Biliary Cholangitis
Clinical Gastroenterology and Hepatology, 2020George N Dalekos +2 more
exaly

