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HFE genotype modifies the influence of heme iron intake on iron status.
Greenwood DC, Cade JE, Moreton JA, O'Hara B, Burley VJ, Randerson-Moor JA, Kukalizch K, Thompson D, Worwood M, Bishop DT. Greenwood DC, et al. Among authors: worwood m. Epidemiology. 2005 Nov;16(6):802-5. doi: 10.1097/01.ede.0000181306.85583.ea. Epidemiology. 2005. PMID: 16222171 Free article.
HFE mutations, iron deficiency and overload in 10,500 blood donors.
Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M. Jackson HA, et al. Among authors: worwood m. Br J Haematol. 2001 Aug;114(2):474-84. doi: 10.1046/j.1365-2141.2001.02949.x. Br J Haematol. 2001. PMID: 11529872 Free article.
HFE Mutations as risk factors in disease.
Worwood M. Worwood M. Best Pract Res Clin Haematol. 2002 Jun;15(2):295-314. Best Pract Res Clin Haematol. 2002. PMID: 12401309 Review.
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
Livesey KJ, Wimhurst VL, Carter K, Worwood M, Cadet E, Rochette J, Roberts AG, Pointon JJ, Merryweather-Clarke AT, Bassett ML, Jouanolle AM, Mosser A, David V, Poulton J, Robson KJ. Livesey KJ, et al. Among authors: worwood m. J Med Genet. 2004 Jan;41(1):6-10. doi: 10.1136/jmg.2003.008805. J Med Genet. 2004. PMID: 14729817 Free PMC article.
190 results