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Hereditary hemochromatosis

Seminars in Hematology, 2002
Hereditary hemochromatosis (hh, type 1 hemochromatosis) is an autosomal recessive trait characterized by hyperabsorption of dietary iron. The disease trait occurs in approximately five per thousand Caucasians of northern European descent. The causative gene, designated HFE, was isolated and characterized in 1996; most individuals with hh are homozygous
Richard S, Ajioka, James P, Kushner
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Hereditary Hemochromatosis

2007
Iron is a major component of the Earth’s crust, but its own chemistry greatly limits utilization and also sets the basis for its toxicity. Hereditary hemochromatosis (HH) is the most common cause of iron overload in humans. For much of the twentieth century, HH was regarded as a monogenic disorder characterized by excess tissue deposits of iron ...
CORRADINI, Elena   +2 more
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Hemochromatosis

Archives of Internal Medicine, 1986
Hemochromatosis is a hereditary disorder of the control of iron metabolism wherein the absorptive intestine accepts from the diet more iron than the body requires; because no excretory mechanism exists, the excess must be deposited in storage organs, ultimately to their detriment.
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Hemochromatosis

Journal of Diagnostic Medical Sonography, 2009
Hemochromatosis is an iron metabolism disorder in which the intestines absorb excessive amounts of iron, which is eventually deposited into soft tissues. Hereditary hemochromatosis is the most common single-gene disorder in the US white population. Typically, adults do not begin to exhibit manifestations of the disease until the age of 40, after years
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Hemochromatosis

Southern Medical Journal, 1962
L Y, PESKOE, A, SIEGEL
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Hemochromatosis

The Guthrie Journal, 1956
J M, STEELE, R F, DAHLEN
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Hemochromatosis

The American Journal of Medicine, 1951
A, MARBLE, C C, BAILEY
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Neonatal Hemochromatosis

Pediatrics, 2001
K F, Murray, K V, Kowdley
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