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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
5
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pubmed:dateCreated |
2010-10-4
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pubmed:abstractText |
PFIC2 is caused by mutations in ABCB11 encoding BSEP. In most cases affected children need liver transplantation that is thought to be curative. We report on two patients who developed recurrent normal GGT cholestasis mimicking primary BSEP disease, after liver transplantation.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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|
pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0168-8278
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2010 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
981-6
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pubmed:meshHeading |
pubmed-meshheading:20800306-ATP-Binding Cassette Transporters,
pubmed-meshheading:20800306-Blotting, Western,
pubmed-meshheading:20800306-Child, Preschool,
pubmed-meshheading:20800306-Cholestasis, Intrahepatic,
pubmed-meshheading:20800306-Female,
pubmed-meshheading:20800306-Fluorescent Antibody Technique,
pubmed-meshheading:20800306-Humans,
pubmed-meshheading:20800306-Infant,
pubmed-meshheading:20800306-Liver,
pubmed-meshheading:20800306-Liver Transplantation,
pubmed-meshheading:20800306-Male,
pubmed-meshheading:20800306-Mutation,
pubmed-meshheading:20800306-Recurrence
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|
pubmed:year |
2010
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|
pubmed:articleTitle |
Relapsing features of bile salt export pump deficiency after liver transplantation in two patients with progressive familial intrahepatic cholestasis type 2.
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pubmed:affiliation |
Department of Pediatrics, Division of Gastroenterology and Hepatology, University Hospital Santa Chiara, Pisa, Italy.
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pubmed:publicationType |
Journal Article,
Case Reports
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