Results 121 to 130 of about 4,248 (155)

A Rare <i>ABCB5</i> Variant in a Familial Case of Intrahepatic Cholestasis of Pregnancy: A Potential Novel Genetic Contributor. [PDF]

J Clin Med
Kędzia M, Wender-Ożegowska E, Dąbrowska J, Jagodziński PP, Mostowska A.   +4 more
europepmc   +1 more source

All About Multiparametric MRI Evaluation in Biliary Tree Complications After Liver Transplant. [PDF]

Diagnostics (Basel)
Dijmărescu AD, Dumitrescu C, Nicolae CA, Enache RM, Lupescu IG.   +4 more
europepmc   +1 more source

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Benign Recurrent Intrahepatic Cholestasis

New England Journal of Medicine, 1963
INTRAHEPATIC cholestasis as a manifestation of liver disease is not an unusual finding. Such obstruction to bile flow may occur quite frequently in acute and chronic hepatitis and primary biliary c...
R H, SCHAPIRO, K J, ISSELBACHER
openaire   +4 more sources

BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS

Clinics in Liver Disease, 1999
Benign recurrent intrahepatic cholestasis is a rare autosomal recessive disorder characterized by repeated episodes of intense pruritus and jaundice. Each attack lasts from several weeks to months before resolving spontaneously. Patients are completely asymptomatic for months to years between symptomatic periods.
Velimir A, Luketic, Mitchell L, Shiffman
openaire   +3 more sources

Benign recurrent intrahepatic cholestasis

The Indian Journal of Pediatrics, 2005
Benign recurrent intrahepatic cholestasis (BRIC) is a rare cause of cholestasis in children. The disease may start in infancy or early childhood. Jaundice persists or recurs throughout life but does not lead to chronic liver disease or cirrhosis. Treatment is mostly symptomatic. The condition has not been reported in Indian children.
V, Gupta, M, Kumar, Baldev D, Bhatia
openaire   +2 more sources

Benign familial recurrent intrahepatic cholestasis

The American Journal of Digestive Diseases, 1973
Three new cases of benign familial recurrent intrahepatic cholestasis in a brother, sister, and mother are reported. These cases emphasize the familial nature of the disorder and the characteristic clinical findings of recurrent attacks, cholestatic jaundice, pruritus with increases in the serum bilirubin, and increased alkaline phosphatase.
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Familial cholestasis: Progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy

Best Practice & Research Clinical Gastroenterology, 2010
Progressive familial intrahepatic cholestasis (PFIC) type 1, 2 and 3 are due to mutations in ATP8B1, ABCB11 and ABCB4, respectively. Each of these genes encodes a hepatocanalicular transporter, which is essential for the proper formation of bile. Mutations in ABCB4 can result in progressive cholestatic disease, while mutations in ATP8B1 and ABCB11 can ...
van der Woerd, Wendy L., van Mil, Saskia W. C., Stapelbroek, Janneke M., Klomp, Leo W. J., van de Graaf, Stan F. J., Houwen, Roderick H. J.   +5 more
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Benign Recurrent Intrahepatic Cholestasis

Journal of Clinical Gastroenterology, 1989
Benign recurrent intrahepatic cholestasis is characterized by attacks of cholestasis. The purpose of our study of 26 patients was to emphasize some features uncommonly or never reported in this disease: (a) in each patient, the attacks of cholestasis were stereotypic; (b) attacks of cholestasis were not associated with pruritus in 15% of our patients; (
R, Brenard, A P, Geubel, J P, Benhamou
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Benign recurrent intrahepatic cholestasis.

The Journal of the Association of Physicians of India, 1996
When aged 25 years, a now 38-year-old man had acute hepatitis A with jaundice. In the subsequent years he had recurrent jaundice with severe itching and insomnia. Multiple hospital admissions with laparoscopy and liver biopsy failed to find a cause. On admission he was again jaundiced, but there was a discrepancy (as on previous examinations) between ...
S C, Samal, R, Kashyap, D K, Subrahmanyam, K R, Sethuraman, C, Ratnakar   +4 more
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[Benign recurrent intrahepatic cholestasis].

Orvosi hetilap, 1995
The authors report the medical history of a 19-year-old male patient, who had been admitted to the department of infectious diseases three times with recurrent icterus of unknown origin, suspected of viral hepatitis before his internal examination. The clinical picture and the histological results of liver biopsy performed in acute phase proved the ...
J, Gervain, A, Gógl, I, Kádas
openaire   +1 more source