Parents’ views of genetic testing and treatment of familial hypercholesterolemia in children: a qualitative study
Author:
Funder
Chief Scientist Office
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Public Health, Environmental and Occupational Health,Epidemiology
Link
http://link.springer.com/article/10.1007/s12687-018-0373-5/fulltext.html
Reference56 articles.
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2. Brice P, Burton H, Edwards CW, Humphries SE, Aitman TJ (2013) Familial hypercholesterolaemia: a pressing issue for European healthcare. Atherosclerosis 231:223–226
3. Burton H (2011) Genetics and mainstream medicine: service development and integration. Public Health Genetics Foundation, Cambridge
4. Chapple A, May C, Campion P (1996) Predictive and carrier testing of children: professional dilemmas for clinical geneticists. Hum Reproduc & Gen Ethics 2:28–37
5. Claassen L, Henneman L, Kindt I, Marteau TM, Timmermans DR (2010) Perceived risk and representations of cardiovascular disease and preventive behaviour in people diagnosed with familial hypercholesterolemia: a cross-sectional questionnaire study. J Health Psychol 15:33–43
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3. Treatment of pediatric heterozygous familial hypercholesterolemia 7 years after the EAS recommendations: Real-world results from a large French cohort;Archives de Pédiatrie;2024-04
4. Promoting Holistic Care in Familial Hypercholesterolemia;Journal of Cardiovascular Nursing;2023-05-19
5. Factors Predicting Statin Initiation During Childhood in Familial Hypercholesterolemia: Importance of Genetic Diagnosis;The Journal of Pediatrics;2023-02
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