Diagnosis and management of hereditary haemochromatosis.

D W Swinkels, C Th B M van Deursen, M A van Bokhoven

Journal: BMJ (Clinical research ed.) 2011;342():c7251

PMID: 21248018

Abstract

Address: Department of General Practice, Maastricht University, School for Public Health and Primary Care CAPHRI, 6200 MD Maastricht, Netherlands. [email protected]

DOI: 10.1136/bmj.c7251

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MeSH Terms: Biopsy, Cytapheresis, Diagnosis, Differential, Early Diagnosis, Genetic Techniques, Hemochromatosis, Humans, Iron Chelating Agents, Liver, Magnetic Resonance Imaging, Mutation, Phlebotomy, Prognosis, Transferrin