Lista de obras - Myfanwy Morgan - Dominio Público Uruguay

"I know he controls cancer": the meanings of religion among Black Caribbean and White British patients with advanced cancer.

artículo científico publicado en 2008

'Having a different conversation around death': diverse hospital chaplains' views on end-of-life care

artículo científico publicado en 2013

'I'll be in a safe place': a qualitative study of the decisions taken by people with advanced cancer to seek emergency department care

artículo científico publicado en 2016

'It doesn't do the care for you': a qualitative study of health care professionals' perceptions of the benefits and harms of integrated care pathways for end of life care

artículo científico publicado en 2015

'Seizure First Aid Training' for people with epilepsy who attend emergency departments, and their family and friends: study protocol for intervention development and a pilot randomised controlled trial.

artículo científico publicado en 2015

'The greatest thing in the world is the family': the meaning of social support among black Caribbean and white British patients living with advanced cancer

artículo científico publicado en 2011

11.5 Ethnic minorities and indigenous peoples

A nurse-led self-management intervention for people who attend emergency departments with epilepsy: the patients' view

artículo científico publicado en 2012

AN INTERVENTION TRIAL FOR PEOPLE WITH EPILEPSY ATTENDING A&E

Adjustment modes in the trajectory of progressive multiple sclerosis: a qualitative study and conceptual model

artículo científico publicado en 2016

An investigation of the predictors of photoprotection and UVR dose to the face in patients with XP: a protocol using observational mixed methods.

artículo científico publicado en 2017

Approaches to Photoprotection and Normalization in Highly Adherent Families of Children With Xeroderma Pigmentosum in the United Kingdom

artículo científico publicado en 2019

Assessing Treatment Fidelity within an Epilepsy Randomized Controlled Trial: Seizure First Aid Training for People with Epilepsy Who Visit Emergency Departments

artículo científico publicado en 2019

Attitudes to deceased organ donation and registration as a donor among minority ethnic groups in North America and the U.K.: a synthesis of quantitative and qualitative research

artículo científico publicado en 2012

Attitudes to kidney donation among primary care patients in rural Crete, Greece

artículo científico publicado en 2009

Attitudes to kidney donation and registering as a donor among ethnic groups in the UK

artículo científico publicado en 2006

Barriers to uptake and adherence with malaria prophylaxis by the African community in London, England: focus group study

artículo científico publicado en 2005

Bereaved donor families' experiences of organ and tissue donation, and perceived influences on their decision making

artículo científico publicado en 2018

Changes in diet and coronary heart disease mortality among social classes in Great Britain

artículo científico publicado en 1989

Continuity of care and intermediate outcomes of type 2 diabetes mellitus

artículo científico publicado en 2007

Dermatology quality of life scales--a measure of the impact of skin diseases

artículo científico publicado en 1997

Developing a model of short-term integrated palliative and supportive care for frail older people in community settings: perspectives of older people, carers and other key stakeholders.

artículo científico publicado en 2016

Developing and assessing the acceptability of an epilepsy first aid training intervention for patients who visit UK emergency departments: A multi-method study of patients and professionals.

artículo científico publicado en 2017

Developing patient-centred, feasible alternative care for adult emergency department users with epilepsy: protocol for the mixed-methods observational 'Collaborate' project

scientific article published on 02 November 2019

Development and evaluation of the feasibility and effects on staff, patients, and families of a new tool, the Psychosocial Assessment and Communication Evaluation (PACE), to improve communication and palliative care in intensive care and during [...]

artículo científico publicado en 2013

Doctors' Interviewing Technique and Its Response to Different Booking Time

article

Effect of social deprivation on blood pressure monitoring and control in England: a survey of data from the quality and outcomes framework

artículo científico publicado en 2008

Ethnic differences in behavioural risk factors for stroke: implications for health promotion.

artículo científico publicado en 2001

Ethnicity and attitudes to deceased kidney donation: a survey in Barbados and comparison with Black Caribbean people in the United Kingdom

artículo científico publicado en 2010

Ethnicity and registration as a kidney donor: the significance of identity and belonging.

