Lipoprotein(a) levels in patients with homozygous familial hypercholesterolaemia

Atherosclerosis

Volumn 157, Issue 1, 2001, Pages 255-256

  Miltiadous, George ^a   Tsimihodimos, Vasilios ^a   Bairaktari, Eleni ^a   Elisaf, Moses ^a  

^a UNIVERSITY OF IOANNINA   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ANTILIPEMIC AGENT; APOLIPOPROTEIN A; LIPOPROTEIN A; LOW DENSITY LIPOPROTEIN RECEPTOR;

ALLELE; CELL MEMBRANE; CELL SURFACE; CHOLESTEROL BLOOD LEVEL; CLINICAL FEATURE; FAMILIAL HYPERCHOLESTEROLEMIA; FATTY ACID METABOLISM; GENE FREQUENCY; GENE MUTATION; GENETIC DISORDER; HUMAN; LETTER; LIGAND BINDING; LIPOPROTEIN BLOOD LEVEL; LIPOPROTEIN SYNTHESIS; PRIORITY JOURNAL; PROTEIN DEGRADATION; RECEPTOR GENE;

FEMALE; HOMOZYGOTE; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; LIPOPROTEIN(A); MALE;

EID: 0034971292     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-9150(01)00536-6     Document Type: Letter

References (7)

1. Familial hypercholesterolaemia
2. Lp(a) levels in Greek patients with heterozygous familial hypercholesterolemia
3. Lipoprotein(a) in homozygous familial hypercholesterolaemia
4. Apolipoprotein (a) synthesis and secretion from hepatoma cells is coupled to triglyceride synthesis and secretion
5. De novo production of low density lipoprotein: Fact or fancy
6. The LDL receptor locus and familial hypercholesterolemia: Mutational analysis of a membrane protein
7. Lipoprotein Lp(a) in homozygous familial hypercholesterolaemia: Density profile, particle heterogeneity and apolipoprotein(a) phenotype