Burton H - Search Results

1

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.

Sagoo GS, Butterworth AS, Sanderson S, Shaw-Smith C, Higgins JP, Burton H. Sagoo GS, et al. Among authors: burton h. Genet Med. 2009 Mar;11(3):139-46. doi: 10.1097/GIM.0b013e318194ee8f. Genet Med. 2009. PMID: 19367186 Free article. Review.

2

Array-based comparative genomic hybridization for investigating chromosomal abnormalities in patients with learning disability: systematic review meta-analysis of diagnostic and false-positive yields.

Subramonia-Iyer S, Sanderson S, Sagoo G, Higgins J, Burton H, Zimmern R, Kroese M, Brice P, Shaw-Smith C. Subramonia-Iyer S, et al. Among authors: burton h. Genet Med. 2007 Feb;9(2):74-9. doi: 10.1097/gim.0b013e31803141f2. Genet Med. 2007. PMID: 17304048 Free article.

3

The incidence of inherited metabolic disorders in the West Midlands, UK.

Sanderson S, Green A, Preece MA, Burton H. Sanderson S, et al. Among authors: burton h. Arch Dis Child. 2006 Nov;91(11):896-9. doi: 10.1136/adc.2005.091637. Epub 2006 May 11. Arch Dis Child. 2006. PMID: 16690699 Free PMC article.

4

Review of specialist dietitian services in patients with inherited metabolic disease in the United Kingdom.

Burton H, Sanderson S, Dixon M, Hallam P, White F. Burton H, et al. J Hum Nutr Diet. 2007 Apr;20(2):84-92; quiz 92-4. doi: 10.1111/j.1365-277X.2007.00752.x. J Hum Nutr Diet. 2007. PMID: 17374020

5

Systematic review and meta-analysis to estimate the birth prevalence of five inherited metabolic diseases.

Moorthie S, Cameron L, Sagoo GS, Bonham JR, Burton H. Moorthie S, et al. Among authors: burton h. J Inherit Metab Dis. 2014 Nov;37(6):889-98. doi: 10.1007/s10545-014-9729-0. Epub 2014 Jul 15. J Inherit Metab Dis. 2014. PMID: 25022222 Review.

6

Needs assessment and review of services for people with inherited metabolic disease in the United Kingdom.

Burton H, Sanderson S, Shortland G, Lee P. Burton H, et al. J Inherit Metab Dis. 2006 Oct;29(5):667-76. doi: 10.1007/s10545-006-0374-0. Epub 2006 Aug 5. J Inherit Metab Dis. 2006. PMID: 16972174

7

Systematic review of birth prevalence of neural tube defects in India.

Bhide P, Sagoo GS, Moorthie S, Burton H, Kar A. Bhide P, et al. Among authors: burton h. Birth Defects Res A Clin Mol Teratol. 2013 Jul;97(7):437-43. doi: 10.1002/bdra.23153. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 23873811 Review.

8

Health needs assessment for congenital anomalies in middle-income countries: Examining the case for neural tube defects in Brazil.

Schuler-Faccini L, Sanseverino MT, de Rocha Azevedo LM, Moorthie S, Alberg C, Chowdhury S, Sagoo GS, Burton H, Nacul LC. Schuler-Faccini L, et al. Among authors: burton h. J Community Genet. 2014 Apr;5(2):147-55. doi: 10.1007/s12687-013-0165-x. Epub 2013 Aug 30. J Community Genet. 2014. PMID: 23990401 Free PMC article.

9

Inherited cardiovascular conditions: the challenges of genomic medicine.

Burton H, Alberg C, Hall A, Sagoo GS, Stewart A; Inherited Cardiovascular Conditions Services. Burton H, et al. Heart. 2010 Mar;96(6):474-6. doi: 10.1136/hrt.2009.189159. Heart. 2010. PMID: 20299419

10

Inherited cardiomyopathies.

Raju H, Alberg C, Sagoo GS, Burton H, Behr ER. Raju H, et al. Among authors: burton h. BMJ. 2011 Nov 21;343:d6966. doi: 10.1136/bmj.d6966. BMJ. 2011. PMID: 22106372 Review. No abstract available.

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