Musculoskeletal disease burden of hereditary hemochromatosis

Author:

Sahinbegovic Enijad,Dallos Tomáš,Aigner Elmar,Axmann Roland,Manger Bernhard,Englbrecht Matthias,Schöniger-Hekele Maximilian,Karonitsch Thomas,Stamm Tanja,Farkas Martin,Karger Thomas,Stölzel Ulrich,Keysser Gernot,Datz Christian,Schett Georg,Zwerina Jochen

Funder

DFG Focus Programme SPP 1468 “Osteoimmunology-IMMUNOBONE: A program to unravel the mutual interactions between the immune system and bone”

German Ministry for Education and Research ANCYLOSS project

Spondyloarthritis Immunology Research Alliance

European Union projects Masterswitch, Kinacept, and Adipoa

German Society of Rheumatology

Interdisciplinary Centre for Clinical Research at the University of Erlangen-Nuremberg

Articulum Fellowship

Publisher

Wiley

Subject

Pharmacology (medical),Immunology,Rheumatology,Immunology and Allergy

Reference26 articles.

1. Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis;Niederau;N Engl J Med,1985

2. The endocrine manifestations of hemochromatosis;McNeil;Am J Med Sci,1983

3. Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis;Datz;J Hepatol,1997

4. Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany;Meier;Clin Lab,2005

5. The penetrance of hereditary hemochromatosis;Waalen;Best Pract Res Clin Haematol,2005

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