Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study

Author:

Mullier François,Lainey Elodie,Fenneteau Odile,Da Costa Lydie,Schillinger Françoise,Bailly Nicolas,Cornet Yvan,Chatelain Christian,Dogne Jean-Michel,Chatelain Bernard

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference21 articles.

1. King MJ, Behrens J, Rogers C, Flynn C, Greenwood D, Chambers K (2000) Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia. Br J Haematol 111(3):924–933

2. Bolton-Maggs PH, Stevens RF, Dodd NJ, Lamont G, Tittensor P, King MJ (2004) Guidelines for the diagnosis and management of hereditary spherocytosis. Br J Haematol 126(4):455–474

3. Perrotta S, Gallagher PG, Mohandas N (2008) Hereditary spherocytosis. Lancet 372(9647):1411–1426

4. Miraglia del Giudice E, Francese M, Polito R, Nobili B, Iolascon A, Perrotta S (1997) Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ank1) allele. Haematologica 82(3):332–333

5. An X, Mohandas N (2008) Disorders of red cell membrane. Br J Haematol 141(3):367–375

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