Testing for hereditary spherocytosis: a French experience. (Q36661988)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23204481%20AND%20SRC:MED&resulttype=core&format=json

19 February 2020

title

Testing for hereditary spherocytosis: a French experience (English)

1 reference

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19 February 2020

main subject

hereditary spherocytosis

1 reference

3

1 reference

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19 February 2020

author name string

Caroline Mayeur-Rousse

1

1 reference

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19 February 2020

Mélanie Gentil

2

1 reference

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19 February 2020

Madeleine Fénéant Thibaut

4

1 reference

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19 February 2020

Corinne Guitton

5

1 reference

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19 February 2020

Véronique Picard

6

1 reference

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19 February 2020

publication date

1 December 2012

1 reference

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19 February 2020

1 reference

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19 February 2020

volume

97

1 reference

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19 February 2020

issue

12

1 reference

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19 February 2020

page(s)

e48-9; author reply e52

1 reference

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Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics

19 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3590076

30 September 2017

Hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3590076

Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3590076

Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3590076

Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3590076

Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia

20 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23204481

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocyto

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23204481

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3324/HAEMATOL.2012.074070

1 reference

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19 February 2020

1 reference

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19 February 2020

PubMed publication ID

23204481

1 reference