artículo científico publicado en 2007

Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews

artículo científico publicado en 2013

Evaluating meta-ethnography: a synthesis of qualitative research on lay experiences of diabetes and diabetes care

artículo científico publicado en 2003

Evaluating meta-ethnography: systematic analysis and synthesis of qualitative research

artículo científico

Evaluation of a personalised adherence intervention to improve photoprotection in adults with Xeroderma Pigmentosum (XP): protocol for the trial of XPAND

scientific article published on 17 July 2019

Experience of and access to maternity care in the UK by immigrant women: a narrative synthesis systematic review

artículo científico publicado en 2019

Experience of continuity of care of patients with multiple long-term conditions in England

artículo científico publicado en 2009

Experiences of food access in hospital. A new questionnaire measure

artículo científico publicado en 2009

Experiences of stigma over the lifetime of people with xeroderma pigmentosum: A qualitative interview study in the United Kingdom

artículo científico

Explanations given by people with epilepsy for using emergency medical services: a qualitative study.

artículo científico publicado en 2012

Food-related Quality of Life in Inflammatory Bowel Disease: Development and Validation of a Questionnaire.

artículo científico publicado en 2015

Forms, interactions, and responses to social support: A qualitative study of support and adherence to photoprotection amongst patients with Xeroderma Pigmentosum

scientific article published on 22 November 2019

GPs' employment of locum doctors and satisfaction with their service.

artículo científico publicado en 2000

Handwritten 'post-it' notes, questionnaire formats and response to a postal questionnaire survey

article

Hospital inpatients' experiences of access to food: a qualitative interview and observational study

artículo científico publicado en 2008

How can a nurse intervention help people with newly diagnosed epilepsy? A qualitative study (of patients' views)

scientific article published on 01 January 2002

How can a nurse intervention help people with newly diagnosed epilepsy? A qualitative study of patients' views

scientific article published on 01 March 2003

How do patients referred to neurologists for headache differ from those managed in primary care?

artículo científico publicado en 2007

Human resources policies and continuity of care

artículo científico publicado en 2003

Illness doesn't belong to us ⬇️

artículo científico publicado el 1 de septiembre de 1997

Immigrant women's experiences of maternity-care services in Canada: a protocol for systematic review using a narrative synthesis.

artículo científico publicado en 2012

Immigrant women's experiences of maternity-care services in Canada: a systematic review using a narrative synthesis.

artículo científico publicado en 2015

Immigrant women's experiences of postpartum depression in Canada: a protocol for systematic review using a narrative synthesis

scientific article published on 21 August 2013

Implementing 'translational' biomedical research: convergence and divergence among clinical and basic scientists

artículo científico

Implementing the 2-week wait rule for cancer referral in the UK: general practitioners' views and practices.

artículo científico publicado en 2004

Increasing the acceptability and rates of organ donation among minority ethnic groups: a programme of observational and evaluative research on Donation, Transplantation and Ethnicity (DonaTE)

artículo científico publicado en 2016

Interventions that improve maternity care for immigrant women in the UK: protocol for a narrative synthesis systematic review

artículo científico

Kidney organ donation knowledge and attitudes among health care professionals: findings from a Greek general hospital

artículo científico publicado en 2012

Kidney organ donation: developing family practice initiatives to reverse inertia

artículo científico publicado en 2010

Marital status and hospital use ⬇️

artículo científico publicado el 1 de septiembre de 1977

Marital status, health, illness and service use

scientific article published on 01 December 1980

Meanings of happiness among two ethnic groups living with advanced cancer in south London: a qualitative study

artículo científico publicado en 2012

Measuring continuity of care in diabetes mellitus: an experience-based measure

artículo científico publicado en 2006

Multiple challenges for people after transitioning to secondary progressive multiple sclerosis: a qualitative study

Organ Donation and New Policies: Do We Need to Act Less Generally and More Locally?

