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

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About: Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1995 (uk) article scientifique publié en 1995 (fr) im August 1995 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 1995 (ast) scientific article published on 01 August 1995 (en)
publication date	wds:Q59276940-970468CC-8573-4390-810E-094F390D1FBB
publication date	1995-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59276940-19C35F0E-FDBE-4268-AE27-938F56FA2D27
language of work or name	English
cites work	wds:Q59276940-0BCC4610-D30F-457D-9035-0C959D78C7CF wds:Q59276940-162C443A-5141-469A-92E8-F0B037DF83EA wds:Q59276940-18BC60CB-0CD9-441A-B62F-68F5A9FC4823 wds:Q59276940-30C77A7E-B41D-4CC6-BFD6-2F69E3242692 wds:Q59276940-46506089-50CA-4E4C-8681-6A8E9211CDF3 wds:Q59276940-67869C45-4CA9-4EC3-A0C4-890A6B9F9623 wds:Q59276940-7306ACB1-3CE2-4F0D-AA8C-0964BB776F0B wds:Q59276940-73679FE5-FC0B-4D1E-9251-700FD94BB431 wds:Q59276940-757A668B-DA4C-46BF-B95F-FAC6EAF46A45 wds:Q59276940-B6EF220B-D1C3-4AA1-8E36-5FCF04D6AB25 wds:Q59276940-D1442675-D5ED-4FDE-99EA-4B0BB3C5DDD4 wds:Q59276940-FB7B57C8-3227-4199-8412-A4A6C2B0B9D5
cites work	Temporal bone histopathologic findings in Alagille's syndrome Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2) Del(20p) with manifestations of arteriohepatic dysplasia Liver transplantation for Alagille's syndrome Arteriohepatic Dysplasia: A Benign Syndrome of Intrahepatic Cholestasis with Multiple Organ Involvement Arteriohepatic dysplasia in infancy and childhood: a longitudinal study of six patients Alagille syndrome associated with moyamoya disease Arteriohepatic dysplasia. I. Pitfalls in diagnosis and management Renal histopathology in Alagille's syndrome Long-term complications of arteriohepatic dysplasia Hepatocellular carcinoma associated with arteriohepatic dysplasia
author name string	wds:Q59276940-2D3ED5E5-4D01-4045-B884-89C87AA19397 wds:Q59276940-2E3E1705-464D-4D64-A556-CADA463B2553 wds:Q59276940-395DFA19-7D27-47EF-9B8C-CF4C22569BCE wds:Q59276940-F3F72CC3-84B3-47CC-A688-553EC56D7C92 wds:Q59276940-FD7EF784-EB83-4813-BAEA-11279BC8E51F
author name string	D J Smith A Silverman R J Sokol M R Narkewicz J M Sondheimer
rdfs:label	Outcome of syndromic paucity of interlobular bile ducts (nl) Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy (en)
skos:prefLabel	Outcome of syndromic paucity of interlobular bile ducts (nl) Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy (en)
name	Outcome of syndromic paucity of interlobular bile ducts (nl) Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy (en)
author	wds:Q59276940-7B76733C-A157-4A7D-B8C0-3F7651962563
author	Edward Hoffenberg
title	wds:Q59276940-B3193629-B9DE-4BFD-95AD-160186635DD9
title	Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy (en)
page(s)	wds:Q59276940-B3A81298-6927-490A-8948-5DDCD1AAB046
page(s)	220-224
instance of	wds:Q59276940-0F520A17-5DB3-4FE4-8868-6D903AC94318
instance of	scholarly article
main subject	wds:Q59276940-4A9931A3-5B1F-4197-AD25-70CD4FDD0A1C wds:Q59276940-A842A197-ADD5-4DE4-9920-6F1CC7A8B038
main subject	infancy stage Alagille syndrome
PubMed ID	wds:Q59276940-AD8C44EA-9D0D-4B0D-BB73-7A4B9612ADA8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7636645
PubMed ID	7636645
published in	wds:Q59276940-1BD01F65-293E-4E48-A461-9800A141A220
published in	The Journal of Pediatrics
issue	wds:Q59276940-65A3A94B-0FFE-45D2-B77D-7609411A86C8
volume	wds:Q59276940-06D19C85-1505-4F3A-B1F2-053E4E06C635
issue	2
volume	127
DOI	wds:Q59276940-A91D81BA-48A0-4FB7-BBC6-D99B778B3BAF
DOI	http://dx.doi.org/10.1016/S0022-3476(95)70298-9
DOI	10.1016/S0022-3476(95)70298-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59276940
is cites work of	Features of Alagille syndrome in 92 patients: frequency and relation to prognosis Evaluation of the pediatric patient for liver transplantation: 2014 practice guideline by the American Association for the Study of Liver Diseases, American Society of Transplantation and the North American Society for Pediatric Gastroenterology, He Notch signaling and bone remodeling Alagille syndrome Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients Heritable disorders of the bile ducts Consequences of JAG1 mutations Imaging of biliary disorders in children Early life predictive markers of liver disease outcome in an International, Multicentre Cohort of children with Alagille syndrome Outcome of liver disease in children with Alagille syndrome: a study of 163 patients THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome A longitudinal study to identify laboratory predictors of liver disease outcome in Alagille syndrome Outcome of Alagille Syndrome Patients Who Had Previously Received Kasai Operation during Infancy: A Single Center Study Alagille syndrome Clinical and pathological characteristics of Alagille syndrome in Chinese children Neonatal Cholestasis. Renal anomalies in Alagille syndrome: a disease-defining feature. Outcomes of liver transplantation for patients with Alagille syndrome: the studies of pediatric liver transplantation experience Clinical characteristics and outcome of liver transplantation for Alagille syndrome in children. Pathologic lower extremity fractures in children with Alagille syndrome Alagille syndrome in a Vietnamese cohort: mutation analysis and assessment of facial features. Italian guidelines for the management and treatment of neonatal cholestasis Alagille syndrome with cavernous carotid artery aneurysm A case of Alagille syndrome presenting with chronic cholestasis in an adult.

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