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Page 1
A Prospective Study of Sudden Cardiac Death among Children and Young Adults.
Bagnall RD, Weintraub RG, Ingles J, Duflou J, Yeates L, Lam L, Davis AM, Thompson T, Connell V, Wallace J, Naylor C, Crawford J, Love DR, Hallam L, White J, Lawrence C, Lynch M, Morgan N, James P, du Sart D, Puranik R, Langlois N, Vohra J, Winship I, Atherton J, McGaughran J, Skinner JR, Semsarian C. Bagnall RD, et al. Among authors: du sart d. N Engl J Med. 2016 Jun 23;374(25):2441-52. doi: 10.1056/NEJMoa1510687. N Engl J Med. 2016. PMID: 27332903 Free article.
Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH.
Chow E, Lipton L, Lynch E, D'Souza R, Aragona C, Hodgkin L, Brown G, Winship I, Barker M, Buchanan D, Cowie S, Nasioulas S, du Sart D, Young J, Leggett B, Jass J, Macrae F. Chow E, et al. Among authors: du sart d, d souza r. Gastroenterology. 2006 Jul;131(1):30-9. doi: 10.1053/j.gastro.2006.03.046. Gastroenterology. 2006. PMID: 16831587
Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis.
Delatycki MB, Allen KJ, Nisselle AE, Collins V, Metcalfe S, du Sart D, Halliday J, Aitken MA, Macciocca I, Hill V, Wakefield A, Ritchie A, Gason AA, Nicoll AJ, Powell LW, Williamson R. Delatycki MB, et al. Among authors: du sart d. Lancet. 2005 Jul 23-29;366(9482):314-6. doi: 10.1016/S0140-6736(05)63012-7. Lancet. 2005. PMID: 16039334
A comprehensive evaluation of myocardial fibrosis in hypertrophic cardiomyopathy with cardiac magnetic resonance imaging: linking genotype with fibrotic phenotype.
Ellims AH, Iles LM, Ling LH, Chong B, Macciocca I, Slavin GS, Hare JL, Kaye DM, Marasco SF, McLean CA, James PA, du Sart D, Taylor AJ. Ellims AH, et al. Among authors: du sart d. Eur Heart J Cardiovasc Imaging. 2014 Oct;15(10):1108-16. doi: 10.1093/ehjci/jeu077. Epub 2014 May 12. Eur Heart J Cardiovasc Imaging. 2014. PMID: 24819852
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness.
Dahl HH, Saunders K, Kelly TM, Osborn AH, Wilcox S, Cone-Wesson B, Wunderlich JL, Du Sart D, Kamarinos M, Gardner RJ, Dennehy S, Williamson R, Vallance N, Mutton P. Dahl HH, et al. Among authors: du sart d. Med J Aust. 2001 Aug 20;175(4):191-4. doi: 10.5694/j.1326-5377.2001.tb143093.x. Med J Aust. 2001. PMID: 11587277
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests.
Archibald AD, Smith MJ, Burgess T, Scarff KL, Elliott J, Hunt CE, McDonald Z, Barns-Jenkins C, Holt C, Sandoval K, Siva Kumar V, Ward L, Allen EC, Collis SV, Cowie S, Francis D, Delatycki MB, Yiu EM, Massie RJ, Pertile MD, du Sart D, Bruno D, Amor DJ. Archibald AD, et al. Among authors: du sart d. Genet Med. 2018 Apr;20(5):513-523. doi: 10.1038/gim.2017.134. Epub 2017 Oct 26. Genet Med. 2018. PMID: 29261177 Free article.
Population screening and cascade testing for carriers of SMA.
Smith M, Calabro V, Chong B, Gardiner N, Cowie S, du Sart D. Smith M, et al. Among authors: du sart d. Eur J Hum Genet. 2007 Jul;15(7):759-66. doi: 10.1038/sj.ejhg.5201821. Epub 2007 Mar 28. Eur J Hum Genet. 2007. PMID: 17392705
50 results