Naylor EW - Search Results

1

Twenty-year follow-up of newborn screening for patients with muscular dystrophy.

Chung J, Smith AL, Hughes SC, Niizawa G, Abdel-Hamid HZ, Naylor EW, Hughes T, Clemens PR. Chung J, et al. Among authors: naylor ew. Muscle Nerve. 2016 Apr;53(4):570-8. doi: 10.1002/mus.24880. Epub 2015 Sep 10. Muscle Nerve. 2016. PMID: 26260293

2

Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy.

Wood MF, Hughes SC, Hache LP, Naylor EW, Abdel-Hamid HZ, Barmada MM, Dobrowolski SF, Stickler DE, Clemens PR. Wood MF, et al. Among authors: naylor ew. Muscle Nerve. 2014 Jun;49(6):822-8. doi: 10.1002/mus.24100. Muscle Nerve. 2014. PMID: 24307279

3

Newborn screening for spinal muscular atrophy by calibrated short-amplicon melt profiling.

Dobrowolski SF, Pham HT, Downes FP, Prior TW, Naylor EW, Swoboda KJ. Dobrowolski SF, et al. Among authors: naylor ew. Clin Chem. 2012 Jun;58(6):1033-9. doi: 10.1373/clinchem.2012.183038. Epub 2012 Apr 9. Clin Chem. 2012. PMID: 22490618 Free PMC article.

4

Maternal screening for hypothyroidism and thyroiditis using filter paper specimens.

Foley TP Jr, Henry JJ, Hofman LF, Thomas RD, Sanfilippo JS, Naylor EW. Foley TP Jr, et al. Among authors: naylor ew. J Womens Health (Larchmt). 2013 Nov;22(11):991-6. doi: 10.1089/jwh.2013.4393. Epub 2013 Sep 11. J Womens Health (Larchmt). 2013. PMID: 24025107 Free PMC article.

5

A rapid screening test for Duchenne muscular dystrophy using dried blood specimens.

Orfanos AP, Naylor EW. Orfanos AP, et al. Among authors: naylor ew. Clin Chim Acta. 1984 Apr 27;138(3):267-74. doi: 10.1016/0009-8981(84)90133-5. Clin Chim Acta. 1984. PMID: 6723063

6

Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies.

Ziadeh R, Hoffman EP, Finegold DN, Hoop RC, Brackett JC, Strauss AW, Naylor EW. Ziadeh R, et al. Among authors: naylor ew. Pediatr Res. 1995 May;37(5):675-8. doi: 10.1203/00006450-199505000-00021. Pediatr Res. 1995. PMID: 7603790

7

Development of DNA confirmatory and high-risk diagnostic testing for newborns using targeted next-generation DNA sequencing.

Bhattacharjee A, Sokolsky T, Wyman SK, Reese MG, Puffenberger E, Strauss K, Morton H, Parad RB, Naylor EW. Bhattacharjee A, et al. Among authors: naylor ew. Genet Med. 2015 May;17(5):337-47. doi: 10.1038/gim.2014.117. Epub 2014 Sep 25. Genet Med. 2015. PMID: 25255367 Free article.

8

New technologies in newborn screening.

Naylor EW. Naylor EW. Yale J Biol Med. 1991 Jan-Feb;64(1):21-4. Yale J Biol Med. 1991. PMID: 1897257 Free PMC article. No abstract available.

9

Real time PCR assays to detect common mutations in the biotinidase gene and application of mutational analysis to newborn screening for biotinidase deficiency.

Dobrowolski SF, Angeletti J, Banas RA, Naylor EW. Dobrowolski SF, et al. Among authors: naylor ew. Mol Genet Metab. 2003 Feb;78(2):100-7. doi: 10.1016/s1096-7192(02)00231-7. Mol Genet Metab. 2003. PMID: 12618081

10

DNA microarray technology for neonatal screening.

Dobrowolski SF, Banas RA, Naylor EW, Powdrill T, Thakkar D. Dobrowolski SF, et al. Among authors: naylor ew. Acta Paediatr Suppl. 1999 Dec;88(432):61-4. doi: 10.1111/j.1651-2227.1999.tb01161.x. Acta Paediatr Suppl. 1999. PMID: 10626582

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