(Q47997379)

7 February 2018

http://europepmc.org/abstract/MED/24947683

title

Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice (English)

1 reference

7 February 2018

http://europepmc.org/abstract/MED/24947683

main subject

familial pseudohyperkalemia

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Lesley J Bruce

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Joanna F Flatt

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

author name string

Waleed M Bawazir

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Jonathan P Wallis

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Rebecca A Cardigan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Helen V New

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Michael Wiltshire

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Lizanne Page

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Catherine E Chapman

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Gordon W Stewart

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

publication date

19 June 2014

1 reference

7 February 2018

http://europepmc.org/abstract/MED/24947683

published in

Transfusion

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

volume

54

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

page(s)

3043-3050

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24947683%20AND%20SRC:MED&resulttype=core&format=json

Red cell changes during storage

9 June 2020

cites work

1 reference

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

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

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

21 January 2018

1 reference

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

21 January 2018

1 reference

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

21 January 2018

1 reference

Hemolytic disease due to membrane ion channel disorders

21 January 2018

1 reference

Familial pseudohyperkalaemia. A new syndrome

21 January 2018

1 reference

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

21 January 2018

1 reference

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

21 January 2018

1 reference

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

21 January 2018

1 reference

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

21 January 2018

1 reference

A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.

21 January 2018

1 reference

Neonatal mortality following transfusion of red cells with high plasma potassium levels

21 January 2018

1 reference

An unusual case of hyperkalaemia-induced cardiac arrest in a paediatric patient during transfusion of a 'fresh' 6-day-old blood unit

21 January 2018

1 reference

Cardiac arrests associated with hyperkalemia during red blood cell transfusion: a case series

21 January 2018

1 reference

Transfusion-associated hyperkalemic cardiac arrest in pediatric patients receiving massive transfusion.

21 January 2018

1 reference

Hyperkalaemia during rapid blood transfusion and hypovolaemic cardiac arrest in children

21 January 2018

1 reference

Transfusion-associated hyperkalemia

21 January 2018

1 reference

RBC storage and avoiding hyperkalemia from transfusions to neonates & infants

21 January 2018

1 reference