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

published in: Hepatology

date of publication: 1999-03-01

language: English

main subject: Alagille syndrome

Cites articles 38

Date

Title

Authors

1998-06

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

Linheng Li
1998-04-01

Guanylin stimulates regulated secretion from human neuroendocrine pancreatic cells
1997-02-01

Alagille syndrome
1997-07-01

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

Linheng Li, Amy Banta
1997-07

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Francis Collins
1997-01

Ocular Ultrasound in Alagille Syndrome
1997-09-01

Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia

Anne Joutel, Anne Ducros, Elisabeth Tournier-Lasserve
1996-05-01

10 years of pediatric liver transplantation
1996-02-01

Paucity of intrahepatic bile ducts, solitary kidney and atrophic pancreas with diabetes mellitus: atypical Alagille syndrome?
1996-03-01

Alagille's syndrome associated with cystic renal disease
1995-08-01

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

Edward Hoffenberg
1995-08-01

Liver transplantation in children with Alagille syndrome--a study of twelve cases
1995-04-14

Notch signaling
1995-01-01

Aortic calcification and renal cysts demonstrated by CT in a teenager with Alagille syndrome
1993-10-01

Survival analysis of infants under age 18 months presenting with tetralogy of Fallot
1993-03-01

Liver transplantation for Alagille's syndrome

Thomas E. Starzl, Andreas G. Tzakis
1991-08-23

TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms,TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms
1989-05-01

Alagille syndrome associated with moyamoya disease
1989-12-01

Distinct hepatic retention of Tc-99m IDA in arteriohepatic dysplasia (Alagille syndrome)
1989-11-01

Exocrine pancreatic insufficiency in syndromic paucity of interlobular bile ducts
1988-07-01

Partial external diversion of bile for the treatment of intractable pruritus associated with intrahepatic cholestasis
1988-01-01

Syndromatic paucity of interlobular bile ducts: hepatic histopathology of the early and endstage liver
1987-02-01

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases
1987-11-01

Renal abnormalities in paucity of interlobular bile ducts
1987-07-01

Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia)

Marie-Claire Gubler
1985-01-01

Management of paucity of interlobular bile ducts
1984-04-01

Arteriohepatic dysplasia: phenotypic features and family studies
1984-07-01

Possible defect in the bile secretory apparatus in arteriohepatic dysplasia (Alagille's syndrome): a review with observations on the ultrastructure of liver
1983-01-01

Arteriohepatic dysplasia. I. Pitfalls in diagnosis and management
1983-10-01

Normal organ weights of infants and children: graphs of values by age, with confidence intervals
1982-09-01

Biliary tract abnormalities in patients with arteriohepatic dysplasia
1982-05-01

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

Article - wd:Q33853650

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