Adult celiac disease and hemochromatosis [11]

American Journal of Gastroenterology

Volumn 95, Issue 12, 2000, Pages 3661-3662

  Turcu, Alin ^a   Lévêque, Laurent ^a   Bielefeld, Phillip ^a   Besancenot, Jean François ^a   Hillon, Patrick ^a  

^a HÔPITAL DU BOCAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOMYSIUM ANTIBODY; GLIADIN ANTIBODY; HLA DQ ANTIGEN; IMMUNOGLOBULIN A; IRON; TRANSFERRIN;

ADULT; CASE REPORT; CELIAC DISEASE; CHROMOSOME 6; DISEASE ASSOCIATION; DISEASE COURSE; FEMALE; GLUTEN FREE DIET; HEMOCHROMATOSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; IRON DEFICIENCY; LETTER; MALABSORPTION; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SIDEROSIS;

EID: 0033638587     PISSN: 00029270     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9270(00)02196-1     Document Type: Letter

References (5)

1. Precipitation of iron overload and hereditary hemochromatosis after successful treatment of celiac disease
2. Hemochromatosis and celiac sprue
3. A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis
4. Evidence for a primary association of coeliac disease to a particular DQ heterodimer
5. HLA-DR, DQ genotypes of celiac disease patients and healthy subjects from the West of Ireland