Detection of paroxysmal nocturnal hemoglobinuria clones to exclude inherited bone marrow failure syndromes (Q34164117)

31 July 2017

title

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

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paroxysmal nocturnal hemoglobinuria

31 July 2017

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Amy E DeZern

1

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31 July 2017

Heather J Symons

2

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31 July 2017

Linda S Resar

3

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31 July 2017

Michael J Borowitz

4

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31 July 2017

Mary Y Armanios

5

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31 July 2017

Robert A Brodsky

6

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31 July 2017

publication date

18 March 2014

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European Journal of Haematology

31 July 2017

published in

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31 July 2017

volume

92

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31 July 2017

issue

6

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31 July 2017

page(s)

467-470

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31 July 2017

cites work

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5 July 2018

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5 July 2018

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5 July 2018

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Clinical significance of a small population of paroxysmal nocturnal hemoglobinuria-type cells in the management of bone marrow failure

5 July 2018

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5 July 2018

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5 July 2018

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Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

5 July 2018

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Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise?

5 July 2018

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5 July 2018

1 reference

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Bone marrow failure in Shwachman-Diamond syndrome does not select for clonal haematopoiesis of the paroxysmal nocturnal haemoglobinuria phenotype

28 October 2018

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Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia

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Criteria for severe aplastic anaemia

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inferred from PubMed ID database lookup

12 December 2020

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Identifiers

DOI

10.1111/EJH.12299

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31 July 2017

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31 July 2017

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