Genetic hemochromatosis and blood donation;Hémochromatose génétique et don du sang

Annales de Medecine Interne

Volumn 152, Issue 7, 2001, Pages 452-454

  Courtois, Françoise ^a   Danic, Bruno ^b  

^a Direction Médicale et Scientifique de l'EFS ^*  (France)

^b EFS Bretagne   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD DONOR; DISEASE CLASSIFICATION; GENE MUTATION; GENETIC DISORDER; GENETIC HETEROGENEITY; HEMOCHROMATOSIS; HUMAN; SHORT SURVEY;

BLOOD DONORS; BLOOD TRANSFUSION; FRANCE; HEMOCHROMATOSIS; HUMANS; PRACTICE GUIDELINES; RISK ASSESSMENT;

EID: 17944393572     PISSN: 0003410X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

References (13)

1. Hepatitis B virus infection markers in genetic hemochromatosis: A study of 272 patients
2. Yersinia enterotocolitica
3. Low-molecular-weight iron complexes and oxygen radical reactions in idiopathic haemochromatosis
4. A novel MHC class1-like gene is mutated in patients with hereditary hemochromatosis
5. EASL International Consensus Conference on Haemochromatosis
6. Molecular medicine and hemochromatosis: At the crossroads
7. HFE mutations analysis in 711 hemochromatosis probands: Evidence for S65C implication in mild form of hemochromatosis
8. Haemochromatosis: Novel gene discovery and the molecular pathophysiology of iron metabolism
9. Hemochromatosis and the interaction of classical medicine and molecular biology
10. Inhibition of hepatitis B virus production associated with high levels of intracellular viral DNA intermediates in iron-depleted HepG2.2.15 cells
11. Iron reduction before and during interferon therapy of chronic hepatitis C: Results of a multicenter, randomized, controlled trial