Lista de obras - Fiona Ulph - Dominio Público Uruguay

A qualitative study exploring genetic counsellors' experiences of counselling children

artículo científico publicado en 2010

A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status

artículo científico publicado en 2015

An exploration of parents' perceptions and beliefs about changes following participation in a family skill training program: a qualitative study in a developing country

artículo científico publicado en 2015

Cognitive-behavioural suicide prevention for male prisoners: a pilot randomized controlled trial.

artículo científico publicado en 2015

Communicating Carrier Status Information to Children: Their Ability to Understand Concepts Related to Genetic Testing

Communication of carrier status information following universal newborn screening for sickle cell disorders and cystic fibrosis: qualitative study of experience and practice

artículo científico publicado en 2009

Communication with children about sickle cell disease: A qualitative study of parent experience

article by Joanne Middleton et al published 9 June 2018 in British Journal of Health Psychology

Consent for newborn screening: screening professionals' and parents' views

scientific article published on 04 November 2019

Constructing a Bioethical Framework to Evaluate and Optimise Newborn Bloodspot Screening for Cystic Fibrosis

artículo científico publicado en 2020

Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

artículo científico publicado en 2015

Disparities in current and future childhood and newborn carrier identification

artículo científico publicado en 2014

Effect of hopelessness on the links between psychiatric symptoms and suicidality in a vulnerable population at risk of suicide

artículo científico publicado en 2015

Eliciting Preferences for Information Provision in Newborn Bloodspot Screening Programs

artículo científico publicado en 2017

Ethical issues in research into conflict and displacement

artículo científico publicado en 2013

Exploration of Mechanisms behind Changes after Participation in a Parenting Intervention: A Qualitative Study in a Low-Resource Setting

artículo científico

Familial influences on antenatal and newborn haemoglobinopathy screening

article

How should risk be communicated to children: a cross-sectional study comparing different formats of probability information.

artículo científico publicado en 2009

Imparting carrier status results detected by universal newborn screening for sickle cell and cystic fibrosis in England: a qualitative study of current practice and policy challenges

artículo científico publicado en 2007

Improving the quality of prison research: A qualitative study of ex-offender service user involvement in prison suicide prevention research

artículo científico

Informing children of their newborn screening carrier result for sickle cell or cystic fibrosis: qualitative study of parents' intentions, views and support needs.

artículo científico publicado en 2013

PINSA (Provision of Information about Newborn Screening Antenatally): The Provision of antenatal Information for the NHS Newborn Bloodspot Screening Programme (NBSP)

Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening

artículo científico publicado en 2014

Personality functioning: the influence of stature

artículo científico publicado en 2004

Preventing interpersonal violence in Panama: is a parenting intervention developed in Australia culturally appropriate?

artículo científico publicado en 2016

Provision of information about newborn screening antenatally: a sequential exploratory mixed-methods project

artículo científico publicado en 2017

Psychological Impact on Parents of an Inconclusive Diagnosis Following Newborn Bloodspot Screening for Cystic Fibrosis: A Qualitative Study

scientific article published on 11 June 2019

Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research

publication published on 08 March 2022

Risks and benefits of nanotechnology: How young adults perceive possible advances in nanomedicine compared with conventional treatments

scholarly article by Brigitte Nerlich et al published June 2007 in Health Risk & Society

The Role of Information Provision in Economic Evaluations of Newborn Bloodspot Screening: A Systematic Review

artículo científico publicado en 2015

The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani women

artículo científico publicado en 2020

The moderating effects of coping and self-esteem on the relationship between defeat, entrapment and suicidality in a sample of prisoners at high risk of suicide.

artículo científico publicado en 2015

The prioritization of symptom beliefs over illness beliefs: The development and validation of the Pain Perception Questionnaire for Young People

artículo científico publicado en 2017

Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups

artículo científico publicado en 2016

Young adults' pre-existing knowledge of cystic fibrosis and sickle cell diseases: implications for newborn screening

artículo científico publicado en 2013

Young children's experiences of living with a parent with bipolar disorder: Understanding the child's perspective

artículo científico publicado en 2016

Lista de obras de Fiona Ulph

A qualitative study exploring genetic counsellors' experiences of counselling children

A qualitative study to explore how professionals in the United Kingdom make decisions to test children for a sickle cell carrier status

An exploration of parents' perceptions and beliefs about changes following participation in a family skill training program: a qualitative study in a developing country

Cognitive-behavioural suicide prevention for male prisoners: a pilot randomized controlled trial.

Communicating Carrier Status Information to Children: Their Ability to Understand Concepts Related to Genetic Testing

Communication of carrier status information following universal newborn screening for sickle cell disorders and cystic fibrosis: qualitative study of experience and practice

Communication with children about sickle cell disease: A qualitative study of parent experience

Consent for newborn screening: screening professionals' and parents' views

Constructing a Bioethical Framework to Evaluate and Optimise Newborn Bloodspot Screening for Cystic Fibrosis

Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

Disparities in current and future childhood and newborn carrier identification

Effect of hopelessness on the links between psychiatric symptoms and suicidality in a vulnerable population at risk of suicide

Eliciting Preferences for Information Provision in Newborn Bloodspot Screening Programs

Ethical issues in research into conflict and displacement

Exploration of Mechanisms behind Changes after Participation in a Parenting Intervention: A Qualitative Study in a Low-Resource Setting

Familial influences on antenatal and newborn haemoglobinopathy screening

How should risk be communicated to children: a cross-sectional study comparing different formats of probability information.

Imparting carrier status results detected by universal newborn screening for sickle cell and cystic fibrosis in England: a qualitative study of current practice and policy challenges

Improving the quality of prison research: A qualitative study of ex-offender service user involvement in prison suicide prevention research

Informing children of their newborn screening carrier result for sickle cell or cystic fibrosis: qualitative study of parents' intentions, views and support needs.

PINSA (Provision of Information about Newborn Screening Antenatally): The Provision of antenatal Information for the NHS Newborn Bloodspot Screening Programme (NBSP)

Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening

Personality functioning: the influence of stature

Preventing interpersonal violence in Panama: is a parenting intervention developed in Australia culturally appropriate?

Provision of information about newborn screening antenatally: a sequential exploratory mixed-methods project

Psychological Impact on Parents of an Inconclusive Diagnosis Following Newborn Bloodspot Screening for Cystic Fibrosis: A Qualitative Study

Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research

Risks and benefits of nanotechnology: How young adults perceive possible advances in nanomedicine compared with conventional treatments

The Role of Information Provision in Economic Evaluations of Newborn Bloodspot Screening: A Systematic Review

The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani women

The moderating effects of coping and self-esteem on the relationship between defeat, entrapment and suicidality in a sample of prisoners at high risk of suicide.

The prioritization of symptom beliefs over illness beliefs: The development and validation of the Pain Perception Questionnaire for Young People

Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups

Young adults' pre-existing knowledge of cystic fibrosis and sickle cell diseases: implications for newborn screening

Young children's experiences of living with a parent with bipolar disorder: Understanding the child's perspective