Results 241 to 250 of about 48,035 (283)

The PBC Ireland patient registry: study protocol for a national platform on primary biliary cholangitis. [PDF]

Ther Adv Rare Dis
Nesbitt G, Curley A.
europepmc   +1 more source

Use of Ursodeoxycholic Acid and Cancer Risk for Patients With Primary Biliary Cholangitis.

JAMA Netw Open
Su L, Patel PJ, Shu X.
europepmc   +1 more source

Genetic evidence supports primary biliary cholangitis as a risk factor for lacunar stroke. [PDF]

iScience
Wang M, Zhang N, Zhang L, Zhang N, Yu H.
europepmc   +1 more source

Variation in microbiome and metabolites is associated with advantageous effects of cholestyramine on primary biliary cholangitis with pruritus. [PDF]

Microbiol Spectr
Zhou Y, Ying G, Shen W, Cui Y, Xiang B, Jiang M, Bao J, Jin Q.   +7 more
europepmc   +1 more source

Correction to 'Quality Measures to Enhance the Management and Treatment of Primary Biliary Cholangitis: A Delphi Consensus Study'. [PDF]

Liver Int
europepmc   +1 more source

Primary biliary cholangitis

Lancet, The
This JAMA Insights discusses the clinical presentation, diagnosis, and treatment of primary biliary cholangitis.
Atsushi Tanaka, Atsushi Takahashi, John M Vierling   +2 more
exaly   +16 more sources

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Primary biliary cholangitis

Medicina Clínica (English Edition), 2018
Primary cholangitis (cirrhosis) is a chronic cholestatic disease with an unquestionable female predominance. It is characterised by inflammation of the small and medium size bile ducts, and can eventually progress to cirrhosis. Most patients remain asymptomatic and are diagnosed by the casual finding of an anicteric biochemical cholestasis with ...
Andrew R. Scheinberg, Cynthia Levy
  +7 more sources

Genetics of Primary Biliary Cholangitis

Clinics in Liver Disease, 2022
Primary biliary cholangitis (PBC) is a rare disease of the liver characterized by an autoimmune attack on the small bile ducts. PBC is a complex trait, meaning that a large list of genetic factors interacts with environmental agents to determine its onset.
Gerussi A., Asselta R., Invernizzi P.
openaire   +2 more sources