(Q35364972)

8 August 2017

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

1 reference

8 August 2017

1 reference

Lykavieris P

1

1 reference

8 August 2017

Hadchouel M

series ordinal

2

1 reference

8 August 2017

Chardot C

series ordinal

3

1 reference

8 August 2017

Bernard O

series ordinal

4

1 reference

8 August 2017

language of work or name

English

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publication date

1 September 2001

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8 August 2017

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8 August 2017

49

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8 August 2017

3

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8 August 2017

431-435

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Variable morbidity in alagille syndrome: a review of 43 cases

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

Arteriohepatic dysplasia (Alagille syndrome; Watson-Alagille syndrome).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

Liver transplantation for Alagille's syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

Syndromic paucity of the intrahepatic bile ducts: diagnostic difficulty; severe morbidity throughout early childhood.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

Hepatocarcinoma in a child with the Alagille syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728437

Hepatocellular carcinoma associated with arteriohepatic dysplasia

12 July 2018

1 reference

12 December 2020

Hepatocellular carcinoma associated with arteriohepatic dysplasia in a 4‐year‐old girl

1 reference

12 December 2020

Long-term complications of arteriohepatic dysplasia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Arteriohepatic Dysplasia: A Benign Syndrome of Intrahepatic Cholestasis with Multiple Organ Involvement

1 reference

12 December 2020

Identifiers

DOI

10.1136/GUT.49.3.431

1 reference

8 August 2017

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8 August 2017

1 reference