Literature DB >> 4188273

Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states.

J Slack.   

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Year:  1969        PMID: 4188273     DOI: 10.1016/s0140-6736(69)90930-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  118 in total

1.  Extent of underdiagnosis of familial hypercholesterolaemia in routine practice: prospective registry study.

Authors:  H A Neil; T Hammond; R Huxley; D R Matthews; S E Humphries
Journal:  BMJ       Date:  2000-07-15

2.  Editorial: Early prevention of atherosclerosis.

Authors:  J P Kane; M J Malloy
Journal:  West J Med       Date:  1975-04

Review 3.  Role of lipid-lowering pharmacotherapy in children.

Authors:  S Tonstad
Journal:  Paediatr Drugs       Date:  2000 Jan-Feb       Impact factor: 3.022

4.  Improved access to life insurance after genetic diagnosis of familial hypercholesterolaemia: cross-sectional postal questionnaire study.

Authors:  Roeland Huijgen; Sietske J M Homsma; Barbara A Hutten; Iris Kindt; Maud N Vissers; John J P Kastelein; Jan L A van Rijckevorsel
Journal:  Eur J Hum Genet       Date:  2012-02-01       Impact factor: 4.246

5.  Can drug therapy alter the natural course of peripheral vascular disease?: a review.

Authors:  C A Clyne
Journal:  Proc R Soc Med       Date:  1977

Review 6.  Hyperlipidaemia in children.

Authors:  J K Lloyd
Journal:  Br Heart J       Date:  1975-02

7.  Family similarities in the age at coronary death in familial hypercholesterolaemia.

Authors:  A Heiberg; J Slack
Journal:  Br Med J       Date:  1977-08-20

Review 8.  Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology?

Authors:  Shah Ebrahim; George Davey Smith
Journal:  Hum Genet       Date:  2007-11-23       Impact factor: 4.132

9.  Use of the single-strand conformational polymorphism method to detect recurrent and novel mutations in the low-density lipoprotein receptor gene in patients with familial hypercholesterolaemia: detection of a novel mutation Asp200-->Gly.

Authors:  V Gudnason; Y T Mak; J Betteridge; S N McCarthy; S Humphries
Journal:  Clin Investig       Date:  1993-04

10.  Coronary artery disease and haemostatic variables in heterozygous familial hypercholesterolaemia.

Authors:  D D Sugrue; I Trayner; G R Thompson; V J Vere; J Dimeson; Y Stirling; T W Meade
Journal:  Br Heart J       Date:  1985-03
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