(Q43836105)

27 November 2017

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1554800

8 October 2022

author name string

S. W. Eber

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1554800

8 October 2022

A. Pekrun

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1554800

8 October 2022

A. Neufeldt

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1554800

8 October 2022

W. Schröter

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1554800

8 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1554800

8 October 2022

publication date

1 February 1992

1 reference

27 November 2017

1 reference

27 November 2017

64

1 reference

27 November 2017

88-92

1 reference

27 November 2017

2

1 reference

Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis

27 November 2017

1 reference

12 December 2020

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

1 reference

12 December 2020

Genetics of spherocytosis

1 reference

12 December 2020

[Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]

1 reference

12 December 2020

Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis

1 reference

12 December 2020

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

1 reference

12 December 2020

THE OSMOTIC RESISTANCE (FRAGILITY) OF HUMAN RED CELLS

1 reference

12 December 2020

High prevalence of increased osmotic fragility of red blood cells among Norwegian blood donors

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

1 reference

12 December 2020

Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis

1 reference

12 December 2020

A new test for the laboratory diagnosis of spherocytosis

1 reference

12 December 2020

Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane

1 reference

12 December 2020

Acidified glycerol lysis test: a screening test for spherocytosis

1 reference

12 December 2020

Diagnosis of hereditary spherocytosis in newborn infants

1 reference

12 December 2020

An improved acidified glycerol lysis test (AGLT) used to detect spherocytes in pregnancy

1 reference

12 December 2020

An evaluation of the acidified glycerol lysis test

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01715351

1 reference

27 November 2017

1 reference