artículo científico publicado en 2015

Organ donation attitudes and general self-efficacy: exploratory views from a rural primary care setting

scientific article published on 30 October 2019

Organ donation knowledge and attitudes among health science students in Greece: emerging interprofessional needs.

scientific article published on 25 April 2014

Parental attitudes towards the management of asthma in ethnic minorities

artículo científico publicado en 2007

Patient pressure for referral for headache: a qualitative study of GPs' referral behaviour

artículo científico publicado en 2007

Patient views on use of emergency and alternative care services for adult epilepsy: A qualitative study

artículo científico publicado en 2020

Patients' experiences of a behavioural intervention for migraine headache: a qualitative study

artículo científico publicado en 2016

Patients' perceptions and experiences of 'continuity of care' in diabetes

artículo científico publicado en 2006

Patients' perceptions of changes in their blood pressure

scientific article published on 01 April 1997

People with epilepsy obtain added value from education in groups: results of a qualitative study.

artículo científico publicado en 2017

Perceptions and experiences of epilepsy among patients from black ethnic groups in South London.

artículo científico publicado en 2014

Primary care service use by end-of-life cancer patients: a nationwide population-based cohort study in the United Kingdom

scientific article published on 29 April 2020

Promoting self-care in epilepsy: the views of patients on the advice they had received from specialists, family doctors and an epilepsy nurse

scientific article published on 01 May 1999

Psychosocial support and change in the health status of physically disabled people.

artículo científico publicado en 1986

Public knowledge and attitudes towards consent policies for organ donation in Europe. A systematic review

artículo científico publicado en 2018

Quantifying benefit-risk preferences for new medicines in rare disease patients and caregivers

artículo científico publicado en 2016

Relational and management continuity survey in patients with multiple long-term conditions

artículo científico publicado en 2010

Resisting medicines: a synthesis of qualitative studies of medicine taking

artículo científico publicado en 2005

Seizure First Aid Training For people with Epilepsy (SAFE) frequently attending emergency departments and their significant others: results of a UK multi-centre randomised controlled pilot trial

scientific article published on 16 April 2020

Self-Management education for adults with poorly controlled epILEpsy (SMILE (UK)): a randomised controlled trial protocol

artículo científico publicado en 2014

Self-Management education for adults with poorly controlled epILEpsy [SMILE (UK)]: a randomised controlled trial

Self-management education for adults with poorly controlled epilepsy (SMILE (UK)): statistical, economic and qualitative analysis plan for a randomised controlled trial

artículo científico publicado en 2015

Self-management for people with poorly controlled epilepsy: Participants' views of the UK Self-Management in epILEpsy (SMILE) program

artículo científico publicado en 2015

Service use and costs for people with headache: a UK primary care study

artículo científico publicado en 2011

Shifting towards an opt-out system in Greece: a general practice based pilot study.

artículo científico publicado en 2013

Social networks and psychosocial support among disabled people ⬇️

artículo científico publicado el 1 de enero de 1984

The effectiveness of a group self-management education course for adults with poorly controlled epilepsy, SMILE (UK): A randomized controlled trial.

artículo científico publicado en 2018

The influence of perceived medical risks and psychosocial concerns on photoprotection behaviours among adults with xeroderma pigmentosum: a qualitative interview study in the UK

scientific article published on 19 February 2019

The role of information flow between health professionals and the Child Health Computer System in the uptake of measles immunisation

article

The value of uncertainty in critical illness? An ethnographic study of patterns and conflicts in care and decision-making trajectories.

artículo científico publicado en 2016

Ultraviolet radiation exposure to the face in patients with xeroderma pigmentosum and healthy controls: applying a novel methodology to define photoprotection behaviour

Understanding kidney transplant patients' treatment choices: The interaction of emotion with medical and social influences on risk preferences.

artículo científico publicado en 2016

Using meta ethnography to synthesise qualitative research: a worked example

artículo científico publicado en 2002

Variations in lengths of stay and rates of day case surgery: implications for the efficiency of surgical management

artículo científico publicado en 1990

Vulnerability in palliative care research: findings from a qualitative study of black Caribbean and white British patients with advanced cancer.

artículo científico publicado en 2009

What are effective approaches to increasing rates of organ donor registration among ethnic minority populations: a systematic review.

artículo científico publicado en 2013

What does 'access to health care' mean?

article

What is 'continuity of care'?

