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Genetics of lipoprotein disorders
scientific article published on 01 September 1998
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1 reference
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Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Genetics of lipoprotein disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author name string
J Davignon
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
J Genest
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
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5 December 2019
publication date
1 September 1998
1 reference
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Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
Endocrinology and Metabolism Clinics of North America
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
521-550
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
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Low-Density Lipoprotein Subclass Patterns and Risk of Myocardial Infarction
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Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk.
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Lack of evidence for linkage between low-density lipoprotein subclass phenotypes and the apolipoprotein B locus in familial combined hyperlipidemia
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High density lipoproteins and coronary heart disease
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Familial HDL deficiency characterized by hypercatabolism of mature apoA-I but not proapoA-I
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Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a 'null' LDL-receptor gene defect
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Lp(a) concentration and apo(a) isoform size. Relation to the presence of coronary artery disease in familial hypercholesterolemia.
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Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity
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Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia.
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What benefit can be derived from treating normocholesterolemic patients with coronary artery disease?
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Myocardial infarction in the familial forms of hypertriglyceridemia
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Apoproteins B and A-I and coronary artery disease in humans.
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Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect.
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Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance
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Simvastatin improves chylomicron remnant removal in familial combined hyperlipidemia without changing chylomicron conversion.
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Postprandial apolipoprotein B100 and B48 metabolism in familial combined hyperlipidaemia before and after reduction of fasting plasma triglycerides.
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Very low density lipoprotein overproduction in genetic forms of hypertriglyceridaemia
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Adipsin/acylation stimulating protein system in human adipocytes: regulation of triacylglycerol synthesis
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Impaired response of fibroblasts from patients with hyperapobetalipoproteinemia to acylation-stimulating protein
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Modulation of Lipoprotein B Binding to the LDL Receptor by Exogenous Lipids and Apolipoproteins CI, CII, CIII, and E
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Modulation of lipoprotein(a) atherogenicity by high density lipoprotein cholesterol levels in middle-aged men with symptomatic coronary artery disease and normal to moderately elevated serum cholesterol. Regression Growth Evaluation Statin Study (RE
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Plasma lipoproteins in familial hepatic lipase deficiency
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Familial combined hyperlipidaemia: Use of stable isotopes to demonstrate overproduction of very low‐density lipoprotein apolipoprotein B by the liver
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Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and management
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Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes
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Apolipoprotein E polymorphism association with lipoprotein profile in endogenous hypertriglyceridemia and familial hypercholesterolemia
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7 January 2021
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A Phenocopy of Type III Dysbetalipoproteinemia Occurring in a Candidate Family for a Putative Apo E Receptor Defect
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Phenotypic heterogeneity associated with defective apolipoprotein B-100 and occurrence of the familial hypercholesterolemia phenotype in the absence of an LDL-receptor defect within a Canadian kindred
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Apolipoprotein E polymorphism and atherosclerosis
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based on heuristic
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Interaction of two lipid disorders in a large French-Canadian kindred.
1 reference
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Familial hypercholesterolemia in French-Canadians: taking advantage of the presence of a "founder effect".
1 reference
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Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers
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The redox status of coenzyme Q10 in total LDL as an indicator of in vivo oxidative modification. Studies on subjects with familial combined hyperlipidemia
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Prevalence and association of atherosclerosis at three different arterial sites in patients with type III hyperlipoproteinemia
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NIDDM and blood pressure as risk factors for poor cognitive performance. The Framingham Study
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Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation
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Apolipoprotein E polymorphism and heterozygous familial hypercholesterolemia. Sex-specific effects
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7 January 2021
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Genetics of type III hyperlipoproteinemia
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7 January 2021
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Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease
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Fat transport in lipoproteins--an integrated approach to mechanisms and disorders
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Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction
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Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease
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7 January 2021
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Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia
1 reference
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7 January 2021
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Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia
1 reference
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7 January 2021
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The affinity of low-density lipoproteins and of very-low-density lipoprotein remnants for the low-density lipoprotein receptor in homozygous familial defective apolipoprotein B-100
1 reference
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7 January 2021
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Fasting triglycerides, high-density lipoprotein, and risk of myocardial infarction.
1 reference
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7 January 2021
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Familial hypoalphalipoproteinemia in premature coronary artery disease
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7 January 2021
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Familial lipoprotein disorders in patients with premature coronary artery disease
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7 January 2021
based on heuristic
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Pseudo type III dyslipoproteinemia is associated with normal fibroblast lipoprotein receptor activity
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7 January 2021
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Hyperlipidemia in coronary heart disease. I. Lipid levels in 500 survivors of myocardial infarction.
