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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
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Gastroenterology
BACKGROUND & AIMS Gut dysbiosis and myeloid-derived suppressor cells (MDSCs) are implicated in primary biliary cholangitis (PBC) pathogenesis. However, it remains unknown whether gut microbiota or their metabolites can modulate MDSCs homeostasis to ...
Rui Wang +20 more
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BACKGROUND & AIMS Gut dysbiosis and myeloid-derived suppressor cells (MDSCs) are implicated in primary biliary cholangitis (PBC) pathogenesis. However, it remains unknown whether gut microbiota or their metabolites can modulate MDSCs homeostasis to ...
Rui Wang +20 more
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.
Cynthia Levy, C. Bowlus
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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
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American Journal of Gastroenterology, 2020
OBJECTIVES In primary biliary cholangitis (PBC), bilirubin and alkaline phosphatase (ALP) are widely established as independent predictors of prognosis.
C. F. Murillo Perez +28 more
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OBJECTIVES In primary biliary cholangitis (PBC), bilirubin and alkaline phosphatase (ALP) are widely established as independent predictors of prognosis.
C. F. Murillo Perez +28 more
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Epigenetics of Primary Biliary Cholangitis
2020Primary biliary cholangitis (PBC) is a chronic cholestatic liver disease with non-suppurative destruction of the intrahepatic bile ducts. The interplay of genetics and environmental triggers contributes to the onset of the disease and subsequently results in cholestasis and progressive fibrosis.
Yikang, Li, Ruqi, Tang, Xiong, Ma
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New Treatment Paradigms in Primary Biliary Cholangitis.
Clinical Gastroenterology and Hepatology, 2023C. Levy, M. Manns, G. Hirschfield
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Medicine, 2019
Abstract Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease characterized by lymphocytic destruction of the small, intrahepatic bile ducts, causing chronic cholestasis and progressive fibrosis that eventually leads to biliary cirrhosis.
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Abstract Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease characterized by lymphocytic destruction of the small, intrahepatic bile ducts, causing chronic cholestasis and progressive fibrosis that eventually leads to biliary cirrhosis.
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Proteomics in Primary Biliary Cholangitis
2019Primary biliary cholangitis is a chronic cholestatic liver disease characterized by the presence of serum antimitochondrial antibodies and immune-mediated destruction of the small and medium-sized intrahepatic bile ducts. However, the pathophysiology of primary biliary cholangitis has not yet been completely elucidated.
You, Li +4 more
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New Therapies on the Horizon for Primary Biliary Cholangitis
Drugs, 2023Atsushi Tanaka
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