Molekulargenetische Analyse und klinische Aspekte bei Patienten mit hereditärer Hämochromatose
Author:
Publisher
Springer Science and Business Media LLC
Subject
Orthopedics and Sports Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00132-014-2318-y.pdf
Reference30 articles.
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2. Axford JS, Bomford A, Revell P et al (1991) Hip arthropathy in genetic hemochromatosis. Radiographic and histologic features. Arthritis Rheum 34:357–361
3. Bulaj ZJ, Ajioka RS, Philips JD et al (2000) Disease-related conditions in relatives of patients with hemochromatosis. N Engl J Med 343:1529–1535
4. Cairo G, Recalcati S, Montosi G et al (1997) Inappropriately high iron regulatory protein activity in monocytes of patients with genetic hemochromatosis. Blood 89:2546–2553
5. Conte D, Manachino D, Colli A et al (1998) Prevalence of genetic hemochromatosis in a cohort of Italian patients with diabetes mellitus. Ann Intern Med 128:370–373
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1. Joint manifestations revealing inborn metabolic diseases in adults: a narrative review;Orphanet Journal of Rare Diseases;2023-08-10
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