(Q42112148)

16 October 2017

title

Bile-duct destruction and collagen deposition: a prominent ultrastructural feature of the liver in cystic fibrosis (English)

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16 October 2017

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Lindblad A

1

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16 October 2017

Hultcrantz R

series ordinal

2

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16 October 2017

Strandvik B

series ordinal

3

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16 October 2017

language of work or name

English

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publication date

1 August 1992

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16 October 2017

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16 October 2017

volume

16

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16 October 2017

issue

2

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16 October 2017

page(s)

372-381

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A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto

16 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Hepatobiliary disease in cystic fibrosis: a survey of current issues and concepts

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Sclerosing cholangitis in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Liver disease and common-bile-duct stenosis in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Common bile duct obstruction causing right upper abdominal pain in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Pathology of common bile duct stenosis in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Hepatic changes in young infants with cystic fibrosis: Possible relation to focal biliary cirrhosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Cystic fibrosis: its influence on the liver, biliary tree, and bile salt metabolism

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Morphological findings in the liver of children with cystic fibrosis: a light and electron microscopical study

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Prospective study of fatty acid supplementation over 3 years in patients with cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

The fatty acid composition of the serum chylomicrons and adipose tissue of children with cystic fibrosis of the pancreas

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Inspissated bile in a neonate with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Fasting serum bile acid levels in relation to liver histopathology in cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Urinary bile acid excretion in correlation to liver histopathology in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Excretion of bile acids in healthy children and children with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Hepatic lipocytes: the principal collagen-producing cells of normal rat liver

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Collagen measured in primary cultures of normal rat hepatocytes derives from lipocytes within the monolayer

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840160215

7 January 2021

Identifiers

DOI

10.1002/HEP.1840160215

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16 October 2017

1 reference