McDowell I - Search Results

1

Estimation of the prevalence of cholesteryl ester storage disorder in a cohort of patients with clinical features of familial hypercholesterolaemia.

Ashfield-Watt P, Haralambos K, Edwards R, Townsend D, Gingell R, Wa Li K, Humphries SE, McDowell I. Ashfield-Watt P, et al. Among authors: mcdowell i. Ann Clin Biochem. 2019 Jan;56(1):112-117. doi: 10.1177/0004563218793165. Epub 2018 Aug 8. Ann Clin Biochem. 2019. PMID: 30056760

2

Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales.

Haralambos K, Whatley SD, Edwards R, Gingell R, Townsend D, Ashfield-Watt P, Lansberg P, Datta DB, McDowell IF. Haralambos K, et al. Among authors: mcdowell if. Atherosclerosis. 2015 May;240(1):190-6. doi: 10.1016/j.atherosclerosis.2015.03.003. Epub 2015 Mar 6. Atherosclerosis. 2015. PMID: 25797312

3

Diagnostic scoring for familial hypercholesterolaemia in practice.

Haralambos K, Ashfield-Watt P, McDowell IF. Haralambos K, et al. Curr Opin Lipidol. 2016 Aug;27(4):367-74. doi: 10.1097/MOL.0000000000000325. Curr Opin Lipidol. 2016. PMID: 27389632 Review.

4

Non-HDL or LDL cholesterol in heterozygous familial hypercholesterolaemia: findings of the Simon Broome Register.

Soran H, Cooper JA, Durrington PN, Capps N, McDowell IFW, Humphries SE, Neil A; Simon Broome Familial Hyperlipidaemia Register Group. Soran H, et al. Curr Opin Lipidol. 2020 Aug;31(4):167-175. doi: 10.1097/MOL.0000000000000692. Curr Opin Lipidol. 2020. PMID: 32618729 Review.

5

Sex differences in cardiovascular morbidity associated with familial hypercholesterolaemia: A retrospective cohort study of the UK Simon Broome register linked to national hospital records.

Iyen B, Qureshi N, Weng S, Roderick P, Kai J, Capps N, Durrington PN, McDowell IF, Soran H, Neil A, Humphries SE. Iyen B, et al. Atherosclerosis. 2020 Dec;315:131-137. doi: 10.1016/j.atherosclerosis.2020.10.895. Epub 2020 Oct 31. Atherosclerosis. 2020. PMID: 33187671 Free PMC article.

6

Coronary heart disease mortality in severe vs. non-severe familial hypercholesterolaemia in the Simon Broome Register.

Humphries SE, Cooper JA, Capps N, Durrington PN, Jones B, McDowell IFW, Soran H, Neil AHW; Simon Broome Familial Hyperlipidaemia Register Group. Humphries SE, et al. Atherosclerosis. 2019 Feb;281:207-212. doi: 10.1016/j.atherosclerosis.2018.11.014. Epub 2018 Nov 12. Atherosclerosis. 2019. PMID: 30458964 Free PMC article.

7

Coronary heart disease mortality in treated familial hypercholesterolaemia: Update of the UK Simon Broome FH register.

Humphries SE, Cooper JA, Seed M, Capps N, Durrington PN, Jones B, McDowell IFW, Soran H, Neil HAW; Simon Broome Familial Hyperlipidaemia Register Group. Humphries SE, et al. Among authors: mcdowell ifw. Atherosclerosis. 2018 Jul;274:41-46. doi: 10.1016/j.atherosclerosis.2018.04.040. Epub 2018 May 1. Atherosclerosis. 2018. PMID: 29751283 Free PMC article.

8

Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study.

Neil A, Cooper J, Betteridge J, Capps N, McDowell I, Durrington P, Seed M, Humphries SE. Neil A, et al. Among authors: mcdowell i. Eur Heart J. 2008 Nov;29(21):2625-33. doi: 10.1093/eurheartj/ehn422. Epub 2008 Oct 7. Eur Heart J. 2008. PMID: 18840879 Free PMC article.

9

Effect of riboflavin status on the homocysteine-lowering effect of folate in relation to the MTHFR (C677T) genotype.

Moat SJ, Ashfield-Watt PA, Powers HJ, Newcombe RG, McDowell IF. Moat SJ, et al. Clin Chem. 2003 Feb;49(2):295-302. doi: 10.1373/49.2.295. Clin Chem. 2003. PMID: 12560354 Clinical Trial.

10

Methylenetetrahydrofolate reductase 677C-->T genotype modulates homocysteine responses to a folate-rich diet or a low-dose folic acid supplement: a randomized controlled trial.

Ashfield-Watt PA, Pullin CH, Whiting JM, Clark ZE, Moat SJ, Newcombe RG, Burr ML, Lewis MJ, Powers HJ, McDowell IF. Ashfield-Watt PA, et al. Am J Clin Nutr. 2002 Jul;76(1):180-6. doi: 10.1093/ajcn/76.1.180. Am J Clin Nutr. 2002. PMID: 12081832 Clinical Trial.

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