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What is congenital hepatic fibrosis?
scientific article published on June 1, 1992
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
What is congenital hepatic fibrosis?
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
main subject
congenital disorder
0 references
author name string
V. J. Desmet
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1607148
retrieved
14 October 2022
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
1607148
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1607148
retrieved
14 October 2022
publication date
1 June 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
full work available at URL
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2559.1992.tb01031.x
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2559.1992.tb01031.x/fullpdf
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
published in
Histopathology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
volume
20
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
page(s)
465-477
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
cites work
Polycystic disease of kidney and liver presenting in childhood
series ordinal
15
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Localized congenital hepatic fibrosis presenting as an abdominal mass
series ordinal
19
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Infantile polycystic disease of the kidneys and liver: clinical, pathological and radiological correlations and comparison with congenital hepatic fibrosis
series ordinal
23
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Congenital hepatic fibrosis in children
series ordinal
26
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
CONGENITAL HEPATIC FIBROSIS WITH AN UNUSUAL PULMONARY LESION.
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28
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Laurence-Moon-Biedl syndrome accompanied by congenital hepatic fibrosis
series ordinal
31
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Secretory diarrhea with protein-losing enteropathy, enterocolitis cystica superficialis, intestinal lymphangiectasia, and congenital hepatic fibrosis: a new syndrome
series ordinal
33
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Polycystic kidney of autosomal dominant inheritance, polycystic liver and congenital hepatic fibrosis in a single kindred
series ordinal
35
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
"Nephronophthisis-congenital hepatic fibrosis": an additional hepatorenal disorder
series ordinal
37
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients
series ordinal
38
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Fibrosis of the liver as a congenital anomaly
series ordinal
43
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Congenital hepatic fibrosis presenting as hepatomegaly in early infancy
series ordinal
45
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
The development of the intrahepatic bile ducts in man: a keratin-immunohistochemical study
series ordinal
48
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Cell lineages and oval cell progenitors in rat liver development
series ordinal
50
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Morphological and immunohistochemical assessment of intrahepatic bile duct development in the rat.
series ordinal
52
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Cholangiopathies: past, present, and future
series ordinal
56
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Abnormalities of intrahepatic bile ducts in extrahepatic biliary atresia
series ordinal
57
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Syndromatic paucity of interlobular bile ducts: hepatic histopathology of the early and endstage liver
series ordinal
58
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Sclerosing cholangitis with neonatal onset
series ordinal
60
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Idiopathic adulthood ductopenia. A cause of chronic cholestatic liver disease and biliary cirrhosis
series ordinal
61
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Idiopathic adulthood ductopenia presenting with chronic recurrent cholestasis. A case report
series ordinal
62
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years
series ordinal
64
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Caroli disease: high-frequency US and pathologic findings
series ordinal
66
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Caroli's disease in congenital hepatic fibrosis and infantile polycystic disease
series ordinal
67
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Progressive tubulointerstitial renal disease in infancy with associated hepatic abnormalities
series ordinal
70
1 reference
stated in
Crossref
DOI
10.1111/J.1365-2559.1992.TB01031.X
reference URL
https://api.crossref.org/works/10.1111/J.1365-2559.1992.TB01031.X
retrieved
14 October 2022
Identifiers
DOI
10.1111/J.1365-2559.1992.TB01031.X
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
1607148
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1607148
retrieved
14 October 2022
PubMed publication ID
1607148
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1607148
retrieved
12 August 2017
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