Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Robert Finnie"'
Autor:
Lorna McKee, William G. Simpson, Zosia Miedzybrodzka, Karen Forrest Keenan, Robert Finnie, John Dean
Publikováno v:
Journal of Community Genetics
Familial hypercholesterolemia (FH) is a serious inherited disorder, which greatly increases individuals' risk of cardiovascular disease (CVD) in adult life. However, medical treatment and lifestyle adjustments can fully restore life expectancy. Whils
Autor:
Nina Hallowell, Julia Lawton, Simon Walker, Mary Porteous, Margaret Douglas, Robert Finnie, Nicholas Jenkins
Publikováno v:
Hallowell, N, Jenkins, N, Douglas, M, Walker, S, Finnie, R, Porteous, M & Lawton, J 2016, ' A qualitative study of patients’ perceptions of the value of molecular diagnosis for familial hypercholesterolemia (FH) ', Journal of community genetics . https://doi.org/10.1007/s12687-016-0286-0
For many years, familial hypercholesterolemia (FH), an inherited disorder, has been diagnosed using phenotypic features plus family history of early onset cardiovascular disease (CVD), and has been successfully treated using statin therapy. DNA testi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e7b9ef1d8e767faf1d0cf477f16ef47
https://hdl.handle.net/20.500.11820/ab920eff-e6b3-4f0e-b81c-067f77a25f10
https://hdl.handle.net/20.500.11820/ab920eff-e6b3-4f0e-b81c-067f77a25f10
Autor:
Clement K M Ho, Robert Finnie, Sara Jenks, Christine Bell, Peter Bloomfield, Nicola Shand, Simon W Walker
Publikováno v:
The British Journal of Diabetes & Vascular Disease. 12:243-247
As in other areas of Western Europe, familial hypercholesterolaemia (FH) is one of the most frequent genetic disorders in the UK. Genetic testing for this condition is available in Scotland. This observational study describes the genetic variants fou
Autor:
Robert Finnie
Publikováno v:
The British Journal of Diabetes & Vascular Disease. 10:123-125
The publication of the UK National Institute for Health and Clinical Excellence familial hypercholesterolaemia guideline led to a combined meeting of lipidologists and geneticists in Scotland. It was agreed to implement a system of cascade screening
Autor:
Mary Porteous, Julia Lawton, Simon Walker, Nina Hallowell, Robert Finnie, Margaret Douglas, Nicholas Jenkins
Publikováno v:
Jenkins, N, Lawton, J, Douglas, M, Walker, S, Finnie, R, Porteous, M & Hallowell, N 2011, ' How do index patients participating in genetic screening programmes for familial hypercholesterolemia (FH) interpret their DNA results? A UK-based qualitative interview study ', Patient Education and Counseling, pp. 372-7 . https://doi.org/10.1016/j.pec.2011.09.002
Objective To explore patients’ interpretations of their DNA results for familial hypercholesterolemia (FH). Methods In-depth interviews were conducted with patients from two lipid clinics in Scotland, who were offered genetic testing as part of a n
Autor:
Julia Lawton, Margaret Douglas, Mary Porteous, Simon Walker, Robert Finnie, Nicholas Jenkins, Nina Hallowell
Publikováno v:
Hallowell, N, Jenkins, N, Douglas, M, Walker, S, Finnie, R, Porteous, M & Lawton, J 2011, ' Patients' experiences and views of cascade screening for familial hypercholesterolemia (FH) : a qualitative study ', Journal of community genetics, vol. 2, no. 4, pp. 249-57 . https://doi.org/10.1007/s12687-011-0064-y
Familial DNA cascade screening for familial hypercholesterolemia (FH) has recently been introduced in Scotland. This study investigated index patients' experiences of DNA testing and mediating cascade screening. Thirty-eight patients with a clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ed8dd08affb73d720793f7b9c7adca6
https://www.pure.ed.ac.uk/ws/files/8742359/Patients_experiences_and_views_of_cascade_screening_for_familial_hypercholesterolemia_FH_.pdf
https://www.pure.ed.ac.uk/ws/files/8742359/Patients_experiences_and_views_of_cascade_screening_for_familial_hypercholesterolemia_FH_.pdf
Publikováno v:
Atherosclerosis. 218:e3
Autor:
William G. Simpson, Zosia Miedzybrodzka, Robert Finnie, M. van Mourik, J. Series, Helen Gregory
Publikováno v:
Atherosclerosis. 213:e2