Haemochromatosis — a clinical update
Author:
Affiliation:
1. Liver UnitQueensland Institute of Medical Research (QIMR)Joint Liver Program, QIMR and University of QueenslandBrisbaneQLD
Publisher
AMPCo
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.1996.tb122053.x
Reference27 articles.
1. vonRecklinghausenFD.Uber Haemochromatose.Tageblatt der (62) Versammlung deutscher Naturforscher und Arzte in Heidelberg.1889:324–325.
2. PowellLW JazwinskaE.HallidayJW. Primary iron overload. In:BrockJH HallidayJW PippardMJ PowellLW editors.Ironmetabolism in healthand disease. London: WB Saunders.1994:227–270.
3. Survival and Causes of Death in Cirrhotic and in Noncirrhotic Patients with Primary Hemochromatosis
4. Primary haemochromatosis: inherited or acquired?;MacDonald RA;Prog Hematol,1965
5. Prevalence of haemochromatosis amongst asymptomatic Australians
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1. Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia;Annals of Pediatric Endocrinology & Metabolism;2017
2. Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis;Endocrinology and Metabolism;2014
3. Genotyping as a diagnostic aid in genetic haemochromatosis;Journal of Gastroenterology and Hepatology;2002-04-19
4. Klinische und genetische Aspekte der hereditären Hämochromatose;Der Pathologe;2001-05-03
5. Haemochromatosis: Automated Detection of the Two Point Mutations in the HFE Gene: Cys282Tyr and His63Asp;Clinical Chemistry and Laboratory Medicine;2000-01-04
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