6th Hellenic Congress in Athens, of the Hellenic Atherosclerosis Society, on the 04-06 December 2014 Novel Pharmacologic Treatments of Familial Hypercholesterolaemia

Familial hypercholesterolaemia (FH) is the most common inherited monogenic lipid disorder. It is caused by mutations of genes related to low density lipoprotein (LDL) receptors, apolipoprotein B or proprotein convertase subtilisin/kexin type 9 (PCSK9). Homozygous FH (HoFH; 1/400,000 births) is treat...

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Detalles Bibliográficos
Autor principal: Athyros, VG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645966/
https://www.ncbi.nlm.nih.gov/pubmed/26664657
http://dx.doi.org/10.2174/1874192401509010073

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645966/
https://www.ncbi.nlm.nih.gov/pubmed/26664657
http://dx.doi.org/10.2174/1874192401509010073

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