(Q35561258)

8 August 2017

1 reference

title

Heritable disorders of the bile ducts (English)

1 reference

autosomal dominant polycystic kidney

8 August 2017

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14562578

autosomal recessive polycystic kidney

22 March 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14562578

22 March 2024

author name string

Binita M. Kamath

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14562578

22 March 2024

David A. Piccoli

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14562578

22 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14562578

22 March 2024

publication date

1 September 2003

1 reference

full work available at URL

8 August 2017

https://api.elsevier.com/content/article/PII:S0889855303000542?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

https://api.elsevier.com/content/article/PII:S0889855303000542?httpAccept=text/plain

22 March 2024

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

Gastroenterology Clinics of North America

22 March 2024

published in

1 reference

8 August 2017

volume

32

1 reference

8 August 2017

issue

3

1 reference

8 August 2017

page(s)

857-75, vi

1 reference

Congenital diseases of intrahepatic bile ducts: variations on the theme "ductal plate malformation"

8 August 2017

cites work

1 reference

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7 January 2021

Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft für Pädiatrische, Nephrologie

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7 January 2021

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).

1 reference

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7 January 2021

Infantile polycystic disease of the kidneys and liver: clinical, pathological and radiological correlations and comparison with congenital hepatic fibrosis

1 reference

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7 January 2021

Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease

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7 January 2021

Renal and biliary abnormalities in a new murine model of autosomal recessive polycystic kidney disease

1 reference

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7 January 2021

Biliary epithelial cells from mice with congenital polycystic kidney disease are hyperresponsive to epidermal growth factor

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7 January 2021

Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor

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7 January 2021

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

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7 January 2021

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats

1 reference

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7 January 2021

Polycystic disease of kidney and liver presenting in childhood

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7 January 2021

Diffuse renal cystic disease in children: morphologic and genetic correlations

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7 January 2021

Autosomal recessive polycystic kidney disease: long-term outcome of neonatal survivors

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7 January 2021

Latent chronic cholangitis in congenital hepatic fibrosis

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7 January 2021

Congenital hepatic fibrosis: the long-term prognosis

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7 January 2021

Polycystic disease and hepatic fibrosis in children. Renal function studies

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7 January 2021

Congenital hepatic fibrosis in children

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7 January 2021

Congenital hepatic fibrosis with gastrointestinal bleeding in early infancy

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7 January 2021

Anomalies of the intrahepatic portal venous system in congenital hepatic fibrosis

1 reference

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7 January 2021

MR cholangiography in children with autosomal recessive polycystic kidney disease

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7 January 2021

Cholangitis complicating congenital hepatic fibrosis

1 reference

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7 January 2021

Congenital hepatic fibrosis with congenital heart disease. A family study with ultrastructural features of the liver

1 reference

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7 January 2021

Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney disease

1 reference

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7 January 2021

Congenital hepatic fibrosis and cerebral aneurysm in a 32-year-old woman.

1 reference

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7 January 2021

The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8553%2803%2900054-2

7 January 2021

Polycystic kidney disease: The complete structure of the PKD1 gene and its protein

1 reference

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7 January 2021

Molecular basis of autosomal-dominant polycystic kidney disease

1 reference

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7 January 2021

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

1 reference

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7 January 2021

Evidence for a third genetic locus for autosomal dominant polycystic kidney disease

1 reference

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7 January 2021

Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur

1 reference

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7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

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7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

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7 January 2021

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis

1 reference

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7 January 2021

Outcome of liver disease in children with Alagille syndrome: a study of 163 patients

1 reference

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7 January 2021

Clinical aspects of familial cholestasis (with molecular explanations).

1 reference

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7 January 2021

Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordance

1 reference

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7 January 2021

Clinical and molecular genetics of Alagille syndrome

1 reference

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7 January 2021

Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families

1 reference

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7 January 2021

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

1 reference

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7 January 2021

Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization

1 reference

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7 January 2021

Arteriohepatic dysplasia and cardiovascular malformations

1 reference

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7 January 2021

Alagille syndrome. The widening spectrum of arteriohepatic dysplasia

1 reference

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7 January 2021

Intrahepatic "cholestasis facies": is it specific for Alagille syndrome?

1 reference

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7 January 2021

Facial features in Alagille syndrome: specific or cholestasis facies?

1 reference

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7 January 2021

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

1 reference

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7 January 2021

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

1 reference

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7 January 2021

Renovascular hypertension and vascular anomalies in Alagille syndrome

1 reference

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7 January 2021

Alagille syndrome associated with angiographic moyamoya

1 reference

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7 January 2021

Abdominal coarctation and Alagille syndrome

1 reference

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7 January 2021

Middle aortic syndrome in a boy with arteriohepatic dysplasia (Alagille syndrome).

1 reference

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7 January 2021

Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy

1 reference

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7 January 2021

Alagille syndrome with cavernous carotid artery aneurysm

1 reference

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7 January 2021

Moyamoya syndrome in children with Alagille syndrome: additional evidence of a vasculopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8553%2803%2900054-2

7 January 2021

Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8553%2803%2900054-2

7 January 2021

Liver transplantation for Alagille's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8553%2803%2900054-2

7 January 2021

Liver transplantation in children with Alagille syndrome--a study of twelve cases

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8553%2803%2900054-2

7 January 2021

Unsuspected bile duct paucity in donors for living-related liver transplantation: two case reports

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8553%2803%2900054-2

7 January 2021

The ductal plate malformation

2

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

Hepatic involvement in hereditary renal syndromes

22 March 2024

3

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

Liver changes and complications in adult polycystic kidney disease

22 March 2024

31

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

Morphometric analysis of liver lesions in cystic diseases of childhood

22 March 2024

38

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

Congenital hepatic fibrosis: evolving morphology

22 March 2024

39

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

Intracranial hemorrhages in Alagille syndrome

22 March 2024

62

1 reference

https://api.crossref.org/works/10.1016/S0889-8553(03)00054-2

22 March 2024

Identifiers

1 reference

8 August 2017

1 reference