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hemochromatosis
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References
These sources were used to develop the Genetics Home Reference
condition summary
on hemochromatosis.
Alexander J, Kowdley KV. Hereditary hemochromatosis: genetics, pathogenesis, and clinical management. Ann Hepatol. 2005 Oct-Dec;4(4):240-7. Review.
PubMed citation
Anderson GJ, Powell LW. HFE and non-HFE hemochromatosis. Int J Hematol. 2002 Oct;76(3):203-7. Review.
PubMed citation
Beutler E. Hemochromatosis: genetics and pathophysiology. Annu Rev Med. 2006;57:331-47. Review.
PubMed citation
Camaschella C, Roetto A, Cali A, De Gobbi M, Garozzo G, Carella M, Majorano N, Totaro A, Gasparini P. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. Nat Genet. 2000 May;25(1):14-5.
PubMed citation
Camaschella C, Roetto A, De Gobbi M. Juvenile hemochromatosis. Semin Hematol. 2002 Oct;39(4):242-8. Review.
PubMed citation
De Gobbi M, Roetto A, Piperno A, Mariani R, Alberti F, Papanikolaou G, Politou M, Lockitch G, Girelli D, Fargion S, Cox TM, Gasparini P, Cazzola M, Camaschella C. Natural history of juvenile haemochromatosis. Br J Haematol. 2002 Jun;117(4):973-9. Review.
PubMed citation
Dolbey CH. Hemochromatosis: a review. Clin J Oncol Nurs. 2001 Nov-Dec;5(6):257-60. Review.
PubMed citation
Heeney MM, Andrews NC. Iron homeostasis and inherited iron overload disorders: an overview. Hematol Oncol Clin North Am. 2004 Dec;18(6):1379-403.
PubMed citation
Kelly AL, Lunt PW, Rodrigues F, Berry PJ, Flynn DM, McKiernan PJ, Kelly DA, Mieli-Vergani G, Cox TM. Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism. J Med Genet. 2001 Sep;38(9):599-610.
PubMed citation
Knisely AS, Mieli-Vergani G, Whitington PF. Neonatal hemochromatosis. Gastroenterol Clin North Am. 2003 Sep;32(3):877-89, vi-vii. Review.
PubMed citation
Le Gac G, Ferec C. The molecular genetics of haemochromatosis. Eur J Hum Genet. 2005 Nov;13(11):1172-85. Review.
PubMed citation
Montosi G, Donovan A, Totaro A, Garuti C, Pignatti E, Cassanelli S, Trenor CC, Gasparini P, Andrews NC, Pietrangelo A. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. J Clin Invest. 2001 Aug;108(4):619-23.
PubMed citation
Njajou OT, Vaessen N, Joosse M, Berghuis B, van Dongen JW, Breuning MH, Snijders PJ, Rutten WP, Sandkuijl LA, Oostra BA, van Duijn CM, Heutink P. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis. Nat Genet. 2001 Jul;28(3):213-4.
PubMed citation
Pietrangelo A. Hereditary hemochromatosis--a new look at an old disease. N Engl J Med. 2004 Jun 3;350(23):2383-97. Review. No abstract available.
PubMed citation
Pietrangelo A. Non-HFE hemochromatosis. Hepatology. 2004 Jan;39(1):21-9. Review. No abstract available.
PubMed citation
Pietrangelo A. Non-HFE hemochromatosis. Semin Liver Dis. 2005 Nov;25(4):450-60. Review.
PubMed citation
Pietrangelo A. The ferroportin disease. Blood Cells Mol Dis. 2004 Jan-Feb;32(1):131-8. Review.
PubMed citation
Wheeler CJ, Kowdley KV. Hereditary hemochromatosis: a review of the genetics, mechanism, diagnosis, and treatment of iron overload. Compr Ther. 2006 Spring;32(1):10-6.
PubMed citation
Whitington PF. Fetal and infantile hemochromatosis. Hepatology. 2006 Apr;43(4):654-60. Review. No abstract available.
PubMed citation
Yen AW, Fancher TL, Bowlus CL. Revisiting hereditary hemochromatosis: current concepts and progress. Am J Med. 2006 May;119(5):391-9. Review.
PubMed citation
Reviewed: October 2006
Published: January 23, 2009