Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease
about
Perception, experience, and response to genetic discrimination in Huntington disease: the international RESPOND-HD studyPotential stigma associated with inclusion of the psychosis risk syndrome in the DSM-V: an empirical questionPersonal factors associated with reported benefits of Huntington disease family history or genetic testing.Onset of Huntington's disease: can it be purely cognitive?The role of disease perceptions and results sharing in psychological adaptation after genetic susceptibility testing: the REVEAL StudyParental attitudes, beliefs, and perceptions about genetic testing for FAP and colorectal cancer surveillance in minors.In their own words: reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND-HD study.The influence of medical testing on patients' health: an overview from the gynecologists' perspective.Spontaneous disclosure of BRCA1/2 genetic test results to employers: a French prospective studyPerception, experience, and response to genetic discrimination in Huntington's disease: the Australian results of The International RESPOND-HD study.Couples' attributions for work function changes in prodromal Huntington diseaseLegal update: living with the Genetic Information Nondiscrimination ActCivilian and military genetics: nondiscrimination policy in a post-GINA world.Caregiving by teens for family members with Huntington disease.Neuroprotection for Huntington's disease: ready, set, slowThe emotional experiences of family carers in Huntington disease.Huntington disease: families' experiences of healthcare servicesFactors associated with experiences of genetic discrimination among individuals at risk for Huntington disease.Early Detection of Huntington Disease.Ethical issues of predictive genetic testing for diabetes.Global trends on fears and concerns of genetic discrimination: a systematic literature review.Policy framework for rare disease health disparities.Analysis of the Reasons for Non-Uptake of Predictive Testing for Huntington's Disease in Spain: A Qualitative Study.Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act.Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington disease.Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease.Exploring quality of life in Italian patients with rare disease: a computer-aided content analysis of illness stories.The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life.
P2860
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P2860
Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease
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
Perceptions of discrimination ...... sting for Huntington's disease
@en
type
label
Perceptions of discrimination ...... sting for Huntington's disease
@en
prefLabel
Perceptions of discrimination ...... sting for Huntington's disease
@en
P2093
P2860
P50
P356
P1476
Perceptions of discrimination ...... sting for Huntington's disease
@en
P2093
Anne Wallis
Cheryl Erwin
Elizabeth Penziner
Leigh J Beglinger
Yvonne Bombard
P2860
P304
P356
10.1002/AJMG.B.30600
P577
2008-04-01T00:00:00Z