Literature DB >> 2657265

Hemochromatosis.

H K Holland1, J L Spivak.   

Abstract

This article discusses the pathophysiology and clinical manifestations of idiopathic and secondary hemochromatosis. Pedigree studies documenting the hereditary evidence for hemochromatosis are discussed. Current theories for the molecular mechanisms that result in iron overload are presented. Diagnostic strategies for assessing hemochromatosis and therapeutic modalities are reviewed.

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Year:  1989        PMID: 2657265     DOI: 10.1016/s0025-7125(16)30641-1

Source DB:  PubMed          Journal:  Med Clin North Am        ISSN: 0025-7125            Impact factor:   5.456


  1 in total

1.  Multiple organ dysfunction in a 33-year-old woman due to hereditary hemochromatosis.

Authors:  Y Niihara; D W Brouwer; K A Cantos
Journal:  West J Med       Date:  1995-04
  1 in total

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