Is activity restriction appropriate for patients with hereditary spherocytosis? A population-based analysis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-012-1665-1.pdf
Reference9 articles.
1. Perrotta S, Gallagher PG, Mohandas N (2008) Hereditary spherocytosis. Lancet 372:1411–1426
2. Bolton-Maggs PHB, Langer JC, Iolascon A et al (2012) Guidelines for the diagnosis and management of hereditary spherocytosis—2011 update. Br J Haematol 156:37–49
3. Eber S, Lux SE (2004) Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer. Semin Hematol 41:118–141
4. An X, Mohandas N (2008) Disorders of red cell membrane. Br J Haematol 141:367–375
5. Mullier F, Lainey E, Fenneteau O et al (2010) Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study. Ann Hematol 90:759–768
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