(Q43955454)

28 November 2017

Comparison of apolipoprotein B metabolism in familial defective apolipoprotein B and heterogeneous familial hypercholesterolemia (English)

1 reference

28 November 2017

0 references

Dairena Gaffney

1

1 reference

28 November 2017

Lorne Forster

2

1 reference

28 November 2017

Muriel J Caslake

3

1 reference

28 November 2017

Dorothy Bedford

4

1 reference

28 November 2017

J Philip Stewart

5

1 reference

28 November 2017

Grace Stewart

6

1 reference

28 November 2017

Gilbert Wieringa

7

1 reference

28 November 2017

Marek Dominiczak

8

1 reference

28 November 2017

J Paul Miller

9

1 reference

28 November 2017

Chris J Packard

10

1 reference

28 November 2017

language of work or name

1 reference

1 May 2002

1 reference

28 November 2017

1 reference

28 November 2017

162

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28 November 2017

1

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28 November 2017

33-43

1 reference

Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia

28 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and Wales

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

A World Wide Web site for low-density lipoprotein receptor gene mutations in familial hypercholesterolemia: sequence-based, tabular, and direct submission data handling.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

The metabolism of very low density and intermediate density lipoproteins in patients with familial hypercholesterolaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Increased hepatic secretion of very-low-density-lipoprotein apolipoprotein B-100 in heterozygous familial hypercholesterolaemia: a stable isotope study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Homozygous familial defective apolipoprotein B-100. Enhanced removal of apolipoprotein E-containing VLDLs and decreased production of LDLs.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Rapid testing for three mutations causing familial defective apolipoprotein B100 in 562 patients with familial hypercholesterolaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

Metabolism of apolipoprotein B in large triglyceride-rich very low density lipoproteins of normal and hypertriglyceridemic subjects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2801%2900679-7

10.1016/S0021-9150(01)00679-7

7 January 2021

Identifiers

DOI

1 reference

28 November 2017

1 reference