Results 111 to 120 of about 139,121 (234)
Intermediate familial intrahepatic cholestasis: phenotypic spectrum within the BRIC-PFIC spectum
In genetic hepatocellular cholestasis, among the spectrum going from benign recurrent intrahepatic cholestasis (BRIC) and profressive familial intrahepatic cholestasis, intermediate phenotypes ...
Nobili, V +8 more
core +1 more source
Purpose: To determine the outcomes of Iintrahepatic cholestasis of pregnancy and the role of postprandial serum bile acid levels in the prediction of perinatal complications.
Kudret Erkenekli +5 more
doaj
Benign recurrent intrahepatic cholestasis. A report of 26 cases.
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 ...
Benhamou, J P +2 more
core +1 more source
The association between intrahepatic cholestasis of pregnancy and neurodevelopmental conditions after excluding those with intrahepatic cholestasis of pregnancy diagnosed at delivery and after excluding those born prematurely.
Renee M. Gardner (12693008) +8 more
core +1 more source
The association between maternal intrahepatic cholestasis and different offspring neurodevelopmental conditions, stratified by the gestational period of onset of intrahepatic cholestasis.
Renee M. Gardner (12693008) +8 more
core +1 more source
Background&Aims: The mechanisms by which mutations in the familial intrahepatic cholestasis-1 gene cause Byler's disease (progressive familial intrahepatic cholestasis type :1) are unknown. Methods: Interactions among the apical sodium-dependent bile
Knisely, A S +12 more
core +1 more source
Progressive Familial Intrahepatic Cholestasis Type 1
Progressive familial intrahepatic cholestasis type 1 is a rare genetic liver disease that presents in the first year of life. Bile salts are elevated and these patients are often jaundiced.
Jansen, Peter L. M. +2 more
core +1 more source
We report a young man presenting with jaundice and severe debilitating intrahepatic cholestasis 7 months before the diagnosis of Hodgkin's lymphoma. Serum gamma-glutamyl transferase (GGT) activity was not raised.
Knisely, A S +6 more
core +1 more source
Anaesthetic considerations in progressive familial intrahepatic cholestasis (Byler's disease).
Progressive familial intrahepatic cholestasis (PFIC) or Byler's disease is one of the most common forms of intrahepatic cholestasis of metabolic and genetic origin. Affected children progress to terminal cirrhosis before adulthood and at present the only
Otte, Jean-Bernard +6 more
core +1 more source

