Results 61 to 70 of about 3,364 (172)
Progressive familial intrahepatic cholestasis (PFIC) and benign recurrent intrahepatic cholestasis (BRIC) are two rare autosomal recessive disorders, characterized by cholestasis.
STRUBBE, BEATRIJS +3 more
core
Benign recurrent intrahepatic cholestasis: A long‐term follow‐up study of two patients
Two brothers with benign recurrent intrahepatic cholestasis were studied over a period of 6 years. During this period, 11 episodes of cholestasis were observed, with a mean duration of 2.6 months (range: 2 weeks to 6 months).
Kuipers, F; id_orcid +5 more
core +1 more source
A Female with Benign Recurrent Intrahepatic Cholestasis
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 any residual liver damage. Episodic attack can occur at any age but is usually seen at 2nd decade of life.
Swapan Chandra Dhar +6 more
openaire +1 more source
It is now feasible to map disease genes by screening the genome for linkage disequilibrium between the disease and marker alleles. This report presents the first application of this approach for a previously unmapped locus.
Houwen, R.H.J. (Roderick) +13 more
core +1 more source
BackgroundMutations in ATP8B1 gene were identified as a cause of low γ-glutamyltranspeptidase cholestasis with variable phenotype, ranging from Progressive Familial Intrahepatic Cholestasis to Benign Recurrent Intrahepatic Cholestasis.
Dita Cebecauerová +4 more
doaj +1 more source
Benign Recurrent Intrahepatic Cholestasis [PDF]
N J, Wareham +2 more
openaire +2 more sources
Drug-induced liver injury (DILI) is a matter of concern in the course of drug development and patient safety, often leading to discontinuation of drug-development programs or early withdrawal of drugs from market. Hepatocellular toxicity or impairment of
Vanessa Baier +7 more
doaj +1 more source
Benign recurrent intrahepatic cholestasis.
Benign recurrent intrahepatic cholestasis is a rare disorder of unknown etiology and has not yet been reported in Taiwan. We report a case with a typical clinical course. A 17-year-old Taiwanese boy had three episodes of pruritus and jaundice from February 1993 to July 1995, each lasting 3 to 4 months. Jaundice spontaneously subsided and he was symptom-
C J, Liu +6 more
openaire +1 more source

