Medical progress - Hereditary hemochromatosis - A new look at an old disease

[1] Clinical consequences of iron overload in hemochromatosis homozygotes [J]. BLOOD, 2003, 101 (09) : 3351 - 3354

[2] Andrews NC, 1999, NUTR REV, V57, P114, DOI 10.1111/j.1753-4887.1999.tb06934.x

[3] A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient [J]. GUT, 2003, 52 (08) : 1215 - 1217

[4] Åsberg A, 2001, SCAND J GASTROENTERO, V36, P1108

[5] IRON CONTENT OF JEJUNAL MUCOSA OBTAINED BY CROSBYS BIOPSY IN HEMOCHROMATOSIS AND HEMOSIDEROSIS [J]. BLOOD-THE JOURNAL OF HEMATOLOGY, 1966, 28 (01): : 70 - &

[6] The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis [J]. BLOOD, 2003, 101 (09) : 3347 - 3350

[7] Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA [J]. LANCET, 2002, 359 (9302) : 211 - 218

[8] BOTHWELL TH, 1995, NUTR REV, V53, P237, DOI 10.1111/j.1753-4887.1995.tb05480.x

[9] Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis [J]. LANCET, 2003, 361 (9358) : 669 - 673

[10] Hemochromatosis-associated morbidity in the United States: An analysis of the National Hospital Discharge Survey, 1979-1997 [J]. GENETICS IN MEDICINE, 2001, 3 (02) : 109 - 111

[1] Clinical consequences of iron overload in hemochromatosis homozygotes [J]. BLOOD, 2003, 101 (09) : 3351 - 3354

[2] Andrews NC, 1999, NUTR REV, V57, P114, DOI 10.1111/j.1753-4887.1999.tb06934.x

[3] A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient [J]. GUT, 2003, 52 (08) : 1215 - 1217

[4] Åsberg A, 2001, SCAND J GASTROENTERO, V36, P1108

[5] IRON CONTENT OF JEJUNAL MUCOSA OBTAINED BY CROSBYS BIOPSY IN HEMOCHROMATOSIS AND HEMOSIDEROSIS [J]. BLOOD-THE JOURNAL OF HEMATOLOGY, 1966, 28 (01): : 70 - &

[6] The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis [J]. BLOOD, 2003, 101 (09) : 3347 - 3350

[7] Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA [J]. LANCET, 2002, 359 (9302) : 211 - 218

[8] BOTHWELL TH, 1995, NUTR REV, V53, P237, DOI 10.1111/j.1753-4887.1995.tb05480.x

[9] Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis [J]. LANCET, 2003, 361 (9358) : 669 - 673

[10] Hemochromatosis-associated morbidity in the United States: An analysis of the National Hospital Discharge Survey, 1979-1997 [J]. GENETICS IN MEDICINE, 2001, 3 (02) : 109 - 111