(Q52180453)

26 April 2018

review article

1 reference

title

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

1 reference

26 April 2018

1 reference

MacMillan JC

1

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26 April 2018

Shepherd R

series ordinal

2

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26 April 2018

Heritage M

series ordinal

3

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26 April 2018

publication date

1 June 1998

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26 April 2018

Bailliere's clinical gastroenterology

published in

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26 April 2018

volume

12

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26 April 2018

issue

2

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26 April 2018

page(s)

275-291

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26 April 2018

Management of paucity of interlobular bile ducts

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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

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

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The expression and function of Notch pathway genes in the developing rat eye

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7 January 2021

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

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7 January 2021

Syndromatic hepatic ductular hypoplasia (arteriohepatic dysplasia): a clinical and hepatic histologic study of three patients

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7 January 2021

Ocular anomalies in the alagille syndrome (arteriohepatic dysplasia)

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7 January 2021

Growth hormone insensitivity associated with elevated circulating growth hormone-binding protein in children with Alagille syndrome and short stature.

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7 January 2021

Del(20p) with manifestations of arteriohepatic dysplasia

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7 January 2021

Arteriohepatic dysplasia in infancy and childhood: a longitudinal study of six patients

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7 January 2021

Studies of the aetiology of neonatal hepatitis and biliary atresia

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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

Segregation analysis of Alagille syndrome

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7 January 2021

TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms

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7 January 2021

Alagille syndrome: family studies

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7 January 2021

Alagille syndrome with a spontaneous appearance of the interlobular bile ducts

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7 January 2021

Pruritus and cholestasis: therapeutic options

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7 January 2021

Lipoprotein pattern and plasma lecithin cholesterol acyl transferase activity in children with Alagille syndrome

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7 January 2021

Effect of rifampicin in the treatment of pruritus in hepatic cholestasis

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7 January 2021

Syndromatic paucity of interlobular bile ducts: hepatic histopathology of the early and endstage liver

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7 January 2021

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

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7 January 2021

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

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7 January 2021

Human ontogeny of the bile duct to portal space ratio

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7 January 2021

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

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7 January 2021

The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Antineurogenic phenotypes induced by truncated Notch proteins indicate a role in signal transduction and may point to a novel function for Notch in nuclei

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7 January 2021

Alagille's syndrome associated with cystic renal disease

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7 January 2021

Arteriohepatic dysplasia: phenotypic features and family studies

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7 January 2021

Ocular Ultrasound in Alagille Syndrome

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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

Identification and cloning of the human homolog (JAG1) of the rat Jagged1 gene from the Alagille syndrome critical region at 20p12

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7 January 2021

Fringe modulates Notch-ligand interactions.

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7 January 2021

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease

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7 January 2021

Paucity of interlobular bile ducts getting to know it better

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7 January 2021

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

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7 January 2021

Hepatocellular carcinoma in Alagille's syndrome: a family study.

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7 January 2021

Expression analysis of a Notch homologue in the mouse embryo.

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7 January 2021

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

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7 January 2021

Renal histopathology in Alagille's syndrome

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7 January 2021

Cell-cell interactions during neural development: multiple types of lateral inhibitions involved in Drosophila eye development

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7 January 2021

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

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7 January 2021

Jagged2: a serrate-like gene expressed during rat embryogenesis

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7 January 2021

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

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7 January 2021

Proto-oncogene of int-3, a mouse Notch homologue, is expressed in endothelial cells during early embryogenesis.

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7 January 2021

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

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7 January 2021

Arteriohepatic dysplasia and cardiovascular malformations

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7 January 2021

Improved neurologic function after long-term correction of vitamin E deficiency in children with chronic cholestasis

1 reference

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7 January 2021

Multicenter trial of d-alpha-tocopheryl polyethylene glycol 1000 succinate for treatment of vitamin E deficiency in children with chronic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3528%2898%2990135-X

7 January 2021

Renal abnormalities in paucity of interlobular bile ducts

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3528%2898%2990135-X

7 January 2021

Liver transplantation for Alagille's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3528%2898%2990135-X

7 January 2021

Possible defect in the bile secretory apparatus in arteriohepatic dysplasia (Alagille's syndrome): a review with observations on the ultrastructure of liver

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3528%2898%2990135-X

7 January 2021

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3528%2898%2990135-X

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0950-3528%2898%2990135-X

7 January 2021

10.1016/S0950-3528(98)90135-X

Identifiers

DOI

1 reference

26 April 2018

PubMed ID

9890073

1 reference

26 April 2018