Atherosclerosis
- CARNEIRO MM
, Miname MH, Gagliardi AC, Pereira C, et al
The removal from plasma of chylomicrons and remnants is reduced in heterozygous
familial hypercholesterolemia subjects with identified LDL receptor mutations:
Study with artificial emulsions.
Atherosclerosis. 2011.
PubMed
Text format
Related articles
Abstract available

- PALACIOS L
, Grandoso L, Cuevas N, Olano-Martin E, et al
Molecular characterization of familial hypercholesterolemia in Spain.
Atherosclerosis. 2011.
PubMed
Text format
Related articles
Abstract available

J Intern Med
- SURENDRAN RP
, Visser ME, Heemelaar S, Wang J, et al
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe
hypertriglyceridaemia.
J Intern Med. 2012 Jan 12. doi: 10.1111/j.1365-2796.2012.02516.
PubMed
Text format
Related articles
Abstract available
