Shoulders CC - Search Results

1

Family history in first degree relatives of patients with premature cardiovascular disease.

Andreotti F, Crea F, Patti G, Shoulders CC, Navarese EP, Robishaw J, Maseri A, Hennekens CH. Andreotti F, et al. Among authors: shoulders cc. Int J Cardiol. 2021 Jun 15;333:215-218. doi: 10.1016/j.ijcard.2021.03.026. Epub 2021 Mar 15. Int J Cardiol. 2021. PMID: 33737169

2

Risk factors in schoolchildren associated with a family history of unheralded myocardial infarction or uncomplicated stable angina in male relatives.

Crea F, Gaspardone A, Tomai F, Shoulders C, De Fazio A, Versaci F, Iamele M, Roncaglioni C, Gioffré M, Maseri A, et al. Crea F, et al. J Am Coll Cardiol. 1994 May;23(6):1472-8. doi: 10.1016/0735-1097(94)90394-8. J Am Coll Cardiol. 1994. PMID: 8176109 Free article.

3

HEART UK consensus statement on Lipoprotein(a): A call to action.

Cegla J, Neely RDG, France M, Ferns G, Byrne CD, Halcox J, Datta D, Capps N, Shoulders C, Qureshi N, Rees A, Main L, Cramb R, Viljoen A, Payne J, Soran H; HEART UK Medical, Scientific and Research Committee. Cegla J, et al. Atherosclerosis. 2019 Dec;291:62-70. doi: 10.1016/j.atherosclerosis.2019.10.011. Epub 2019 Oct 14. Atherosclerosis. 2019. PMID: 31704552 Free article. Review.

4

Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children.

Shoulders CC, Grantham TT, North JD, Gaspardone A, Tomai F, de Fazio A, Versaci F, Gioffre PA, Cox NJ. Shoulders CC, et al. Hum Genet. 1996 Nov;98(5):557-66. doi: 10.1007/s004390050259. Hum Genet. 1996. PMID: 8882875

5

HEART UK statement on the management of homozygous familial hypercholesterolaemia in the United Kingdom.

France M, Rees A, Datta D, Thompson G, Capps N, Ferns G, Ramaswami U, Seed M, Neely D, Cramb R, Shoulders C, Barbir M, Pottle A, Eatough R, Martin S, Bayly G, Simpson B, Halcox J, Edwards R, Main L, Payne J, Soran H; for HEART UK Medical Scientific and Research Committee. France M, et al. Atherosclerosis. 2016 Dec;255:128-139. doi: 10.1016/j.atherosclerosis.2016.10.017. Epub 2016 Nov 5. Atherosclerosis. 2016. PMID: 27839699 Free article. Review.

6

Corrigendum to "HEART UK consensus statement on Lipoprotein(a): A call to action" [Atherosclerosis 291 (2019) 62-70].

Cegla J, Neely RDG, France M, Ferns G, Byrne CD, Halcox J, Datta D, Capps N, Shoulders C, Qureshi N, Rees A, Main L, Cramb R, Viljoen A, Payne J, Soran H; HEART UK Medical, Scientific and Research Committee. Cegla J, et al. Atherosclerosis. 2020 Mar;296:48. doi: 10.1016/j.atherosclerosis.2020.01.019. Epub 2020 Feb 1. Atherosclerosis. 2020. PMID: 32018073 No abstract available.

7

Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia.

Narcisi TM, Shoulders CC, Chester SA, Read J, Brett DJ, Harrison GB, Grantham TT, Fox MF, Povey S, de Bruin TW, et al. Narcisi TM, et al. Among authors: shoulders cc. Am J Hum Genet. 1995 Dec;57(6):1298-310. Am J Hum Genet. 1995. PMID: 8533758 Free PMC article.

8

Variation at the apo AI/CIII/AIV gene complex is associated with elevated plasma levels of apo CIII.

Shoulders CC, Harry PJ, Lagrost L, White SE, Shah NF, North JD, Gilligan M, Gambert P, Ball MJ. Shoulders CC, et al. Atherosclerosis. 1991 Apr;87(2-3):239-47. doi: 10.1016/0021-9150(91)90026-y. Atherosclerosis. 1991. PMID: 1906714

9

Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein.

Shoulders CC, Brett DJ, Bayliss JD, Narcisi TM, Jarmuz A, Grantham TT, Leoni PR, Bhattacharya S, Pease RJ, Cullen PM, et al. Shoulders CC, et al. Hum Mol Genet. 1993 Dec;2(12):2109-16. doi: 10.1093/hmg/2.12.2109. Hum Mol Genet. 1993. PMID: 8111381

10

Characterization of genetic markers in the 5'flanking region of the apo A1 gene.

Shoulders CC, Narcisi TM, Jarmuz A, Brett DJ, Bayliss JD, Scott J. Shoulders CC, et al. Hum Genet. 1993 Mar;91(2):197-8. doi: 10.1007/BF00222727. Hum Genet. 1993. PMID: 8096496

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