Results 161 to 170 of about 28,106 (200)
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Neonatal hemochromatosis

Gastroenterology Clinics of North America, 2003
Neonatal hemochromatosis is a rare gestational condition in which iron accumulates in the fetal tissues in a distribution like that seen in hereditary hemochromatosis. Extensive liver damage is the dominant clinical feature, with late fetal loss or early neonatal death. NH recurs within sibships at a rate higher than that predicted for simple Mendelian
Knisely, A S   +2 more
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Hemochromatosis and Vitiligo

Archives of Dermatology, 1964
The case history of a 47-year-old male patient with vitiligo and hemochromatosis is reported. Skin biopsies disclose the uniform distribution of iron pigmentation, although the vitiligo spots seem to be deficient in melanin as opposed to the dark-colored skin areas where contents of melanin apparently have increased.
A, PERDRUP, H, POULSEN
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HEMOCHROMATOSIS AND THE HEART

Annals of Internal Medicine, 1957
Excerpt In Sheldon's1classic monograph on hemochromatosis, myocardial failure is mentioned as an uncommon cause of death.
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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

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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HEREDITARY HEMOCHROMATOSIS

Nursing Clinics of North America, 2000
Hereditary hemochromatosis (HH) is an autosomal recessive iron overload disorder that affects more than one million Americans. This underdiagnosed disorder is associated with high morbidity and mortality, which can be prevented with early identification and treatment.
openaire   +2 more sources

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