(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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Clinical management of aplastic anemia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

Pathophysiology and management of inherited bone marrow failure syndromes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

Diagnosis, genetics, and management of inherited bone marrow failure syndromes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

New Insights into the Pathophysiology of Acquired Cytopenias

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4161035

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

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24612308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24612308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Criteria for severe aplastic anaemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24612308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/EJH.12299

1 reference

31 July 2017

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31 July 2017

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