(Q34230419)

English

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

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

0 references

hereditary spherocytosis

1 reference

based on heuristic

inferred from title

author name string

Paola Bianchi

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Elisa Fermo

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Cristina Vercellati

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Anna P Marcello

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Laura Porretti

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Agostino Cortelezzi

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Wilma Barcellini

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Alberto Zanella

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

4 November 2011

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

number of pages

8

1 reference

based on heuristic

inferred from page(s)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

97

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

516-523

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

THE OSMOTIC RESISTANCE (FRAGILITY) OF HUMAN RED CELLS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Red cell membrane disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Guidelines for the diagnosis and management of hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Cryohemolysis test as a diagnostic tool for hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Red blood cell membrane disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Hereditary spherocytosis: from clinical to molecular defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Glycerol lysis time of incubated erythrocytes in the diagnosis of hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

Normal erythrocyte osmotic fragility in hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

New tests for laboratory diagnosis of spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

6 July 2018

[Flowcytometric diagnostics of hereditary spherocytosis].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

The mutant erythrocyte band 3 protein in Southeast Asian ovalocytosis does not bind eosin-5-maleimide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Evaluation of eosin-5-maleimide flow cytometric test in diagnosis of hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Genotype/phenotype correlation in hereditary spherocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Flow cytometry as a diagnostic tool for hereditary spherocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

In vitro quantification of anti-red blood cell antibody production in idiopathic autoimmune haemolytic anaemia: effect of mitogen and cytokine stimulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3347664

28 October 2018

[Diagnostic value of acidified glycerol lysis test (AGLT) in hereditary spherocytosis and selected hematologic diseases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does preincubation of the red blood cells contribute to the capability of the osmotic fragility test to detect very mild forms of hereditary spherocytosis?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of acidified glycerol lysis test, Pink test and osmotic fragility test in hereditary spherocytosis: Effect of incubation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reliability of EMA binding test in the diagnosis of hereditary spherocytosis in Italian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usefulness of cryohemolysis test in the diagnosis of hereditary spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new test for the laboratory diagnosis of spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Experience with the glycerol lysis test in acid medium in diagnosis of hereditary spherocytosis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acidified glycerol lysis test: a screening test for spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic utility of the pre-incubated acidified glycerol lysis test in haemolytic and non-haemolytic anaemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cryohemolysis for the detection of hereditary spherocytosis: correlation studies with osmotic fragility and autohemolysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An evaluation of the acidified glycerol lysis test

1 reference

https://pubmed.ncbi.nlm.nih.gov/22058213

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3324/HAEMATOL.2011.052845

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34230419&oldid=1766485892"