Detection of paroxysmal nocturnal hemoglobinuria clones to exclude inherited bone marrow failure syndromes-Reference-Cited by-同舟云学术

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Detection of paroxysmal nocturnal hemoglobinuria clones to exclude inherited bone marrow failure syndromes

Published:2014-03-18 Issue:6 Volume:92 Page:467-470
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

DeZern Amy E.¹²,Symons Heather J.¹,Resar Linda S.²,Borowitz Michael J.³,Armanios Mary Y.¹,Brodsky Robert A.¹²

Affiliation:

1. The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins; The Johns Hopkins University School of Medicine; Baltimore MD USA

2. Division of Hematology; Department of Medicine; The Johns Hopkins University School of Medicine; Baltimore MD USA

3. Division of Hematopathology; Department of Pathology; The Johns Hopkins University School of Medicine; Baltimore MD USA

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12299/fullpdf

Reference14 articles.

1. Diagnosis, genetics, and management of inherited bone marrow failure syndromes;Alter;Hematology Am Soc Hematol Educ Program,2007

2. Pathophysiology and management of inherited bone marrow failure syndromes;Shimamura;Blood Rev,2010

3. Clinical management of aplastic anemia;Dezern;Expert Rev Hematol,2011

4. Clinical significance of a small population of paroxysmal nocturnal hemoglobinuria-type cells in the management of bone marrow failure;Nakao;Int J Hematol,2006

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