INTERIM Guidelines for the Diagnosis and Management of Familial Hypercholesterolaemia

被引:14
作者
Sullivan, David R. [1 ]
Hamilton-Craig, Ian [2 ]
van Bockxmeer, Frank [3 ]
Watts, Gerald F. [3 ]
机构
[1] Royal Prince Alfred Hosp, Dept Clin Biochem, Camperdoum, NSW 2050, Australia
[2] Griffith Univ, Dept Med, Nathan, Qld 4111, Australia
[3] Univ Western Australia, Dept Med, Royal Perth Hosp, Perth, WA 6009, Australia
关键词
Familial hypercholesterolaemia; LDL receptor mutation; Monogenic; Family cascade screening;
D O I
10.1016/j.hlc.2011.11.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:159 / 162
页数:4
相关论文
共 6 条
[1]   Guidelines for the diagnosis and management of heterozygous familial hypercholesterolemia [J].
Civeira, F .
ATHEROSCLEROSIS, 2004, 173 (01) :55-68
[2]   Integrating provision of specialist lipid services with cascade testing for familial hypercholesterolaemia [J].
Datta, Borunendra N. ;
McDowell, Ian F. W. ;
Rees, Alan .
CURRENT OPINION IN LIPIDOLOGY, 2010, 21 (04) :366-371
[3]  
Familial HypercholesterolaemiaWestern Australia Program Committee, 2008, MOD CAR FAM HYP
[4]  
HEART UK, FH GIT TOOLK
[5]  
NHS: National Institute for Health and Clinical Evidence, FAM HYP ID MAN FAM H
[6]   A New Model of Care for Familial Hypercholesterolaemia from Western Australia: Closing a Major Gap in Preventive Cardiology [J].
Watts, Gerald F. ;
van Bockxmeer, Frank M. ;
Bates, Timothy ;
Burnett, John R. ;
Juniper, Amanda ;
O'Leary, Peter .
HEART LUNG AND CIRCULATION, 2010, 19 (07) :419-422