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Newborn Screening for Lysosomal Storage Disorders: Quo Vadis?
Peake RW, Marsden DL, Bodamer OA, Gelb MH, Millington DS, Wijburg F. Peake RW, et al. Clin Chem. 2016 Nov;62(11):1430-1438. doi: 10.1373/clinchem.2016.258459. Epub 2016 Sep 14. Clin Chem. 2016. PMID: 27630153 Free PMC article. No abstract available.
Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening.
Hsu HW, Zytkovicz TH, Comeau AM, Strauss AW, Marsden D, Shih VE, Grady GF, Eaton RB. Hsu HW, et al. Pediatrics. 2008 May;121(5):e1108-14. doi: 10.1542/peds.2007-1993. Pediatrics. 2008. PMID: 18450854
Newborn screening for metabolic disorders.
Marsden D, Larson C, Levy HL. Marsden D, et al. J Pediatr. 2006 May;148(5):577-584. doi: 10.1016/j.jpeds.2005.12.021. J Pediatr. 2006. PMID: 16737864 Review. No abstract available.
Newborn screening of lysosomal storage disorders.
Marsden D, Levy H. Marsden D, et al. Clin Chem. 2010 Jul;56(7):1071-9. doi: 10.1373/clinchem.2009.141622. Epub 2010 May 20. Clin Chem. 2010. PMID: 20489136 Review.
Newborn screening.
Sahai I, Marsden D. Sahai I, et al. Crit Rev Clin Lab Sci. 2009;46(2):55-82. doi: 10.1080/10408360802485305. Crit Rev Clin Lab Sci. 2009. PMID: 19255915 Review.
Expanded newborn screening.
Fearing MK, Marsden D. Fearing MK, et al. Pediatr Ann. 2003 Aug;32(8):509-15. doi: 10.3928/0090-4481-20030801-08. Pediatr Ann. 2003. PMID: 12942893
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