Taylor A - Search Results

1

Polymorphous lymphoproliferative disorder with Hodgkin-like features in common γ-chain-deficient severe combined immunodeficiency.

Slatter MA, Angus B, Windebank K, Taylor A, Meaney C, Lester T, Norbury G, Hambleton S, Abinun M, Flood TJ, Cant AJ, Gennery AR. Slatter MA, et al. Among authors: taylor a. J Allergy Clin Immunol. 2011 Feb;127(2):533-5. doi: 10.1016/j.jaci.2010.09.036. Epub 2010 Nov 20. J Allergy Clin Immunol. 2011. PMID: 21094519 No abstract available.

2

Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia.

Taylor A, Martin B, Wang D, Patel K, Humphries SE, Norbury G. Taylor A, et al. Clin Genet. 2009 Jul;76(1):69-75. doi: 10.1111/j.1399-0004.2009.01168.x. Epub 2009 Jun 16. Clin Genet. 2009. PMID: 19538517

3

Mutation screening in patients for familial hypercholesterolaemia (ADH).

Taylor A, Patel K, Tsedeke J, Humphries SE, Norbury G. Taylor A, et al. Clin Genet. 2010 Jan;77(1):97-9. doi: 10.1111/j.1399-0004.2009.01279.x. Epub 2009 Oct 14. Clin Genet. 2010. PMID: 19843101 No abstract available.

4

A double heterozygote for familial hypercholesterolaemia and familial defective apolipoprotein B-100.

Taylor A, Bayly G, Patel K, Yarram L, Williams M, Hamilton-Shield J, Humphries SE, Norbury G. Taylor A, et al. Ann Clin Biochem. 2010 Sep;47(Pt 5):487-90. doi: 10.1258/acb.2010.010089. Epub 2010 Aug 24. Ann Clin Biochem. 2010. PMID: 20736250

5

A functional mutation in the LDLR promoter (-139C>G) in a patient with familial hypercholesterolemia.

Smith AJ, Ahmed F, Nair D, Whittall R, Wang D, Taylor A, Norbury G, Humphries SE. Smith AJ, et al. Among authors: taylor a. Eur J Hum Genet. 2007 Nov;15(11):1186-9. doi: 10.1038/sj.ejhg.5201897. Epub 2007 Jul 11. Eur J Hum Genet. 2007. PMID: 17625505

6

Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia.

Taylor A, Tabrah S, Wang D, Sozen M, Duxbury N, Whittall R, Humphries SE, Norbury G. Taylor A, et al. Clin Genet. 2007 Jun;71(6):561-8. doi: 10.1111/j.1399-0004.2007.00807.x. Clin Genet. 2007. PMID: 17539906

7

Homozygous hypercholesterolaemia and ezetimibe: a case report.

Hendriksz CJ, Norbury G, Tabrah S, Taylor A, Humphries SE. Hendriksz CJ, et al. Among authors: taylor a. Acta Paediatr. 2004 Feb;93(2):280-2. Acta Paediatr. 2004. PMID: 15046291

8

Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project.

Taylor A, Wang D, Patel K, Whittall R, Wood G, Farrer M, Neely RD, Fairgrieve S, Nair D, Barbir M, Jones JL, Egan S, Everdale R, Lolin Y, Hughes E, Cooper JA, Hadfield SG, Norbury G, Humphries SE. Taylor A, et al. Clin Genet. 2010 Jun;77(6):572-80. doi: 10.1111/j.1399-0004.2009.01356.x. Epub 2010 Mar 13. Clin Genet. 2010. PMID: 20236128

9

Barcoded Hybrids of Extracellular Vesicles and Lipid Nanoparticles for Multiplexed Analysis of Tissue Distribution.

Ivanova A, Chalupska R, Louro AF, Firth M, González-King Garibotti H, Hultin L, Kohl F, Lázaro-Ibáñez E, Lindgren J, Musa G, Oude Blenke E, Silva AM, Szeponik L, Taylor A, Viken I, Wang X, Jennbacken K, Wiseman J, Dekker N. Ivanova A, et al. Among authors: taylor a. Adv Sci (Weinh). 2025 Jan 16:e2407850. doi: 10.1002/advs.202407850. Online ahead of print. Adv Sci (Weinh). 2025. PMID: 39823165

10

Child-report food insecurity assessment measures: a scoping review.

Taylor AJ, Baker S, Gallegos D. Taylor AJ, et al. Appetite. 2025 Jan 13:107854. doi: 10.1016/j.appet.2025.107854. Online ahead of print. Appetite. 2025. PMID: 39814201 Review.

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