Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 30

1.

Newborn screening: toward a uniform screening panel and system.

[No authors listed]

Genet Med. 2006 May;8 Suppl 1:1S-252S.

2.

An overview of newborn screening.

Levy PA.

J Dev Behav Pediatr. 2010 Sep;31(7):622-31. doi: 10.1097/DBP.0b013e3181eedf01. Review.

PMID:
20814260
3.

Navigating the maze of newborn screening.

Spahis JK, Bowers NR.

MCN Am J Matern Child Nurs. 2006 May-Jun;31(3):190-6. Review.

PMID:
16679962
4.

Policy issues related to expanded newborn screening: a review of three genetic/metabolic disorders.

Bishop Hubbard H.

Policy Polit Nurs Pract. 2007 Aug;8(3):201-9. doi: 10.1177/1527154407303498. Review.

PMID:
18178927
5.

Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.

Bailey DB Jr, Skinner D, Davis AM, Whitmarsh I, Powell C.

Pediatrics. 2008 Mar;121(3):e693-704. doi: 10.1542/peds.2007-0820. Review.

PMID:
18310190
6.

A primer on economic evaluations related to expansion of newborn screening for genetic and metabolic disorders.

Hubbard HB.

J Obstet Gynecol Neonatal Nurs. 2006 Nov-Dec;35(6):692-9. Review.

PMID:
17105633
7.

Newborn screening: an overview.

Carreiro-Lewandowski E.

Clin Lab Sci. 2002 Fall;15(4):229-38. Review.

PMID:
12776783
8.

Newborn genetic screening: blessing or curse?

Kenner C, Amlung S.

Neonatal Netw. 1999 Oct;18(7):11-9. Review.

PMID:
10808884
9.

Newborn screening: current status.

Arn PH.

Health Aff (Millwood). 2007 Mar-Apr;26(2):559-66. Review.

PMID:
17339686
10.

Neonatal genetic testing is more than screening.

Kenner C, Lewis JA, Pressler JL, Little CM.

Crit Care Nurs Clin North Am. 2008 Jun;20(2):233-7, vii. doi: 10.1016/j.ccell.2008.01.005. Review.

PMID:
18424352
11.

Newborn screening for cystic fibrosis.

Rock MJ.

Clin Chest Med. 2007 Jun;28(2):297-305. Review.

PMID:
17467549
12.

[Mass neonatal screening using biological testing].

Ardaillou R, Le Gall JY; Commission I (Annexe A) de l'Académie Nationale de Médecine.

Gynecol Obstet Fertil. 2007 Apr;35(4):367-74. Epub 2007 Apr 2. French.

PMID:
17400505
13.

U.S. newborn screening policy dilemmas for the twenty-first century.

Therrell BL Jr.

Mol Genet Metab. 2001 Sep-Oct;74(1-2):64-74. Review.

PMID:
11592804
14.

Cost-effectiveness and test-performance factors in relation to universal newborn hearing screening.

Gorga MP, Neely ST.

Ment Retard Dev Disabil Res Rev. 2003;9(2):103-8. Review.

PMID:
12784228
15.

Phenylketonuria (PKU): screening and management.

[No authors listed]

NIH Consens Statement. 2000 Oct 16-18;17(3):1-33. Review.

PMID:
11757784
16.

Current status of newborn screening: decision-making about the conditions to include in screening programs.

Watson MS.

Ment Retard Dev Disabil Res Rev. 2006;12(4):230-5. Review.

PMID:
17183572
17.

State-of-the-art for DNA technology in newborn screening.

McCabe ER, McCabe LL.

Acta Paediatr Suppl. 1999 Dec;88(432):58-60. Review.

PMID:
10626581
18.

Understanding newborn screening system issues with emphasis on cystic fibrosis screening.

Therrell BL, Lloyd-Puryear MA, Mann MY.

J Pediatr. 2005 Sep;147(3 Suppl):S6-10. Review.

PMID:
16202785
19.

Newborn screening and genetic testing.

Kenner C, Moran M.

J Midwifery Womens Health. 2005 May-Jun;50(3):219-26. Review.

PMID:
15895000
20.

Newborn genetic screening.

Wallman CM.

Neonatal Netw. 1998 Apr;17(3):55-60. Review. No abstract available.

PMID:
9601352

Supplemental Content

Support Center