Výsledky vyhledávání - "hepatic ductular hypoplasia"

[Alagille syndrome in 1995. Clinical and genetic data]

Autor: Deleuze, J F, Dhorne-Pollet, Sophie, Pollet, N, Meunier-Rotival, M, Hadchouel, M

National audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e6deebc38251d4b92347ad20c71e3dfb
https://hal.inrae.fr/hal-02711912

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Le syndrome d'Alagille en 1995. Données cliniques et génétiques

Autor: J F, Deleuze, S, Dhorne-Pollet, N, Pollet, M, Meunier-Rotival, M, Hadchouel

Publikováno v: Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology
Gastroentérologie Clinique et Biologique / Research and Clinics in Hepatology and Gastroenterology, Elsevier Masson, 1995, 19 (6-7), pp.587-596
Europe PubMed Central
Gastroentérologie Clinique et Biologique
Gastroentérologie Clinique et Biologique, 1995, 19 (6-7), pp.587-96

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3a72a90d8e49e20c44ef986613338eeb
https://hal.inrae.fr/hal-02711912

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Akademický článek

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

Autor: M. Gautier, Daniel Alagille, Michel Odièvre, Dommergues Jp

Publikováno v: The Journal of pediatrics. 86(1)

Among 30 children with hepatic ductular hypoplasia and normal extrahepatic bile ducts, 15 formed a homogeneous, readily recognizable group. In addition to chronic cholestasis, they have characteristic facies, a mesosystolic murmur, vertebral arch def

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::785c26990412f6a15142d9cc0946b04b
https://pubmed.ncbi.nlm.nih.gov/803282

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Hereditary Neonatal Cholestasis Combined with Vascular Malformations

Autor: Svein Sørland, Tom Henriksen, Øystein Aagenaes

Publikováno v: Liver Diseases in Infancy and Childhood ISBN: 9789401014199

In the recent years Alagille and coworkers (3) and Watson & Miller (7) have described a condition with cholestasis and hepatic ductular hypoplasia combined with peripheral pulmonary stenosis and some other malformations of which a characteristic faci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf7f48463961f87d4eda7d41fe2c3690
https://doi.org/10.1007/978-94-010-1417-5_18

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Xanthomas in the Watson-Alagille syndrome

Autor: J.L. Burton, C.F.M. Weston

Publikováno v: Journal of the American Academy of Dermatology. 16(5 Pt 2)

The Watson-Alagille syndrome is a distinctive type of congenital cholestasis, in which hepatic ductular hypoplasia is associated with various ocular, bony, and cardiac anomalies, often with a characteristic facies. The prognosis is surprisingly good,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe8f507597a34c89905bbf66f2dc8e64
https://pubmed.ncbi.nlm.nih.gov/3108338

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Intra-Hepatic Biliary Atresia (Hepatic Ductular Hypoplasia)

Autor: Daniel Alagille

Publikováno v: Liver Diseases in Infancy and Childhood ISBN: 9789401014199

It is uncommon to discuss intrahepatic biliary atresia without extrahepatic biliary atresia. We have studied 34 children with ‘intrahepatic biliary atresia’ (5, 6). This condition has been described by many authors under different names (table 1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7f8cd7070ea96c7e9fa88b13cb2916b5
https://doi.org/10.1007/978-94-010-1417-5_11

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Hepatic ductular hypoplasia with multiple abnormalities in a newborn

Autor: C.A. Montagnani

Publikováno v: Journal of Pediatric Surgery. 15:235

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::76960bf56609569ca01ece2ecccb9a66
https://doi.org/10.1016/s0022-3468(80)80094-7

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