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Clinical Lipidology
Article . 2013 . Peer-reviewed
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https://dx.doi.org/10.2217/clp...
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Homozygous familial hypercholesterolemia

descriptionPublicationkeyboard_double_arrow_right Article 01 Aug 2013 English Publisher:Informa UK LimitedJournal:Clinical Lipidology, volume 8, pages 407-409 (issn: 1758-4299, eissn: 1758-4302, Copyright policy )
Authors: Anthony S Wierzbicki;

doi: 10.2217/clp.13.37

Homozygous familial hypercholesterolemia

Abstract

Evaluation of: Rocha VZ, Chacra AP, Salgado W et al. Extensive xanthomata and severe subclinical atherosclerosis in homozygous familial hypercholesterolemia. J. Am. Coll. Cardiol. 61(21), 2193 (2013).This paper evaluation summarizes a case report of homozygous familial hypercholesterolemia. The patient in this particular case presented with gross xanthomata, elevated LDL cholesterol and extant coronary arterial disease in early adulthood. The clinical diagnosis, physical signs and management of the condition are discussed and future treatment options for homozygous familial hypercholesterolemia are reviewed.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
1
Average
Average
Average
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