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1.
The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani women.
BMC Cancer
; 20(1): 452, 2020 May 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-32434564
2.
Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.
Mol Genet Metab
; 113(4): 301-6, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25458521
3.
The role of knowledge, primary care and community engagement to improve breast-screening access for Pakistani women in the United Kingdom: A secondary analysis of a qualitative study.
J Health Serv Res Policy
; 28(3): 149-156, 2023 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-37039238
4.
Iron overload in the Asian community.
Blood
; 114(1): 20-5, 2009 Jul 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-19342478
5.
Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women.
J Med Screen
; 27(3): 130-137, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31791172
6.
How should health policy and practice respond to the increased genetic risk associated with close relative marriage? results of a UK Delphi consensus building exercise.
BMJ Open
; 9(7): e028928, 2019 07 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31289086
7.
Inclusion of diverse populations in genomic research and health services: Genomix workshop report.
J Community Genet
; 8(4): 267-273, 2017 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-28755064
8.
Community engagement and education: addressing the needs of South Asian families with genetic disorders.
J Community Genet
; 7(4): 317-323, 2016 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-27614444
9.
Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England.
J Community Genet
; 7(3): 215-28, 2016 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-27311843
10.
Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders.
Eur J Paediatr Neurol
; 20(2): 286-295, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26748598
11.
Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families.
J Community Genet
; 1(2): 73-81, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-22460207
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