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International Journal of Neonatal Screening|May 27, 2026
Parents' Experiences of Receiving a Severe Combined Immunodeficiency (SCID) or Non-SCID T-Cell Lymphopenia Outcome During the Newborn Screening Evaluation in EnglandPru Holder, Chloe Musa, Jim B Chilcott, et al.BMC Cancer|May 22, 2020
The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani womenVictoria G Woof, Helen Ruane, David P French, et al.Journal of Medical Screening|December 4, 2019
Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani womenVictoria G Woof, Helen Ruane, Fiona Ulph, et al.Journal of Genetic Counseling|February 23, 2022
Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi ArabiaKhadijah H Bakur, Jumana Y Al-Aama, Zuhair N Alhassnan, et al.BMJ Open|October 2, 2020
Qualitative exploration of health professionals' experiences of communicating positive newborn bloodspot screening results for nine conditions in EnglandJane Chudleigh, Holly Chinnery, Jim R Bonham, et al.BMJ Open|December 14, 2020
Processing of positive newborn screening results: a qualitative exploration of current practice in EnglandJane Chudleigh, Holly Chinnery, Pru Holder, et al.BMJ Open|August 28, 2021
Process evaluation of co-designed interventions to improve communication of positive newborn bloodspot screening resultsJane Chudleigh, Pru Holder, Louise Moody, et al.Journal of Health Services Research & Policy|April 11, 2023
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 studyHooran M Khattak, Victoria G Woof, David P French, et al.Journal of Genetic Counseling|October 11, 2016
Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion GroupsIvan Eisler, Frances Flinter, Jo Grey, et al.European Journal of Human Genetics : EJHG|October 8, 2015
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery, Ivan Eisler, Matthew Ellison, et al.Pageof 6