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Items: 1 to 20 of 190

1.

National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.

Dietzen DJ, Rinaldo P, Whitley RJ, Rhead WJ, Hannon WH, Garg UC, Lo SF, Bennett MJ.

Clin Chem. 2009 Sep;55(9):1615-26. doi: 10.1373/clinchem.2009.131300. Epub 2009 Jul 2.

2.
3.

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

Simonsen H.

Ugeskr Laeger. 2002 Nov 25;164(48):5607-12. Review. Danish.

PMID:
12523003
4.

A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing.

Chace DH, Kalas TA.

Clin Biochem. 2005 Apr;38(4):296-309. Review. Erratum in: Clin Biochem. 2005 May;38(5):495.

PMID:
15766731
5.

Newborn screening for inborn errors of metabolism: a systematic review.

Seymour CA, Thomason MJ, Chalmers RA, Addison GM, Bain MD, Cockburn F, Littlejohns P, Lord J, Wilcox AH.

Health Technol Assess. 1997;1(11):i-iv, 1-95. Review.

6.

Newborn screening.

Wilcken B, Wiley V.

Pathology. 2008 Feb;40(2):104-15. doi: 10.1080/00313020701813743. Review.

PMID:
18203033
7.

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism.

Thomason MJ, Lord J, Bain MD, Chalmers RA, Littlejohns P, Addison GM, Wilcox AH, Seymour CA.

J Public Health Med. 1998 Sep;20(3):331-43. Review.

PMID:
9793900
8.

Newborn screening: an overview.

Carreiro-Lewandowski E.

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

PMID:
12776783
9.

The call from the newborn screening laboratory: frustration in the afternoon.

Rhead WJ, Irons M.

Pediatr Clin North Am. 2004 Jun;51(3):803-18, xii. Review.

PMID:
15157599
10.

[Neonatal screening by tandem mass spectrometry: an update].

Campos Hernández D.

Rev Panam Salud Publica. 2010 Apr;27(4):309-17. Review. Spanish.

11.

Expanded newborn screening of inherited metabolic disorders by tandem mass spectrometry: clinical and laboratory aspects.

Garg U, Dasouki M.

Clin Biochem. 2006 Apr;39(4):315-32. Epub 2006 Mar 23. Review.

PMID:
16563365
12.

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
13.

[Tandem mass spectrometry as screening for inborn errors of metabolism].

Campos H D.

Rev Med Chil. 2011 Oct;139(10):1356-64. doi: /S0034-98872011001000017. Epub 2012 Jan 3. Review. Spanish.

14.

Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns.

Chace DH, Kalas TA, Naylor EW.

Clin Chem. 2003 Nov;49(11):1797-817. Review.

15.

Tandem mass spectrometry newborn screening for inborn errors of intermediary metabolism: abnormal profile interpretation.

Fernández-Lainez C, Aguilar-Lemus JJ, Vela-Amieva M, Ibarra-González I.

Curr Med Chem. 2012;19(26):4511-22. Review.

PMID:
22934775
16.
17.

A review of newborn screening in the era of tandem mass spectrometry: what's new for the pediatric neurologist?

Copeland S.

Semin Pediatr Neurol. 2008 Sep;15(3):110-6. doi: 10.1016/j.spen.2008.05.003. Review.

PMID:
18708000
18.

Newborn screening: current status.

Arn PH.

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

PMID:
17339686
19.

Expanded newborn screening and confirmatory follow-up testing for inborn errors of metabolism detected by tandem mass spectrometry.

Ozben T.

Clin Chem Lab Med. 2013 Jan;51(1):157-76. doi: 10.1515/cclm-2012-0472. Review.

PMID:
23183752
20.

Current approaches to genetic metabolic screening in newborns.

Levy HL, Cornier AS.

Curr Opin Pediatr. 1994 Dec;6(6):707-11. Review.

PMID:
7849819

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