Results 111 to 120 of about 139,121 (234)

Intermediate familial intrahepatic cholestasis: phenotypic spectrum within the BRIC-PFIC spectum

open access: yes, 2015
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

Are Postprandial Bile Acid Levels Helpful in Predicting Perinatal Complications in Patients with Intrahepatic Cholestasis of Pregnancy?

open access: yesÇukurova Üniversitesi Tıp Fakültesi Dergisi, 2015
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.

open access: yes, 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 ...
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.

open access: yes
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.

open access: yes
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

Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity

open access: yes, 2004
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

open access: yes, 2010
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

Polymorphisms in ABCB11 and ATP8B1 Associated with Development of Severe Intrahepatic Cholestasis in Hodgkin's Lymphoma

open access: yes, 2013
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).

open access: yes, 1995
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

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