Diagnosis and therapy of genetic haemochromatosis (review and 2017 update)-Reference-Cited by-同舟云学术

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Diagnosis and therapy of genetic haemochromatosis (review and 2017 update)

Published:2018-04-16 Issue:3 Volume:181 Page:293-303
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Fitzsimons Edward J.¹,Cullis Jonathan O.²^ORCID,Thomas Derrick W.³^ORCID,Tsochatzis Emmanouil⁴,Griffiths William J. H.⁵^ORCID,

Affiliation:

1. Department of Haematology; Gartnavel General Hospital; Glasgow UK

2. Department of Haematology; Salisbury NHS Foundation Trust; Salisbury UK

3. Department of Haematology; Plymouth Hospitals NHS Trust; Plymouth UK

4. UCL Institute for Liver and Digestive Health; Royal Free London NHS Foundation Trust and UCL; London UK

5. Department of Hepatology; Cambridge University Hospitals NHS Foundation Trust; Cambridge UK

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.15164/fullpdf

Reference45 articles.

1. Haemochromatosis;Adams;Lancet,2007

2. Longterm survival analysis in hereditary haemochromatosis;Adams;Gastroenterology,1991

3. Comparison of the unsaturated iron binding capacity with transferrin saturation as a screening test to detect C282Y homozygotes for haemochromatosis in 101,168 participants in the HEIRS study;Adams;Clinical Chemistry,2005a

4. Hemochromatosis and iron-overload screening in a racially diverse population;Adams;The New England Journal of Medicine,2005b

5. Iron-overload-related disease in HFE hereditary hemochromatosis;Allen;The New England Journal of Medicine,2008

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