(Q74127774)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9452071%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9452071%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

1 reference

P Julien

1

1 reference

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9 November 2019

C Gagné

2

1 reference

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9 November 2019

M R Murthy

3

1 reference

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9 November 2019

G Lévesque

4

1 reference

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9 November 2019

S Moorjani

5

1 reference

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9 November 2019

F Cadelis

6

1 reference

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9 November 2019

M R Hayden

7

1 reference

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9 November 2019

P J Lupien

8

1 reference

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9 November 2019

publication date

1 January 1998

1 reference

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9 November 2019

1 reference

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9 November 2019

volume

Suppl 1

1 reference

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9 November 2019

page(s)

S148-53

1 reference

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Relation of high-density lipoprotein cholesterol and triglycerides to incidence of atherosclerotic coronary artery disease (the PROCAM experience). Prospective Cardiovascular Münster study

9 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Detection and characterization of the heterozygote state for lipoprotein lipase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Familial combined hyperlipidemia and abnormal lipoprotein lipase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Québec

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Alterations in erythrocyte membrane lipid composition and fluidity in primary lipoprotein lipase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Molecular pathobiology of the human lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Québec

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

High density lipoprotein2. Relationship of the plasma levels of this lipoprotein species to its composition, to the magnitude of postprandial lipemia, and to the activities of lipoprotein lipase and hepatic lipase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

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

https://api.crossref.org/works/10.1002%2FHUMU.1380110150

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380110150

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9452071%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference