Intrahepatic cholestasis

Journal of Pediatric Gastroenterology and Nutrition

Volumn 35, Issue SUPPL. 1, 2002, Pages

  Balistreri, William F ^a  

^a UNIVERSITY OF CINCINNATI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILE ACID;

ALAGILLE SYNDROME; BILE ACID METABOLISM; BILE FLOW; CLINICAL FEATURE; DISEASE COURSE; HEALTH CARE COST; HUMAN; INTRAHEPATIC CHOLESTASIS; LIVER BIOPSY; LIVER FUNCTION; LIVER TRANSPLANTATION; MOLECULAR GENETICS; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROGNOSIS; REVIEW; ANIMAL; BILE DUCT; CHILD; DIFFERENTIAL DIAGNOSIS; DISEASE MODEL; ECONOMICS; GENETICS; METABOLISM; PATHOLOGY; RESEARCH;

ALAGILLE SYNDROME; ANIMAL; BILE ACIDS AND SALTS; BILE DUCTS; CHILD; CHOLESTASIS, INTRAHEPATIC; DIAGNOSIS, DIFFERENTIAL; DISEASE MODELS, ANIMAL; HUMAN; RESEARCH; ANIMALS; HUMANS;

EID: 0036064540     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005176-200207001-00006     Document Type: Review

References (30)

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2. Nonsyndromic paucity of interlobular bile ducts: Clinical and laboratory findings of 10 cases
3. Nonsyndromatic paucity of interlobular bile ducts: Light and electron microscopic evaluation of sequential liver biopsies in early childhood
4. Idiopathic adulthood ductopenia; a cause of chronic cholestatic liver disease and biliary cirrhosis
5. Nonsyndromic paucity of intrahepatic bile ducts in infancy and idiopathic ductopenia in adulthood: The same syndrome?
6. Idiopathic biliary ductopenia in adults without symptoms of liver disease
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10. Segregation analysis of Alagille syndrome
11. Alagille syndrome: Family studies
12. Alagille syndrome
13. Deletions of 20p12 in Alagille syndrome: Frequency and molecular characterization
14. Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12
15. Alagille syndrome is caused by mutations in human Jaggedl, which encodes a ligand for Notch
16. Mutations in the human Jagged] gene are responsible for Alagille syndrome
17. Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy
18. Bile acid therapy in pediatric hepatobiliary disease: The role of ursodeoxycholic acid
19. Selective surgical management of progressive familial intrahepatic cholestasis (Byler's disease)
20. Molecular aspects of hepatobiliary transport
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22. Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region
23. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
24. Progressive familial intrahepatic cholestasis among the Arab population in Israel
25. Identification of a locus for progressive familial intrahepatic cholestasis (PFIC2) on chromosome 2q24
26. Hereditary recurrent cholestasis with lymphoedema: Two new families
27. Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis
28. Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease
29. Effects of ursodeoxycholate and cholate feeding on liver disease in FVB mice with a disrupted mdr2 P-glygoprotein gene
30. Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis