Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics

BACKGROUND: The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-based or glycerol-based red cell osmotic fragility tests; more recently, an assay directly targeting the hereditary spherocytosis molecular defect (eosin-5′-maleimide-binding test) has been proposed. None of the...

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Bibliografske podrobnosti
Main Authors: Bianchi, Paola, Fermo, Elisa, Vercellati, Cristina, Marcello, Anna P., Porretti, Laura, Cortelezzi, Agostino, Barcellini, Wilma, Zanella, Alberto
Format: Artigo
Jezik:Inglês
Izdano: Ferrata Storti Foundation 2012
Teme:
Original Articles and Brief Reports
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3347664/
https://ncbi.nlm.nih.gov/pubmed/22058213
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2011.052845
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