Paroxysmal Nocturnal Hemoglobinuria Clones in Children with Acquired Aplastic Anemia: A Multicentre Study-Reference-Cited by-同舟云学术

Paroxysmal Nocturnal Hemoglobinuria Clones in Children with Acquired Aplastic Anemia: A Multicentre Study

Published:2014-07-09 Issue:7 Volume:9 Page:e101948
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Timeus Fabio,Crescenzio Nicoletta,Longoni Daniela,Doria Alessandra,Foglia Luiselda,Pagliano Sara,Vallero Stefano,Decimi Valentina,Svahn Johanna,Palumbo Giuseppe,Ruggiero Antonio,Martire Baldassarre,Pillon Marta,Marra Nicoletta,Dufour Carlo,Ramenghi Ugo,Saracco Paola

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference20 articles.

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2. Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia;C Sugimori;Blood,2006

3. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin;RA Brodsky;American Journal of Clinical Pathology,2000

4. Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry;MJ Borowitz;Cytometry Part B: Clinical Cytometry,2010

5. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals;DJ Araten;Proceeding of the National Academy of Sciences of the United States of America,1999

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