Results 71 to 80 of about 105,725 (272)
Fatal intrahepatic cholestasis
A Gürgey, S Ozsoylu, N Koçak
doaj +2 more sources
A case report of vanishing bile duct syndrome after exposure to pexidartinib (PLX3397) and paclitaxel. [PDF]
Pexidartinib (PLX3397) is a small molecule tyrosine kinase and colony-stimulating factor-1 inhibitor with FDA breakthrough therapy designation for tenosynovial giant-cell tumor, and currently under study in several other tumor types, including breast ...
Chien, A Jo +5 more
core
Ursodeoxycholic acid for treatment of cholestasis in patients with hepatic amyloidosis [PDF]
Background. Amyloidosis represents a group of different diseases characterized by extracellular accumulation of pathologic fibrillar proteins in various tissues and organs.
Akoglu Bora +3 more
core +1 more source
INTRAHEPATIC CHOLESTASIS IN PREGNANCY [PDF]
<p>Abnormal liver function tests occur in 3-5% of pregnancies, with many potential causes, including coincidental liver disease (most commonly viral hepatitis or gallstones) and underlying chronic liver disease. Pruritus in pregnancy is common, affecting 23% of pregnancies, of which a small proportion will have obstetric cholestasis ...
Savić Ž. +5 more
openaire +2 more sources
Alagille syndrome (ALGS) and progressive familial intrahepatic cholestasis (PFIC) are rare, inherited cholestatic liver disorders that manifest in infants and children and are associated with impaired bile flow (ie cholestasis), pruritus and potentially ...
B. Kamath +3 more
semanticscholar +1 more source
In trophoblast cells, T/S (TNFα + SM164) activated caspase‐3, which cleaved GSDME to switch apoptosis to pyroptosis, causing cell swelling, membrane rupture, and release of LDH, HMGB1, IL‐1β and IL‐18. These cytokines induced pro‐inflammatory macrophage polarization, which in turn reinforced pyroptotic signaling in trophoblasts, amplifying systemic ...
Baoying Huang +15 more
wiley +1 more source
Benign Recurrent Intrahepatic Cholestasis: Where Are We Now?
Benign recurrent intrahepatic cholestasis (BRIC) stands as a rare genetic contributor to cholestasis, aligning itself within the spectrum of inherited intrahepatic cholestasis syndromes, such as progressive familial intrahepatic cholestasis (PFIC) and ...
Eleni V. Geladari +5 more
doaj +1 more source
Intrahepatic cholestasis of pregnancy: Case series of a rare disease in an African setting
Intrahepatic cholestasis of pregnancy commonly presents in the second and third trimester with unexplained pruritus sine materia , abnormal liver function tests, and/or elevated serum total bile acid concentration.
Davis Rubagumya +5 more
doaj +1 more source
Interventions for treating cholestasis in pregnancy (Review) [PDF]
BACKGROUND: Obstetric cholestasis has been linked to adverse maternal and fetal/neonatal outcomes. As the pathophysiology is poorly understood, therapies have been empiric.
Gurung, Vinita +5 more
core +1 more source
Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis (BRIC) is characterized by episodes of liver dysfunction called cholestasis. During these episodes, the liver cells have a reduced ability to release a digestive fluid called bile.
Alexander K. C. Leung +58 more
semanticscholar +1 more source

