Transplantation of haemochromatosis liver and intestine into a normal recipient

Gut

Volumn 45, Issue 5, 1999, Pages 783-

  Adams, Paul C ^a,c   Jeffrey, G ^a   Alanen, K ^a   Chakrabarti, S ^a   Preshaw, R ^b   Howson, W ^a   Grant, D ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

^c LONDON HEALTH SCIENCES CENTRE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; HEMOCHROMATOSIS; HOMOZYGOSITY; HUMAN; IATROGENIC DISEASE; INTESTINE TRANSPLANTATION; INTRAHEPATIC CHOLESTASIS; LIVER TRANSPLANTATION; MALE; POSTOPERATIVE COMPLICATION; PRIORITY JOURNAL; SHORT BOWEL SYNDROME;

EID: 0032694434     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.45.5.783     Document Type: Article

References (5)

1. Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis. Nat Genet 1996;13:399-408.
2. Bacon BR, Powell L, Adams PC, et al. Molecular medicine and hemochromatosis: at the crossroads. Gastroenterology 1999;116:193-207.
3. Grant D, Wall W, Mimeault R, et al. Successful small bowel-liver transplantation. Lancet 1990;335:181-4.
4. Adams PC, Chakrabarti S. Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria. Gastroenterology 1998; 114:319-23.
5. Adams PC, Ghent CN, Grant DR, et al. Transplantation of haemochromatosis liver into donor: evidence against an inherited intrahepatic defect. Gut 1991;32:1082-3.