User menu

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

Bibliographic reference Mullier, François ; Lainey, Elodie ; Fenneteau, Odile ; Da Costa, Lydie ; Schillinger, Françoise ; et. al. Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.. In: Annals of Hematology, Vol. 90, no.7, p. 759-68 (2011)
Permanent URL
  1. King May-Jean, Behrens Judith, Rogers Chris, Flynn Clare, Greenwood David, Chambers Keith, Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia, 10.1046/j.1365-2141.2000.02416.x
  2. Bolton-Maggs P. H. B., Stevens R. F., Dodd N. J., Lamont G., Tittensor P., King M.-J., , Guidelines for the diagnosis and management of hereditary spherocytosis, 10.1111/j.1365-2141.2004.05052.x
  3. Perrotta Silverio, Gallagher Patrick G, Mohandas Narla, Hereditary spherocytosis, 10.1016/s0140-6736(08)61588-3
  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
  6. Cynober Therese, Mohandas Narla, Tchernia Gil, Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity, 10.1016/s0022-2143(96)90027-x
  7. Michaels Lisa A., Cohen Alan R., Zhao Huaqing, Raphael Robert I., Manno Catherine S., Screening for hereditary spherocytosis by use of automated erythrocyte indexes, 10.1016/s0022-3476(97)70283-x
  8. Kutter D, Coulon N, Stirn F, Thoma M, Janecki J (2002) Demonstration and quantification of “hyperchromic” erythrocytes by haematological analysers. Application to screening for hereditary and acquired spherocytosis. Clin Lab 48(3–4):163–170
  9. Da Costa L., Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia, 10.1182/blood.v98.10.2894
  10. Chiron M., Cynober T., Mielot F., Tchernia G., Croisille L., The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis, 10.1007/s00282-999-0113-8
  11. Girodon François, Garçon Loïc, Bergoin Emilie, Largier Marie, Delaunay Jean, Fénéant-Thibault Madeleine, Maynadié Marc, Couillaud Gérard, Moreira Sophie, Cynober Thérèse, Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis, 10.1111/j.1365-2141.2007.06944.x
  12. King May-Jean, Telfer Paul, MacKinnon Heather, Langabeer Lisa, McMahon Corrina, Darbyshire Philip, Dhermy Didier, Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis, 10.1002/cyto.b.20413
  13. Urrechaga Eloísa, Borque Luís, Escanero Jesús F., Potential utility of the new Sysmex XE 5000 red blood cell extended parameters in the study of disorders of iron metabolism, 10.1515/cclm.2009.301
  14. Saada Véronique, Cynober Thérèse, Brossard Yves, Schischmanoff Pierre Olivier, Sender Alfred, Cohen Henri, Delaunay Jean, Tchernia Gil, INCIDENCE OF HEREDITARY SPHEROCYTOSIS IN A POPULATION OF JAUNDICED NEONATES, 10.1080/08880010600646662
  15. Sgro M., Incidence and causes of severe neonatal hyperbilirubinemia in Canada, 10.1503/cmaj.060328
  16. Blanc L., Liu J., Vidal M., Chasis J. A., An X., Mohandas N., The water channel aquaporin-1 partitions into exosomes during reticulocyte maturation: implication for the regulation of cell volume, 10.1182/blood-2009-06-230086
  17. HARRIS NEIL, JOU JOSEP MARIA, DEVOTO GIANLUIGI, LOTZ J., PAPPAS JAMES, WRANOVICS DAVID, WILKINSON MARY, FLETCHER SUZANNE R., KRATZ ALEXANDER, Performance Evaluation of the ADVIA 2120 Hematology Analyzer: An International Multicenter Clinical Trial, 10.1532/lh96.04064
  18. Banfi Giuseppe, Mauri Clara, Morelli Benedetto, Gaetano Nicola Di, Malgeri Ursula, Melegati Gianluca, Reticulocyte count, mean reticulocyte volume, immature reticulocyte fraction, and mean sphered cell volume in elite athletes: reference values and comparison with the general population, 10.1515/cclm.2006.094
  19. Rodrigues Ana, Ortega Carlos, Santos Luís, Teixeira Alexandre, Dinis Maria Joáo, Vasconcelos Iponina, Lacerda Jorge, Fonseca Elisa, Clinical Utility Of Beckman-Coulter Gen's Reticulocyte Analysis in the Study of Anemia of Chronic Disease (ACD), 10.1532/lh96.07007
  20. URRECHAGA E., Clinical utility of the new beckman-coulter parameter red blood cell size factor in the study of erithropoiesis, 10.1111/j.1751-553x.2008.01088.x
  21. Bruce Lesley J, C Robinson Hannah, Guizouarn Hélène, Borgese Franck, Harrison Penny, King May-Jean, Goede Jeroen S, Coles Suzanne E, Gore Daniel M, Lutz Hans U, Ficarella Romina, Layton D Mark, Iolascon Achille, Ellory J Clive, Stewart Gordon W, Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1, 10.1038/ng1656