(Q38088425)

28 August 2017

Hereditary red cell membrane disorders and laboratory diagnostic testing (English)

1 reference

28 August 2017

M-J King

1

1 reference

PubMed ID

23480868

28 August 2017

A Zanella

series ordinal

2

1 reference

28 August 2017

11 March 2013

1 reference

International Journal of Laboratory Hematology

28 August 2017

1 reference

28 August 2017

35

1 reference

28 August 2017

237-243

1 reference

28 August 2017

3

1 reference

Defining the architecture of the red blood cell membrane: newer biophysical approaches

28 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Cell surface organization by the membrane skeleton.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Red cell membrane: past, present, and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

New insights into regulation of erythrocyte shape

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Hemolytic disease due to membrane ion channel disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Hereditary elliptocytosis: spectrin and protein 4.1R.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Red cell membrane Na+ transport systems in hereditary spherocytosis: relevance to understanding the increased Na+ permeability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

21 January 2018

Hereditary spherocytosis

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

Hereditary stomatocytosis and cation-leaky red cells--recent developments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12070

21 January 2018

Identifiers

DOI

10.1111/IJLH.12070

1 reference

28 August 2017

1 reference

PubMed ID

23480868