Results 101 to 110 of about 27,709 (227)
Benign recurrent intrahepatic cholestasis: late initial diagnosis in adulthood
Annals of Hepatology, 2010 Benign recurrent intrahepatic cholestasis (BRIC) is a rare autosomal recessive or sporadic disorder, characterized by recurrent episodes of intense pruritus and jaundice that resolve spontaneously without leaving considerable liver damage.
Fatih Ermis, MD +8 more
doaj +1 more source
Clinical and pathophysiological aspects of intrahepatic cholestasis of pregnancy [PDF]
, 2012 Objective: The pathogenesis of intrahepatic cholestasis of pregnancy (ICP) involves impaired bile acid and estrogen/progesterone metabolism and excretion based on genetic and environmental factors. In this thesis we evaluated different pathophysiological
Wikström Shemer, Elisabeth A
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IGFBP4 is a Metric for Primary Biliary Cholangitis and Attenuates Biliary Epithelial Cell Injury
Liver International, Volume 46, Issue 3, March 2026.ABSTRACT Background and Aims Immune‐mediated bile duct injury is the primary histological feature of autoimmune cholestatic liver diseases. Macrophages, the most abundant immune cell population in the liver, have been postulated to play a critical role in biliary repair. However, it is unclear whether activated macrophages interact with injured biliary
Xing Zhou +12 more
wiley +1 more source
The management of diagnostic uncertainty and decision-making in genetics case conferences [PDF]
, 2016 In this paper we examine one type of intraprofessional collaborative activity, namely case conferences in a specialist genetics clinic. Our specific focus is on how clinical geneticists manage decision-making through team talk in the event of diagnostic ...
Sarangi, Srikant +2 more
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An Atypical Presentation of Lemmel's Syndrome: A Rare Culprit of Intermittent Biliary Obstruction
Clinical Case Reports, Volume 14, Issue 2, February 2026.Imaging features of Lemmel syndrome illustrating intermittent extrinsic compression of the common bile duct by a periampullary duodenal diverticulum. Current CT demonstrates abrupt CBD tapering with upstream biliary dilatation, while prior imaging shows preserved ductal caliber, supporting a dynamic obstructive process.
Tinsae Anebo +6 more
wiley +1 more source
Intrahepatic cholestasis of pregnancy [PDF]
РМЖ. Мать и дитя, 2019 P.V. Kozlov1, I.V. Samsonova2 1Pirogov Russian National Research Medical University, Moscow, Russian Federation 2City Clinical Hospital No. 52, Moscow, Russian Federation Intrahepatic cholestasis of pregnancy (ICP) is a reversible form of ...
P.V. Kozlov, I.V. Samsonova
doaj
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Triplet births, particularly those achieved by assisted reproductive technologies, entail markedly elevated maternal and fetal risks, including hypertensive diseases. Intracerebral hemorrhage is an uncommon but devastating complication during the postpartum period.
Raman Goit +8 more
wiley +1 more source
Dermatoses Específicas da Gravidez [PDF]
, 2013 During pregnancy immunological, metabolic, hormonal and vascular changes occur, and can cause specific skin diseases. The specific dermatoses of pregnancy have undergone numerous changes in nomenclature and classification, partly due to advances in the ...
Coutinho, I +4 more
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Intrahepatic Cholestasis of Pregnancy Leading to Severe Vitamin K Deficiency and Coagulopathy
Case Reports in Obstetrics and Gynecology, 2017 Intrahepatic cholestasis of pregnancy is seldom associated with significant vitamin K deficiency. We report a case of a 16-year-old primigravid patient at 24 weeks and 3 days of gestation who presented with pruritus, hematuria, and preterm labor ...
Maria Maldonado +7 more
doaj +1 more source
Progressive Familial Intrahepatic Cholestasis
Clinics in Liver Disease, 2018 Genetic cholestasis has been dissected through genetic investigation. The major PFIC genes are now described. ATP8B1 encodes FIC1, ABCB11 encodes BSEP, ABCB4 encodes MDR3, TJP2 encodes TJP2, NR1H4 encodes FXR, and MYO5B encodes MYO5B. The full spectra of phenotypes associated with mutations in each gene are discussed, along with our understanding of ...
Bull, Laura N, Thompson, Richard J
openaire +4 more sources