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Mortality in treated heterozygous familial hypercholesterolaemia: implications for clinical management. Scientific Steering Committee on behalf of the Simon Broome Register Group.

Abstract:

Clinical management of heterozygous familial hypercholesterolaemia is largely based on evidence from a small number of observational studies and extrapolation from the results of clinical trials of lipid-lowering in patients with polygenic hypercholesterolaemia The objectives of this study were (i) to determine the absolute and relative mortality of patients with treated heterozygous familial hypercholesterolaemia, (ii) to estimate the effect of changes in treatment efficacy on mortality tren...

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Journal:
Atherosclerosis More from this journal
Volume:
142
Issue:
1
Pages:
105-112
Publication date:
1999-01-01
DOI:
EISSN:
1879-1484
ISSN:
0021-9150
Language:
English
Keywords:
Pubs id:
pubs:94960
UUID:
uuid:fe807efc-b1d5-4a61-b3dc-15a8f1913829
Local pid:
pubs:94960
Source identifiers:
94960
Deposit date:
2012-12-19

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