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Juvenile hemochromatosis

Known as: Hemochromatosis, type 2, HEMOCHROMATOSIS, JUVENILE, hemochromatosis juvenile 
 
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Expression of hepcidin, a key regulator of intestinal iron absorption, can be induced in vitro by several bone morphogenetic… Expand
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Highly Cited
2009
Highly Cited
2009
Juvenile hemochromatosis is an iron-overload disorder caused by mutations in the genes encoding the major iron regulatory hormone… Expand
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Highly Cited
2007
Highly Cited
2007
Hemojuvelin (HJV) positively modulates the iron regulator hepcidin, and its mutations are the major cause of juvenile… Expand
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Highly Cited
2006
Highly Cited
2006
Hepcidin is a key regulator of systemic iron homeostasis. Hepcidin deficiency induces iron overload, whereas hepcidin excess… Expand
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Highly Cited
2005
Highly Cited
2005
Hereditary hemochromatosis is an iron-overload disorder resulting from mutations in proteins presumed to be involved in the… Expand
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Highly Cited
2005
Highly Cited
2005
Iron homeostasis plays a critical role in many physiological processes, notably synthesis of heme proteins. Dietary iron sensing… Expand
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Highly Cited
2004
Highly Cited
2004
Juvenile hemochromatosis is an early-onset autosomal recessive disorder of iron overload resulting in cardiomyopathy, diabetes… Expand
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Highly Cited
2003
Highly Cited
2003
Animal models indicate that the antimicrobial peptide hepcidin (HAMP; OMIM 606464) is probably a key regulator of iron absorption… Expand
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Review
2002
Review
2002
Juvenile hemochromatosis or type 2 hemochromatosis is a rare inherited recessive disease, which leads to severe iron overload… Expand
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Highly Cited
1999
Highly Cited
1999
Juvenile hemochromatosis (JH) is an autosomal recessive disorder that leads to severe iron loading in the 2d to 3d decade of life… Expand
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