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Results: 1 to 20 of 92

1.

Patient accounts of diagnostic testing for familial hypercholesterolaemia: comparing responses to genetic and non-genetic testing methods.

Hollands GJ, Armstrong D, Macfarlane A, Crook MA, Marteau TM.

BMC Med Genet. 2012 Sep 21;13:87. doi: 10.1186/1471-2350-13-87.

PMID:
22994377
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Screening for hypercholesterolaemia versus case finding for familial hypercholesterolaemia: a systematic review and cost-effectiveness analysis.

Marks D, Wonderling D, Thorogood M, Lambert H, Humphries SE, Neil HA.

Health Technol Assess. 2000;4(29):1-123. Review.

PMID:
11109029
[PubMed - indexed for MEDLINE]
Free Article
3.

Individuals' experiences of, and responses to, a negative genetic test result for familial hypercholesterolaemia.

Hilgart J, Mercer J, Thirlaway K.

J Health Psychol. 2013 Mar;18(3):339-49. doi: 10.1177/1359105312443403. Epub 2012 Apr 19.

PMID:
22517949
[PubMed - indexed for MEDLINE]
4.

Genetic unexceptionalism: clinician accounts of genetic testing for familial hypercholesterolaemia.

Will CM, Armstrong D, Marteau TM.

Soc Sci Med. 2010 Sep;71(5):910-7. doi: 10.1016/j.socscimed.2010.05.018. Epub 2010 Jun 4.

PMID:
20591544
[PubMed - indexed for MEDLINE]
5.

Genetic testing for familial hypercholesterolaemia: practical and ethical issues.

Humphries SE, Galton D, Nicholls P.

QJM. 1997 Mar;90(3):169-81. Review.

PMID:
9093594
[PubMed - indexed for MEDLINE]
Free Article
6.

Molecular screening for familial hypercholesterolaemia: consequences for life and disability insurance.

Homsma SJ, Huijgen R, Middeldorp S, Sijbrands EJ, Kastelein JJ.

Eur J Hum Genet. 2008 Jan;16(1):14-7. Epub 2007 Oct 24. Erratum in: Eur J Hum Genet. 2008 Feb;16(2):275.

PMID:
17957228
[PubMed - indexed for MEDLINE]
Free Article
7.

Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece.

Diakou M, Miltiadous G, Xenophontos SL, Manoli P, Cariolou MA, Elisaf M.

Eur J Intern Med. 2011 Oct;22(5):e55-9. doi: 10.1016/j.ejim.2011.01.003. Epub 2011 Feb 11.

PMID:
21925044
[PubMed - indexed for MEDLINE]
8.

Elucigene FH20 and LIPOchip for the diagnosis of familial hypercholesterolaemia: a systematic review and economic evaluation.

Sharma P, Boyers D, Boachie C, Stewart F, Miedzybrodzka Z, Simpson W, Kilonzo M, McNamee P, Mowatt G.

Health Technol Assess. 2012;16(17):1-266. doi: 10.3310/hta16170. Review.

PMID:
22469073
[PubMed - indexed for MEDLINE]
Free Article
9.

What is the clinical utility of DNA testing in patients with familial hypercholesterolaemia?

Humphries SE, Norbury G, Leigh S, Hadfield SG, Nair D.

Curr Opin Lipidol. 2008 Aug;19(4):362-8. doi: 10.1097/MOL.0b013e32830636e5. Review.

PMID:
18607183
[PubMed - indexed for MEDLINE]
10.

Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening.

Leren TP, Finborud TH, Manshaus TE, Ose L, Berge KE.

Community Genet. 2008;11(1):26-35. doi: 10.1159/000111637. Epub 2008 Jan 15.

PMID:
18196915
[PubMed - indexed for MEDLINE]
11.

Impact of genetic defects on coronary atherosclerosis in patients suspected of having familial hypercholesterolaemia.

Descamps OS, Gilbeau JP, Luwaert R, Heller FR.

Eur J Clin Invest. 2003 Jan;33(1):1-9.

PMID:
12492446
[PubMed - indexed for MEDLINE]
12.

Using the experiences of people with familial hypercholesterolaemia to help reduce the risk of cardiovascular disease: a qualitative systematic review.

Muir LA, George PM, Whitehead L.

J Adv Nurs. 2012 Sep;68(9):1920-32. doi: 10.1111/j.1365-2648.2012.05957.x. Epub 2012 Feb 20. Review.

PMID:
22348692
[PubMed - indexed for MEDLINE]
13.

Improved access to life insurance after genetic diagnosis of familial hypercholesterolaemia: cross-sectional postal questionnaire study.

Huijgen R, Homsma SJ, Hutten BA, Kindt I, Vissers MN, Kastelein JJ, van Rijckevorsel JL.

Eur J Hum Genet. 2012 Jul;20(7):722-8. doi: 10.1038/ejhg.2012.5. Epub 2012 Feb 1.

PMID:
22293687
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

[Genetic screening for familial hypercholesterolemia in 1992-1997: primarily younger patients in the care of family physicians].

ten Asbroek AH, van Lunsen S, Marang-van de Mheen PJ, Gunning-Schepers LJ.

Ned Tijdschr Geneeskd. 2000 Jan 15;144(3):125-9. Dutch.

PMID:
10674119
[PubMed - indexed for MEDLINE]
15.

Getting insurance after genetic screening on familial hypercholesterolaemia; the need to educate both insurers and the public to increase adherence to national guidelines in The Netherlands.

Marang-van de Mheen PJ, van Maarle MC, Stouthard ME.

J Epidemiol Community Health. 2002 Feb;56(2):145-7.

PMID:
11812815
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Genetic screening of patients with familial hypercholesterolaemia (FH): a New Zealand perspective.

Laurie AD, Scott RS, George PM.

Atheroscler Suppl. 2004 Dec;5(5):13-5.

PMID:
15556094
[PubMed - indexed for MEDLINE]
17.

How disturbing is it to be approached for a genetic cascade screening programme for familial hypercholesterolaemia? Psychological impact and screenees' views.

van Maarle MC, Stouthard ME, Marang-van de Mheen PJ, Klazinga NS, Bonsel GJ.

Community Genet. 2001;4(4):244-52.

PMID:
12751487
[PubMed - indexed for MEDLINE]
18.

Cost-effectiveness of a family and DNA based screening programme on familial hypercholesterolaemia in The Netherlands.

Marang-van de Mheen PJ, ten Asbroek AH, Bonneux L, Bonsel GJ, Klazinga NS.

Eur Heart J. 2002 Dec;23(24):1922-30.

PMID:
12473254
[PubMed - indexed for MEDLINE]
19.

Genetic analysis of familial hypercholesterolaemia in Western Australia.

Hooper AJ, Nguyen LT, Burnett JR, Bates TR, Bell DA, Redgrave TG, Watts GF, van Bockxmeer FM.

Atherosclerosis. 2012 Oct;224(2):430-4. doi: 10.1016/j.atherosclerosis.2012.07.030. Epub 2012 Jul 27.

PMID:
22883975
[PubMed - indexed for MEDLINE]
20.

Mutational analysis in UK patients with a clinical diagnosis of familial hypercholesterolaemia: relationship with plasma lipid traits, heart disease risk and utility in relative tracing.

Humphries SE, Cranston T, Allen M, Middleton-Price H, Fernandez MC, Senior V, Hawe E, Iversen A, Wray R, Crook MA, Wierzbicki AS.

J Mol Med (Berl). 2006 Mar;84(3):203-14. Epub 2005 Dec 31.

PMID:
16389549
[PubMed - indexed for MEDLINE]

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