Pages that link to "Q40562181"
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The following pages link to Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington's disease. (Q40562181):
Displaying 50 items.
- Mood disorders in Huntington's disease: from behavior to cellular and molecular mechanisms (Q21131050) (← links)
- Huntington's disease (Q28284355) (← links)
- Suicidal ideation in Huntington disease: the role of comorbidity (Q30416862) (← links)
- Predictive testing for inherited prion disease: report of 22 years experience (Q33882164) (← links)
- Misunderstandings concerning genetics among patients confronting genetic disease (Q34154652) (← links)
- Long-term outcome of presymptomatic testing in Huntington disease (Q34325599) (← links)
- "Am I carrier?" The patient's lived experience of thrombophilia genetic screening and its outcome (Q35136009) (← links)
- Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review. (Q35446354) (← links)
- Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions (Q36050548) (← links)
- Depression in the early stages of Huntington disease (Q36197669) (← links)
- Emerging empirical evidence on the ethics of schizophrenia research (Q36291530) (← links)
- It's "back to school" for genetic screening (Q36396732) (← links)
- Why tell asymptomatic children of the risk of an adult-onset disease in the family but not test them for it? (Q36639335) (← links)
- Grading quality of evidence and strength of recommendations for diagnostic tests and strategies (Q36661809) (← links)
- Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease (Q36820946) (← links)
- Critiques of the risk concept--valid or not? (Q36939706) (← links)
- Characterization of depression in prodromal Huntington disease in the neurobiological predictors of HD (PREDICT-HD) study (Q37254698) (← links)
- Economic methods for valuing the outcomes of genetic testing: beyond cost-effectiveness analysis (Q37315305) (← links)
- A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases (Q37323166) (← links)
- Factors associated with experiences of genetic discrimination among individuals at risk for Huntington disease (Q37386039) (← links)
- Evaluation of the Validity and Utility of Genetic Testing for Rare Diseases (Q37786243) (← links)
- The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature (Q38252488) (← links)
- Patient reported outcomes and patient empowerment in clinical genetics services (Q38259348) (← links)
- Genetic counseling and testing for Huntington's disease: A historical review (Q38833267) (← links)
- Adherence to the breast cancer surveillance program for women at risk for familial breast and ovarian cancer versus overscreening: a monocenter study in Germany (Q39934142) (← links)
- Long-term monitoring of the mortality trend of Huntington's disease in Austria (Q40435328) (← links)
- DNA: where to now? (Q41842055) (← links)
- Recent advances in the management of choreas (Q42143817) (← links)
- Recommendations for the predictive genetic test in Huntington's disease (Q43453202) (← links)
- Short-term psychological impact of predictive testing for Machado-Joseph disease: depression and anxiety levels in individuals at risk from the Azores (Portugal). (Q43608814) (← links)
- Why do they do it? A pilot study towards understanding participant motivation and experience in a large genetic epidemiological study of endometriosis (Q44710449) (← links)
- Providing predictive testing for Huntington disease via telehealth: results of a pilot study in British Columbia, Canada (Q45290171) (← links)
- Genetic testing and Huntington's disease: issues of employment (Q45292968) (← links)
- Partners of mutation-carriers for Huntington's disease: forgotten persons? (Q45297425) (← links)
- Predictive genetic test decisions for Huntington's disease: elucidating the test/no-test dichotomy (Q45297616) (← links)
- An international survey of predictive genetic testing in children for adult onset conditions (Q45297686) (← links)
- The Confluence of Psychiatric Symptoms and Neurodegenerative Disease: Impact on Genetic Counseling. (Q45299786) (← links)
- More Appreciation of Life or Regretting the Test? Experiences of Living as a Mutation Carrier of Huntington's Disease (Q45299882) (← links)
- Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease (Q45305832) (← links)
- Ethical issues in neurogenetics (Q47560820) (← links)
- The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life (Q47570840) (← links)
- Genetics Health Professionals' Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late-Onset Neurological Diseases in Portugal: Core Components, Specific Challenges and the Need for Assessment Tools (Q47713917) (← links)
- Female Sexual Dysfunction in Presymptomatic Mutation Carriers and Patients with Huntington's Disease (Q47770556) (← links)
- Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba. (Q48412678) (← links)
- Mothers' appreciation of chromosomal microarray analysis for autism spectrum disorder (Q50310101) (← links)
- Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: assessment of anxiety, depression, and perception of health (Q50954326) (← links)
- Diagnostic accuracy and linked evidence--testing the chain (Q51186192) (← links)
- What to Do with a Second Chance in Life? Long-Term Experiences of Non-carriers of Huntington's Disease. (Q52601552) (← links)
- Subtle Psychosocial Sequelae of Genetic Test Results (Q57778792) (← links)
- Role of the Disease in the Psychological Impact of Pre-Symptomatic Testing for SCA2 and FAP ATTRV30M: Experience with the Disease, Kinship and Gender of the Transmitting Parent (Q57949853) (← links)