Paroxysmal nocturnal hemoglobinuria clones in severe aplastic anemia patients treated with horse anti-thymocyte globulin plus cyclosporine

BACKGROUND: Clones of glycosylphosphatidylinositol-anchor protein-deficient cells are characteristic in paroxysmal nocturnal hemoglobinuria and are present in about 40–50% of patients with severe aplastic anemia. Flow cytometry has allowed for sensitive and precise measurement of glycosylphosphatidy...

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Autores principales: Scheinberg, Phillip, Marte, Michael, Nunez, Olga, Young, Neal S.
Formato: Artigo
Lenguaje:Inglês
Publicado: Ferrata Storti Foundation 2010
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Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2895030/
https://ncbi.nlm.nih.gov/pubmed/20595102
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2009.017889
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