about
Ethical issues associated with genetic counseling in the context of adolescent psychiatryEmpowerment of Cancer Survivors Through Information Technology: An Integrative ReviewPoints to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocolCollating the knowledge base for core outcome set development: developing and appraising the search strategy for a systematic review.Patient empowerment: the need to consider it as a measurable patient-reported outcome for chronic conditions.Empowerment: qualitative underpinning of a new clinical genetics-specific patient-reported outcomeOwnership of uncertainty: healthcare professionals counseling and treating women from hereditary breast and ovarian cancer families who receive an inconclusive BRCA1/2 genetic test resultEvaluating a unique, specialist psychiatric genetic counseling clinic: uptake and impactA prospective cohort study assessing clinical referral management & workforce allocation within a UK regional medical genetics service.Deaf genetic testing and psychological well-being in deaf adults.Non-invasive prenatal testing for single gene disorders: exploring the ethics.Patient reported outcomes and patient empowerment in clinical genetics services.Defining Our Clinical Practice: The Identification of Genetic Counseling Outcomes Utilizing the Reciprocal Engagement Model.Non-invasive Prenatal Diagnosis for BRCA Mutations - a Qualitative Pilot Study of Health Professionals' Views.Patient expectations and attitudes towards specialist genetic eye services.Experiences of Women Who Underwent Predictive BRCA 1/2 Mutation Testing Before the Age of 30.Understanding the expectations of patients with inherited retinal dystrophies.Empowerment beliefs and intention to uptake cervical cancer screening: three psychosocial mediating mechanisms.Valuing Preferences for the Process and Outcomes of Clinical Genetics Services: A Pilot Study.Identifying outcomes of clinical genetic services: qualitative evidence and methodological considerations.Communication about DTC testing: commentary on a 'family experience of personal genomics'.Making sense of risk diagnosis in case of prenatal and reproductive genetic counselling for neuromuscular diseases.Genetic testing: when prediction generates stigmatization.Valuing the economic benefits of complex interventions: when maximising health is not sufficient.Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.Translation and Cross-Cultural Adaptation with Preliminary Validation of GCOS-24 for Use in Spain.Reproductive empowerment: the main motivator and outcome of carrier testing.Development of FOCUS-GC: Framework for Outcomes of Clinical Communication Services in Genetic Counseling.The Genetic Counseling Outcome Scale: a new patient-reported outcome measure for clinical genetics services.Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services.Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire.Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network.Measuring outcomes in aphasia research: A review of current practice and an agenda for standardisation
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Patient empowerment in clinical genetics services.
@en
type
label
Patient empowerment in clinical genetics services.
@en
prefLabel
Patient empowerment in clinical genetics services.
@en
P2860
P50
P356
P1476
Patient empowerment in clinical genetics services
@en
P2093
Dian Donnai
Rhona Macleod
P2860
P304
P356
10.1177/1359105308095063
P577
2008-10-01T00:00:00Z