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Guidelines for Diagnosis and Treatment of Familial Hypercholesterolemia 2017
1. Familial hypercholesterolemia (FH) is an autosomal hereditary disease with the 3 major clinical features of hyper-LDL-cholesterolemia, premature coronary artery disease and tendon and skin xanthomas. As there is a considerably high risk of coronary artery disease (CAD), in addition to early diagn...
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| Gepubliceerd in: | J Atheroscler Thromb |
|---|---|
| Hoofdauteurs: | , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Japan Atherosclerosis Society
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6099072/ https://ncbi.nlm.nih.gov/pubmed/29877295 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5551/jat.CR003 |
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