Why do mothers consult when their children cough?

artículo científico publicado en 1993

Why? What? How? Using an Intervention Mapping approach to develop a personalised intervention to improve adherence to photoprotection in patients with Xeroderma Pigmentosum

Working to establish 'normality' post-transplant: a qualitative study of kidney transplant patients

artículo científico publicado en 2013

“Nudging” Deceased Donation Through an Opt-Out System: A Libertarian Approach or Manipulation?

journal article; published in The American Journal of Bioethics in 2016

Lista de obras de Myfanwy Morgan

"I know he controls cancer": the meanings of religion among Black Caribbean and White British patients with advanced cancer.

'Having a different conversation around death': diverse hospital chaplains' views on end-of-life care

'I'll be in a safe place': a qualitative study of the decisions taken by people with advanced cancer to seek emergency department care

'It doesn't do the care for you': a qualitative study of health care professionals' perceptions of the benefits and harms of integrated care pathways for end of life care

'Seizure First Aid Training' for people with epilepsy who attend emergency departments, and their family and friends: study protocol for intervention development and a pilot randomised controlled trial.

'The greatest thing in the world is the family': the meaning of social support among black Caribbean and white British patients living with advanced cancer

11.5 Ethnic minorities and indigenous peoples

A nurse-led self-management intervention for people who attend emergency departments with epilepsy: the patients' view

AN INTERVENTION TRIAL FOR PEOPLE WITH EPILEPSY ATTENDING A&E

Adjustment modes in the trajectory of progressive multiple sclerosis: a qualitative study and conceptual model

An investigation of the predictors of photoprotection and UVR dose to the face in patients with XP: a protocol using observational mixed methods.

Approaches to Photoprotection and Normalization in Highly Adherent Families of Children With Xeroderma Pigmentosum in the United Kingdom

Assessing Treatment Fidelity within an Epilepsy Randomized Controlled Trial: Seizure First Aid Training for People with Epilepsy Who Visit Emergency Departments

Attitudes to deceased organ donation and registration as a donor among minority ethnic groups in North America and the U.K.: a synthesis of quantitative and qualitative research

Attitudes to kidney donation among primary care patients in rural Crete, Greece

Attitudes to kidney donation and registering as a donor among ethnic groups in the UK

Barriers to uptake and adherence with malaria prophylaxis by the African community in London, England: focus group study

Bereaved donor families' experiences of organ and tissue donation, and perceived influences on their decision making

Changes in diet and coronary heart disease mortality among social classes in Great Britain

Continuity of care and intermediate outcomes of type 2 diabetes mellitus

Dermatology quality of life scales--a measure of the impact of skin diseases

Developing a model of short-term integrated palliative and supportive care for frail older people in community settings: perspectives of older people, carers and other key stakeholders.

Developing and assessing the acceptability of an epilepsy first aid training intervention for patients who visit UK emergency departments: A multi-method study of patients and professionals.

Developing patient-centred, feasible alternative care for adult emergency department users with epilepsy: protocol for the mixed-methods observational 'Collaborate' project

Development and evaluation of the feasibility and effects on staff, patients, and families of a new tool, the Psychosocial Assessment and Communication Evaluation (PACE), to improve communication and palliative care in intensive care and during [...]

Doctors' Interviewing Technique and Its Response to Different Booking Time

Effect of social deprivation on blood pressure monitoring and control in England: a survey of data from the quality and outcomes framework

Ethnic differences in behavioural risk factors for stroke: implications for health promotion.

Ethnicity and attitudes to deceased kidney donation: a survey in Barbados and comparison with Black Caribbean people in the United Kingdom

Ethnicity and registration as a kidney donor: the significance of identity and belonging.

Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews

Evaluating meta-ethnography: a synthesis of qualitative research on lay experiences of diabetes and diabetes care

Evaluating meta-ethnography: systematic analysis and synthesis of qualitative research

Evaluation of a personalised adherence intervention to improve photoprotection in adults with Xeroderma Pigmentosum (XP): protocol for the trial of XPAND

Experience of and access to maternity care in the UK by immigrant women: a narrative synthesis systematic review

Experience of continuity of care of patients with multiple long-term conditions in England

Experiences of food access in hospital. A new questionnaire measure

Experiences of stigma over the lifetime of people with xeroderma pigmentosum: A qualitative interview study in the United Kingdom

Explanations given by people with epilepsy for using emergency medical services: a qualitative study.

Food-related Quality of Life in Inflammatory Bowel Disease: Development and Validation of a Questionnaire.

Forms, interactions, and responses to social support: A qualitative study of support and adherence to photoprotection amongst patients with Xeroderma Pigmentosum

GPs' employment of locum doctors and satisfaction with their service.

Handwritten 'post-it' notes, questionnaire formats and response to a postal questionnaire survey

Hospital inpatients' experiences of access to food: a qualitative interview and observational study

How can a nurse intervention help people with newly diagnosed epilepsy? A qualitative study (of patients' views)

How can a nurse intervention help people with newly diagnosed epilepsy? A qualitative study of patients' views

How do patients referred to neurologists for headache differ from those managed in primary care?

Human resources policies and continuity of care

Illness doesn't belong to us ⬇️

Immigrant women's experiences of maternity-care services in Canada: a protocol for systematic review using a narrative synthesis.

Immigrant women's experiences of maternity-care services in Canada: a systematic review using a narrative synthesis.

Immigrant women's experiences of postpartum depression in Canada: a protocol for systematic review using a narrative synthesis

Implementing 'translational' biomedical research: convergence and divergence among clinical and basic scientists

Implementing the 2-week wait rule for cancer referral in the UK: general practitioners' views and practices.

Increasing the acceptability and rates of organ donation among minority ethnic groups: a programme of observational and evaluative research on Donation, Transplantation and Ethnicity (DonaTE)

Interventions that improve maternity care for immigrant women in the UK: protocol for a narrative synthesis systematic review

Kidney organ donation knowledge and attitudes among health care professionals: findings from a Greek general hospital

Kidney organ donation: developing family practice initiatives to reverse inertia

Marital status and hospital use ⬇️

Marital status, health, illness and service use

Meanings of happiness among two ethnic groups living with advanced cancer in south London: a qualitative study

Measuring continuity of care in diabetes mellitus: an experience-based measure

Multiple challenges for people after transitioning to secondary progressive multiple sclerosis: a qualitative study

Organ Donation and New Policies: Do We Need to Act Less Generally and More Locally?

Organ donation attitudes and general self-efficacy: exploratory views from a rural primary care setting

Organ donation knowledge and attitudes among health science students in Greece: emerging interprofessional needs.

Parental attitudes towards the management of asthma in ethnic minorities

Patient pressure for referral for headache: a qualitative study of GPs' referral behaviour

Patient views on use of emergency and alternative care services for adult epilepsy: A qualitative study

Patients' experiences of a behavioural intervention for migraine headache: a qualitative study

Patients' perceptions and experiences of 'continuity of care' in diabetes

Patients' perceptions of changes in their blood pressure

People with epilepsy obtain added value from education in groups: results of a qualitative study.

Perceptions and experiences of epilepsy among patients from black ethnic groups in South London.

Primary care service use by end-of-life cancer patients: a nationwide population-based cohort study in the United Kingdom

Promoting self-care in epilepsy: the views of patients on the advice they had received from specialists, family doctors and an epilepsy nurse

Psychosocial support and change in the health status of physically disabled people.

Public knowledge and attitudes towards consent policies for organ donation in Europe. A systematic review

Quantifying benefit-risk preferences for new medicines in rare disease patients and caregivers