Bases moleculares e importancia clínica de los excepcionales fenotipos de grupo sanguíneo P y PK
Elena, Daniel De La Vega ; Hellberg, Asa LU ; Pivetta, Mario ; Raillon, Miguel Ángel ; Chialina, Sergio ; Solis, E. and Olsson, Martin L LU
(2008)
In Revista Cubana de Hematologia, Inmunologia y Hemoterapia
24(3).
- Abstract
All the cells of the individuals with phenotypes "p" y "Pk" lack the glucidic antigens of "public" blood groups. These subjects form natural and regular antibodies against the missing structures (anti-P, anti-PP1 y anti-PP1Pk) that agglutínate or hemolyze the red-blood cells of every individual, excepting those with the same phenotype. Due to the exceptional character of these pictures (a few individuals per million) and their association with severe transfusional hemolytic reactions and repeated miscarriages, these subjects should be identified and characterized.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/dfee3bf2-666c-4f0f-8885-9e840765c84f
- author
- Elena, Daniel De La Vega
; Hellberg, Asa
LU
; Pivetta, Mario
; Raillon, Miguel Ángel
; Chialina, Sergio
; Solis, E.
and Olsson, Martin L
LU
- organization
- alternative title
- Molecular bases and clinical importance of the exceptional phenotypes of blood group P and PK
- publishing date
- 2008-09
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Alloimmunization, Blood group, Erythrocyte, Gestation, Glycosyltransferases, Transfusion
- in
- Revista Cubana de Hematologia, Inmunologia y Hemoterapia
- volume
- 24
- issue
- 3
- publisher
- Editorial Ciencias Medicas
- external identifiers
-
- scopus:67649948944
- ISSN
- 0864-0289
- language
- Spanish
- LU publication?
- yes
- additional info
- Copyright: Copyright 2009 Elsevier B.V., All rights reserved.
- id
- dfee3bf2-666c-4f0f-8885-9e840765c84f
- alternative location
- http://scielo.sld.cu/pdf/hih/v24n3/hih02308.pdf
- date added to LUP
- 2021-08-04 12:52:57
- date last changed
- 2022-02-01 22:53:58
@article{dfee3bf2-666c-4f0f-8885-9e840765c84f,
abstract = {{<p>All the cells of the individuals with phenotypes "p" y "Pk" lack the glucidic antigens of "public" blood groups. These subjects form natural and regular antibodies against the missing structures (anti-P, anti-PP1 y anti-PP1Pk) that agglutínate or hemolyze the red-blood cells of every individual, excepting those with the same phenotype. Due to the exceptional character of these pictures (a few individuals per million) and their association with severe transfusional hemolytic reactions and repeated miscarriages, these subjects should be identified and characterized.</p>}},
author = {{Elena, Daniel De La Vega and Hellberg, Asa and Pivetta, Mario and Raillon, Miguel Ángel and Chialina, Sergio and Solis, E. and Olsson, Martin L}},
issn = {{0864-0289}},
keywords = {{Alloimmunization; Blood group; Erythrocyte; Gestation; Glycosyltransferases; Transfusion}},
language = {{spa}},
number = {{3}},
publisher = {{Editorial Ciencias Medicas}},
series = {{Revista Cubana de Hematologia, Inmunologia y Hemoterapia}},
title = {{Bases moleculares e importancia clínica de los excepcionales fenotipos de grupo sanguíneo P y P<sup>K</sup>}},
url = {{http://scielo.sld.cu/pdf/hih/v24n3/hih02308.pdf}},
volume = {{24}},
year = {{2008}},
}