Reduction in Mortality in Subjects With Homozygous Familial Hypercholesterolemia Associated With Advances in Lipid-Lowering Therapy

Author:

Raal Frederick J.1,Pilcher Gillian J.1,Panz Vanessa R.1,van Deventer Hendrick E.1,Brice Brigitte C.1,Blom Dirk J.1,Marais A. David1

Affiliation:

1. From the Carbohydrate & Lipid Metabolism Research Unit, Department of Medicine (F.J.R., G.J.P., V.R.P.), and the Department of Chemical Pathology (H.E.v.D.), University of the Witwatersrand, Johannesburg, South Africa; and Division of Lipidology, Department of Medicine, University of Cape Town, Cape Town, South Africa (B.C.B., D.J.B., A.D.M.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference32 articles.

1. Monogenic hypercholesterolemia: new insights in pathogenesis and treatment

2. A host of hypercholesterolaemic homozygotes in South Africa.

3. Three mutations that cause familial hypercholesterolemia in Afrikaners identified: a milestone in South African medicine;Gevers W;S Afr Med J,1989

4. Lowering LDL--Not Only How Low, But How Long?

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