Familial hypoalphalipoproteinemia in premature coronary artery disease

scientific article published on 01 December 1993

Familial hypoalphalipoproteinemia in premature coronary artery disease is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1161/01.ATV.13.12.1728
P698PubMed publication ID8241092

P2093author name stringE J Schaefer
J M Ordovas
J Genest
J C Fruchart
J M Bard
P433issue12
P921main subjectcoronary artery diseaseQ844935
hypoalphalipoproteinemiaQ5959167
P304page(s)1728-1737
P577publication date1993-12-01
P1433published inArteriosclerosis and thrombosis : a journal of vascular biologyQ27709770
P1476titleFamilial hypoalphalipoproteinemia in premature coronary artery disease
P478volume13

Reverse relations

cites work (P2860)
Q37288388A diagnostic algorithm for the atherogenic apolipoprotein B dyslipoproteinemias.
Q44205520A low high density lipoprotein (HDL) level is associated with carotid artery intima-media thickness in asymptomatic members of low HDL families
Q74341167Alterations in the main steps of reverse cholesterol transport in male patients with primary hypertriglyceridemia and low HDL-cholesterol levels
Q37576113ApoB versus non-HDL-C: what to do when they disagree
Q28351795Apolipoprotein B versus lipoprotein lipids: vital lessons from the AFCAPS/TexCAPS trial
Q37835397Clinical presentation, laboratory values, and coronary heart disease risk in marked high-density lipoprotein-deficiency states.
Q40440943Clustering of cardiovascular risk factors: Targeting high-risk individuals
Q44329447Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol
Q74348218Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations
Q28067479Diagnosis and treatment of high density lipoprotein deficiency
Q31018798Discovery of biomarker candidates for coronary artery disease from an APOE-knock out mouse model using iTRAQ-based multiplex quantitative proteomics.
Q44300074Effects on apoB-100 secretion and bile acid synthesis by redirecting cholesterol efflux from HepG2 cells
Q24608464Evaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guideline
Q24792755Gene therapy for lipid disorders
Q58545602Genetic and secondary causes of severe HDL deficiency and cardiovascular disease
Q33993060Genetic causes of high and low serum HDL-cholesterol
Q77452737Genetics of lipoprotein disorders
Q37000080HDL metabolism and the role of HDL in the treatment of high-risk patients with cardiovascular disease
Q34107511High-density lipoprotein metabolism: molecular targets for new therapies for atherosclerosis
Q35856884High-density lipoprotein subfractions and risk of coronary artery disease
Q34990624High-density lipoproteins and atherosclerosis
Q28645890How, when, and why to use apolipoprotein B in clinical practice
Q51552490Hypercholesterolemia and Dyslipidemia.
Q51537186Hypercholesterolemia and Dyslipidemia: Issues for the Clinician.
Q54053962Impaired HDL response to fat in men with coronary artery disease.
Q77452740Lipoproteins and atherogenesis
Q22010457Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
Q46684197Prevalence of obesity and its association with cardiovascular disease risk factors in adolescent girls from a college in central Taiwan
Q34003407Preventing, stopping, or reversing coronary artery disease--triglyceride-rich lipoproteins and associated lipoprotein and metabolic abnormalities: the need for recognition and treatment
Q36901653Primary Low Level of High-Density Lipoprotein Cholesterol and Risks of Coronary Heart Disease, Cardiovascular Disease, and Death: Results From the Multi-Ethnic Study of Atherosclerosis
Q80231409Reference distributions for apolipoproteins AI and B and B/AI ratios: comparison of a large cohort to the world's literature
Q33310999Sphingomyelin phosphodiesterase-1 (SMPD1) coding variants do not contribute to low levels of high-density lipoprotein cholesterol
Q52595882The Design and Rationale of SAVE BC: The Study to Avoid Vascular Events in British Columbia.
Q73112125The replacement of arginine by cysteine at residue 151 in apolipoprotein A-I produces a phenotype similar to that of apolipoprotein A-IMilano
Q37049629The strengths and limitations of the apoB/apoA-I ratio to predict the risk of vascular disease: a Hegelian analysis

Search more.