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HEMOCHROMATOSIS, TYPE 1

Known as: HEMOCHROMATOSIS, HFE, HFE1 
National Institutes of Health

Papers overview

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Highly Cited
2004
Highly Cited
2004
Summary.  We analysed liver histology findings in a large cohort of patients with chronic hepatitis C and in roughly half of them… 
Highly Cited
2003
Highly Cited
2003
HFE is a nonclassical class I molecule that associates with beta 2-microglobulin (beta 2m) and with the transferrin receptor. HFE… 
Review
2003
Review
2003
HFE was discovered as the hereditary hemochromatosis (HH) gene. It is located on chromosome 6 (6p21.3), 4Mb telomeric to the HLA… 
Review
2001
Review
2001
BACKGROUND Hereditary hemochromatosis is an inherited disorder of iron metabolism that is characterized by excessive iron… 
2001
2001
The possible role of iron in facilitating the development of liver cancer is still debated. The aims of this study were to define… 
Highly Cited
2000
Highly Cited
2000
Hereditary hemochromatosis (HH) is a very common autosomal recessive disorder of iron metabolism and frequently associated with… 
Highly Cited
1999
Highly Cited
1999
It has been proposed that iron overload may adversely affect liver disease outcome. The recent identification of 2 mutations in… 
Highly Cited
1999
Highly Cited
1999
Hemochromatosis (HH) is usually caused by the homozygous state for C282Y mutation in the HFE gene. A minority of iron loaded… 
1999
1999
272 nature genetics • volume 23 • november 1999 In the August issue of Nature Genetics, Jeffrey et al.1 described a primer…