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4. Screening for iron overload and HFE mutations in a university hospital. Remacha AF; Carrasco M; Sardà MP; Barceló MJ; Blesa I; Baiget M Haematologica; 2000 Aug; 85(8):873-4. PubMed ID: 10942939 [No Abstract] [Full Text] [Related]
5. [Prevalence of hereditary hemochromatosis among healthy workers. Diagnostic value of transferrin saturation assay]. Martínez-Vázquez C; Martínez Cadilla J; Gil M; Sopeña B; Torres J; Cordeiro E; Seijas M; de la Fuente J; Méndez MJ An Med Interna; 2000 Dec; 17(12):628-31. PubMed ID: 11213576 [TBL] [Abstract][Full Text] [Related]
6. Diagnostic efficacy of screening tests for hereditary hemochromatosis. Borwein S; Ghent CN; Valberg LS Can Med Assoc J; 1984 Oct; 131(8):895-901. PubMed ID: 6593112 [TBL] [Abstract][Full Text] [Related]
8. Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience. De Gobbi M; D'Antico S; Castagno F; Testa D; Merlini R; Bondi A; Camaschella C Haematologica; 2004 Oct; 89(10):1161-7. PubMed ID: 15477198 [TBL] [Abstract][Full Text] [Related]
9. [Modern diagnosis and treatment methods in hereditary hemochromatosis]. Loginov AS; Tokarev IuN; Settarova DA; Sukhareva GV Ter Arkh; 1988; 60(10):117-21. PubMed ID: 3222734 [TBL] [Abstract][Full Text] [Related]
10. Prevalence of idiopathic hemochromatosis in Italy: study of 1301 blood donors. Velati C; Piperno A; Fargion S; Colombo S; Fiorelli G Haematologica; 1990; 75(4):309-12. PubMed ID: 2276675 [TBL] [Abstract][Full Text] [Related]
11. Population screening for hemochromatosis: a comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors. Adams PC; Kertesz AE; McLaren CE; Barr R; Bamford A; Chakrabarti S Hepatology; 2000 May; 31(5):1160-4. PubMed ID: 10796893 [TBL] [Abstract][Full Text] [Related]
12. [Biologic update on hemochromatosis]. Bourel M; Brissot P; Simon M Bull Acad Natl Med; 1985 Mar; 169(3):423-31. PubMed ID: 3899315 [No Abstract] [Full Text] [Related]
13. Primary hemochromatosis in childhood. Escobar GJ; Heyman MB; Smith WB; Thaler MM Pediatrics; 1987 Oct; 80(4):549-54. PubMed ID: 3658574 [TBL] [Abstract][Full Text] [Related]
14. [Diagnosis of primary hemochromatosis]. Niederau C; Stremmel W; Strohmeyer G Dtsch Med Wochenschr; 1988 Oct; 113(42):1644-7. PubMed ID: 3181016 [No Abstract] [Full Text] [Related]
15. Maintaining iron balance in women blood donors of childbearing age: summary of a workshop. Bianco C; Brittenham G; Gilcher RO; Gordeuk VR; Kushner JP; Sayers M; Chambers L; Counts RB; Aylesworth C; Nemo G; Alving B Transfusion; 2002 Jun; 42(6):798-805. PubMed ID: 12147035 [No Abstract] [Full Text] [Related]
16. Genetic linkage between hereditary hemochromatosis and HLA. Kravitz K; Skolnick M; Cannings C; Carmelli D; Baty B; Amos B; Johnson A; Mendell N; Edwards C; Cartwright G Am J Hum Genet; 1979 Sep; 31(5):601-19. PubMed ID: 507053 [TBL] [Abstract][Full Text] [Related]
17. HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overload. Remacha AF; Carrasco M; Sardá MP; Barceló MJ; Baiget M Haematologica; 1999 Mar; 84(3):284-5. PubMed ID: 10189401 [No Abstract] [Full Text] [Related]
18. The effect of transferrin polymorphisms on iron metabolism. Lee PL; Ho NJ; Olson R; Beutler E Blood Cells Mol Dis; 1999; 25(5-6):374-9. PubMed ID: 10660486 [TBL] [Abstract][Full Text] [Related]
19. A population-based study of the clinical expression of the hemochromatosis gene. Olynyk JK; Cullen DJ; Aquilia S; Rossi E; Summerville L; Powell LW N Engl J Med; 1999 Sep; 341(10):718-24. PubMed ID: 10471457 [TBL] [Abstract][Full Text] [Related]
20. An HLA study in 74 Danish haemochromatosis patients and in 21 of their families. Milman N; Graudal N; Nielsen LS; Fenger K Clin Genet; 1992 Jan; 41(1):6-11. PubMed ID: 1633650 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]