(Q34171032)

31 July 2017

1 reference

title

Alagille syndrome. The widening spectrum of arteriohepatic dysplasia (English)

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31 July 2017

C Crosnier

1

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31 July 2017

P Lykavieris

series ordinal

2

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31 July 2017

M Meunier-Rotival

series ordinal

3

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31 July 2017

M Hadchouel

series ordinal

4

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31 July 2017

publication date

1 November 2000

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31 July 2017

published in

Clinics in liver disease

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31 July 2017

volume

4

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31 July 2017

issue

4

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31 July 2017

page(s)

765-778

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

31 July 2017

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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

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7 January 2021

Nervous and Ocular Disorders in Children with Cholestasis and Vitamin A and E Deficiencies

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7 January 2021

Alagille syndrome and deletion of 20p.

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7 January 2021

Alagille syndrome--a notch up for the Notch receptor.

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7 January 2021

Endothelial adhesion molecules in the development of the vascular tree: the garden of forking paths.

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7 January 2021

Renovascular hypertension and vascular anomalies in Alagille syndrome

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7 January 2021

Ocular anomalies in the alagille syndrome (arteriohepatic dysplasia)

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7 January 2021

Del(20p) with manifestations of arteriohepatic dysplasia

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7 January 2021

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

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7 January 2021

Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome

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7 January 2021

Abnormal lipoprotein pattern in patients with Alagille syndrome depends on Icterus severity

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7 January 2021

Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients

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7 January 2021

Screening of microdeletions of chromosome 20 in patients with Alagille syndrome

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7 January 2021

Paucity of intrahepatic bile ducts, solitary kidney and atrophic pancreas with diabetes mellitus: atypical Alagille syndrome?

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7 January 2021

Segregation analysis of Alagille syndrome

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7 January 2021

Alagille syndrome: family studies

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7 January 2021

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

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7 January 2021

Small bowel atresia, biliary atresia, and Alagille's syndrome

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7 January 2021

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

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7 January 2021

Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia)

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7 January 2021

Ocular abnormalities in Alagille syndrome

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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

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family

1 reference

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7 January 2021

Orthotopic liver transplantation reverses the adverse nutritional changes of end-stage liver disease in children

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7 January 2021

Notch signalling pathway and human diseases

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

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

1 reference

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7 January 2021

Jagged1 mutations in patients ascertained with isolated congenital heart defects

1 reference

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7 January 2021

Four generations of arteriohepatic dysplasia.

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

Alagille syndrome with interstitial 20p deletion derived from maternal ins(7;20).

1 reference

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7 January 2021

The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndrome

1 reference

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7 January 2021

Hepatic jagged1 expression studies.

1 reference

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7 January 2021

Alagille's syndrome associated with cystic renal disease

1 reference

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7 January 2021

Arteriohepatic dysplasia: phenotypic features and family studies

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Ocular Ultrasound in Alagille Syndrome

1 reference

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7 January 2021

Identification and Cloning of the Human Homolog (JAG1) of the RatJagged1Gene from the Alagille Syndrome Critical Region at 20p12

1 reference

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7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Temporal bone histopathologic findings in Alagille's syndrome

1 reference

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7 January 2021

Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome

1 reference

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7 January 2021

Jagged-1 mutation analysis in Italian Alagille syndrome patients

1 reference

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7 January 2021

Construction of an integrated physical and gene map of human chromosome 20p12 providing candidate genes for Alagille syndrome

1 reference

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7 January 2021

Aortic calcification and renal cysts demonstrated by CT in a teenager with Alagille syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Anterior segment and retinal pigmentary abnormalities in arteriohepatic dysplasia

1 reference

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7 January 2021

Variable morbidity in alagille syndrome: a review of 43 cases

1 reference

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7 January 2021

Alagille syndrome associated with moyamoya disease

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Arteriohepatic dysplasia: radiologic features of a new syndrome

1 reference

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7 January 2021

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Long-term complications of arteriohepatic dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Alagille syndrome with de Novo del(20) (p 11.2)

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Mutational analysis of the Jagged 1 gene in Alagille syndrome families

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

An antisense oligonucleotide to the notch ligand jagged enhances fibroblast growth factor-induced angiogenesis in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS1089-3261%2805%2970140-9

7 January 2021

10.1016/S1089-3261(05)70140-9

Identifiers

DOI

1 reference

31 July 2017

1 reference