Wiley V - Search Results

1

Maternal attitudes to newborn screening for fragile X syndrome.

Christie L, Wotton T, Bennetts B, Wiley V, Wilcken B, Rogers C, Boyle J, Turner C, Hansen J, Hunter M, Goel H, Field M. Christie L, et al. Among authors: wiley v. Am J Med Genet A. 2013 Feb;161A(2):301-11. doi: 10.1002/ajmg.a.35752. Epub 2013 Jan 9. Am J Med Genet A. 2013. PMID: 23303663

2

Neonatal screening for cystic fibrosis: a comparison of two strategies for case detection in 1.2 million babies.

Wilcken B, Wiley V, Sherry G, Bayliss U. Wilcken B, et al. Among authors: wiley v. J Pediatr. 1995 Dec;127(6):965-70. doi: 10.1016/s0022-3476(95)70040-4. J Pediatr. 1995. PMID: 8523199

3

Newborn screening for congenital adrenal hyperplasia: testing to commence in New South Wales.

Wilcken B, Wiley V. Wilcken B, et al. Among authors: wiley v. J Paediatr Child Health. 1996 Feb;32(1):76. J Paediatr Child Health. 1996. PMID: 8652225 No abstract available.

4

Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia.

Wiley V, Carpenter K, Wilcken B. Wiley V, et al. Acta Paediatr Suppl. 1999 Dec;88(432):48-51. doi: 10.1111/j.1651-2227.1999.tb01157.x. Acta Paediatr Suppl. 1999. PMID: 10626578

5

Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile.

Sim KG, Wiley V, Carpenter K, Wilcken B. Sim KG, et al. Among authors: wiley v. J Inherit Metab Dis. 2001 Feb;24(1):51-9. doi: 10.1023/a:1005606805951. J Inherit Metab Dis. 2001. PMID: 11286383

6

Carnitine transporter defect diagnosed by newborn screening with electrospray tandem mass spectrometry.

Wilcken B, Wiley V, Sim KG, Carpenter K. Wilcken B, et al. Among authors: wiley v. J Pediatr. 2001 Apr;138(4):581-4. doi: 10.1067/mpd.2001.111813. J Pediatr. 2001. PMID: 11295726

7

Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies.

Carpenter K, Wiley V, Sim KG, Heath D, Wilcken B. Carpenter K, et al. Among authors: wiley v. Arch Dis Child Fetal Neonatal Ed. 2001 Sep;85(2):F105-9. doi: 10.1136/fn.85.2.f105. Arch Dis Child Fetal Neonatal Ed. 2001. PMID: 11517203 Free PMC article.

8

Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency.

Wilcken B, Carpenter K, Wiley V. Wilcken B, et al. Among authors: wiley v. Lancet. 2002 Feb 16;359(9306):627-8. doi: 10.1016/S0140-6736(02)07730-9. Lancet. 2002. PMID: 11867142 No abstract available.

9

Neonatal thyroid-stimulating hormone concentrations in northern Sydney: further indications of mild iodine deficiency?

McElduff A, McElduff P, Gunton JE, Hams G, Wiley V, Wilcken BM. McElduff A, et al. Among authors: wiley v. Med J Aust. 2002 Apr 1;176(7):317-20. doi: 10.5694/j.1326-5377.2002.tb04431.x. Med J Aust. 2002. PMID: 12013323

10

Screening newborns for inborn errors of metabolism by tandem mass spectrometry.

Wilcken B, Wiley V, Hammond J, Carpenter K. Wilcken B, et al. Among authors: wiley v. N Engl J Med. 2003 Jun 5;348(23):2304-12. doi: 10.1056/NEJMoa025225. N Engl J Med. 2003. PMID: 12788994 Free article.

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