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Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia
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7 January 2021
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Metabolism of apolipoprotein B in members of a family with accelerated atherosclerosis: influence of apolipoprotein E-3/E-2 pattern
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7 January 2021
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Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.
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7 January 2021
based on heuristic
inferred from DOI database lookup
Characteristics of 46 heterozygous carriers and 57 unaffected relatives in five Danish families with familial defective apolipoprotein B-100.
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperlipidemia in coronary heart disease. 3. Evaluation of lipoprotein phenotypes of 156 genetically defined survivors of myocardial infarction
1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple Genetic Determinants of Variation of Plasma Lipoproteins in Alberta Hutterites
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis and allele specific screening of apolipoprotein CIISt. Michael
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic contributions to quantitative lipoprotein traits associated with coronary artery disease: analysis of a large pedigree from the Bogalusa Heart Study
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7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
beta-Sitosterolemia with generalized eruptive xanthomatosis
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic cholesteryl ester transfer protein deficiency is extremely frequent in the Omagari area of Japan. Marked hyperalphalipoproteinemia caused by CETP gene mutation is not associated with longevity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion in the gene for the low-density-lipoprotein receptor in a majority of French Canadians with familial hypercholesterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for a dominant gene that suppresses hypercholesterolemia in a family with defective low density lipoprotein receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apolipoprotein E1-Hammersmith (Lys146-->Asn;Arg147-->Trp), due to a dinucleotide substitution, is associated with early manifestation of dominant type III hyperlipoproteinaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mouse models to study the role of APOE in hyperlipidemia and atherosclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein(a) interactions with lipid and nonlipid risk factors in early familial coronary artery disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic testing for familial hypercholesterolaemia: practical and ethical issues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Low density lipoprotein metabolism in familial combined hyperlipidemia. Mechanism of the multiple lipoprotein phenotypic expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneity of lipoprotein (a): growing complexities.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneity of plasma low-density lipoproteins and atherosclerosis risk
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein(a) in health and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elevated serum lipoprotein(a) in subclinical hypothyroidism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type III Hyperlipoproteinemia: Paradoxical Hypolipidemic Response to Estrogen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperapobetalipoproteinaemia in two families with xanthomas and phytosterolaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of hyperapobetalipoproteinemia and other lipoprotein phenotypes in men (aged < or = 50 years) and women (< or = 60 years) with coronary artery disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of apolipoprotein (a) isoform size heterogeneity as revealed by pulsed-field gel electrophoresis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lifibrol: a novel lipid-lowering drug for the therapy of hypercholesterolemia. Lifibrol Study Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phytosterolemia and pseudohomozygous type II hypercholesterolemia in two Chinese patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phytosterolaemia in a Norwegian family: diagnosis and characterization of the first Scandinavian case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phytosterolaemia: diagnosis, characterization and therapeutical approaches.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A missense mutation (Asp250→Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A major locus influencing plasma high-density lipoprotein cholesterol levels in the San Antonio Family Heart Study. Segregation and linkage analyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein (a) and coronary heart disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe familial HDL deficiency in French-Canadian kindreds. Clinical, biochemical, and molecular characterization.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cellular cholesterol transport and efflux in fibroblasts are abnormal in subjects with familial HDL deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein glomerulopathy: a pediatric case report
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolated low HDL-cholesterol as an important risk factor for coronary heart disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differences in the Phenotypic Characteristics of Subjects With Familial Defective Apolipoprotein B-100 and Familial Hypercholesterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apolipoprotein A-I deficiency. Biochemical and metabolic characteristics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decreased cholesterol biosynthesis in sitosterolemia with xanthomatosis: diminished mononuclear leukocyte 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and enzyme protein associated with increased low-density lipoprotein receptor function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular defect in hepatic cholesterol biosynthesis in sitosterolemia with xanthomatosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Family study of serum lipids and lipoproteins in coronary heart-disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of familial defective apolipoprotein B-100 in Japanese patients with familial hypercholesterolaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal lipoprotein and apolipoprotein pattern in lipoprotein glomerulopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunohistochemical analysis of spinal intradural xanthomatosis developed in a patient with phytosterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Postprandial hemorrheology and apolipoprotein B metabolism in patients with familial hypertriglyceridemia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chylomicron retention disease: exclusion of apolipoprotein B gene defects and detection of mRNA editing in an affected family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elevated