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Journal Abstract Search

549 related items for PubMed ID: 16600651

  • 1. Newborn screening for lysosomal storage disorders.
    Meikle PJ, Grasby DJ, Dean CJ, Lang DL, Bockmann M, Whittle AM, Fietz MJ, Simonsen H, Fuller M, Brooks DA, Hopwood JJ.
    Mol Genet Metab; 2006 Aug; 88(4):307-14. PubMed ID: 16600651
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  • 2. Screening patients referred to a metabolic clinic for lysosomal storage disorders.
    Fuller M, Tucker JN, Lang DL, Dean CJ, Fietz MJ, Meikle PJ, Hopwood JJ.
    J Med Genet; 2011 Jun; 48(6):422-5. PubMed ID: 21415080
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  • 3. Newborn screening for lysosomal storage disorders: clinical evaluation of a two-tier strategy.
    Meikle PJ, Ranieri E, Simonsen H, Rozaklis T, Ramsay SL, Whitfield PD, Fuller M, Christensen E, Skovby F, Hopwood JJ.
    Pediatrics; 2004 Oct; 114(4):909-16. PubMed ID: 15466084
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  • 4. Newborn screening for lysosomal storage disorders.
    Meikle PJ, Ranieri E, Ravenscroft EM, Hua CT, Brooks DA, Hopwood JJ.
    Southeast Asian J Trop Med Public Health; 1999 Oct; 30 Suppl 2():104-10. PubMed ID: 11400743
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  • 13. Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases.
    Ramsay SL, Maire I, Bindloss C, Fuller M, Whitfield PD, Piraud M, Hopwood JJ, Meikle PJ.
    Mol Genet Metab; 2004 Nov; 83(3):231-8. PubMed ID: 15542394
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  • 16. N-acetylgalactosamine-6-sulfatase protein detection in MPS IVA patient and unaffected control samples.
    Parkinson-Lawrence EJ, Muller VJ, Hopwood JJ, Brooks DA.
    Clin Chim Acta; 2007 Feb; 377(1-2):88-91. PubMed ID: 17027703
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