Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases

Author:

Ramsay Steven L.,Maire Irene,Bindloss Colleen,Fuller Maria,Whitfield Phillip D.,Piraud Monique,Hopwood John J.,Meikle Peter J.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference22 articles.

1. Lysosomal disorders;Wraith;Semin. Neonatol.,2002

2. Diagnosis of lysosomal storage disorders: evaluation of lysosome-associated membrane protein LAMP-1 as a diagnostic marker;Meikle;Clin. Chem.,1997

3. Saposins A, B, C, and D in plasma of patients with lysosomal storage disorders;Chang;Clin. Chem.,2000

4. J.E. Robillard, C.C. Porter, P.A. Jose, Structure and function of the developing kidney, Chapter 2, in: M.A. Holliday, T.M. Barratt, E.D. Avner, (Eds.), Pediatric Nephrology, third ed., Williams and Wilkins, Baltimore, 1994, p. 26

5. Prenatal diagnosis of lysosomal storage diseases;Lake;Brain Pathol.,1998

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