Lp(a) is the most frequent familial lipoprotein disorder leading to premature myocardial infarction in a country with low cholesterol levels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene for lipoprotein lipase. A cause for low HDL cholesterol levels in individuals heterozygous for familial hypercholesterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype expression in familial combined hyperlipidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The role of apolipoprotein E genetic variants in lipoprotein disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adipose Tissue Lipoprotein Lipase and Hormone-Sensitive Lipase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired activation of adipocyte lipolysis in familial combined hyperlipidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HDL-mediated efflux of intracellular cholesterol is impaired in fibroblasts from Tangier disease patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein glomerulopathy. Report of a normolipidemic case and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical Abnormalities in Cerebrotendinous Xanthomatosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased sitosterol absorption is offset by rapid elimination to prevent accumulation in heterozygotes with sitosterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial apolipoprotein E deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous familial defective apolipoprotein B-100. Enhanced removal of apolipoprotein E-containing VLDLs and decreased production of LDLs.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel members of the low density lipoprotein receptor superfamily and their potential roles in lipid metabolism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The hypobetalipoproteinemias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Relation of serum lipoprotein(a) concentration and apolipoprotein(a) phenotype to coronary heart disease in patients with familial hypercholesterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The effect of nicotinic acid and acipimox on lipoprotein(a) concentration and turnover
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous Tangier disease and cardiovascular disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gemfibrozil and Mediterranean diet for patients with high plasma levels of lipoprotein [Lp(a)] and cholesterol--pilot study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics and molecular biology: Editorial overview
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Substrate delivery as a determinant of hepatic apoB secretion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of hyperapobetalipoproteinemia with endogenous hypertriglyceridemia and atherosclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The lowering of lipoprotein[a] induced by estrogen plus progesterone replacement therapy in postmenopausal women
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein (a) in thyroid dysfunction before and after treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The low HDL cholesterol/high triglyceride trait
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conjoint high triglycerides and low HDL cholesterol across generations. Analysis of proband hypertriglyceridemia and lipid/lipoprotein disorders in first-degree family members
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decreased resistance against in vitro oxidation of LDL from patients with familial defective apolipoprotein B-100.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Estimation of the prevalence of familial hypercholesterolaemia in a rural Afrikaner community by direct screening for three Afrikaner founder low density lipoprotein receptor gene mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A New Case of ApoA-I Deficiency Showing Codon 8 Nonsense Mutation of the ApoA-I Gene Without Evidence of Coronary Heart Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Metabolic basis of hyperapobetalipoproteinemia. Turnover of apolipoprotein B in low density lipoprotein and its precursors and subfractions compared with normal and familial hypercholesterolemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mysteries of lipoprotein(a)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in the low density lipoprotein receptor gene affect lipoprotein (a) levels: multiplicative interaction of two gene loci associated with premature atherosclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vitro lipolysis of human VLDL: effect of different VLDL compositions in normolipidemia, familial combined hyperlipidemia and familial hypertriglyceridemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atypical xanthomatosis in apolipoprotein E-deficient mice after cholesterol feeding
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normocholesterolemic tendon xanthomatosis with overproduction of apolipoprotein B
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Metformin therapy is associated with a decrease in plasma plasminogen activator inhibitor-1, lipoprotein(a), and immunoreactive insulin levels in patients with the polycystic ovary syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stable isotopes show a direct relation between VLDL apoB overproduction and serum triglyceride levels and indicate a metabolically and biochemically coherent basis for familial combined hyperlipidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic influences on lipoprotein(a) concentration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The high density lipoprotein- and apolipoprotein A-I-induced mobilization of cellular cholesterol is impaired in fibroblasts from Tangier disease subjects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uptake of type III hypertriglyceridemic VLDL by macrophages is enhanced by oxidation, especially after remnant formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Total deficiency of plasma cholesteryl ester transfer protein in subjects homozygous and heterozygous for the intron 14 splicing defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased serum remnant lipoproteins in patients with apolipoprotein E7 (apo E Suita)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serum complement and familial combined hyperlipidemia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of truncated forms of apolipoprotein B in hypobetalipoproteinemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevention of raised low-density lipoprotein cholesterol in a patient with familial hypercholesterolaemia and lipoprotein lipase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lipoprotein glomerulopathy: first report in a Chinese male
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970024-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0889-8529(05)70024-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
9785051
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9785051
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9785051%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
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