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Molecular Genetics and Metabolism|May 12, 2005
Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe diseaseYan An, Sarah P Young, Priya S Kishnani, et al.
Bio Systems|March 13, 2002
Robustness of MetaNet graph models: predicting control of urea production in humansMichael C Kohn, Abdul S Tohmaz, Karen J Giroux, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2009
Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarkerSarah P Young, Haoyue Zhang, Deyanira Corzo, et al.
Clinical Biochemistry|September 17, 2013
Novel application of digital microfluidics for the detection of biotinidase deficiency in newbornsCarrie Graham, Ramakrishna S Sista, Jairus Kleinert, et al.
Molecular Genetics and Metabolism|April 13, 2013
Rapid assays for Gaucher and Hurler diseases in dried blood spots using digital microfluidicsRamakrishna S Sista, Tong Wang, Ning Wu, et al.
Seminars in Perinatology|March 9, 2010
Digital microfluidics: a future technology in the newborn screening laboratory?David S Millington, Ramakrishna Sista, Allen Eckhardt, et al.
Journal of the American Society for Mass Spectrometry|May 24, 2021
Capillary Electrophoresis-High Resolution Mass Spectrometry for Measuring In Vivo Arginine Isotope Incorporation in Alzheimer's Disease Mouse ModelsKendra J Adams, Joan G Wilson, David S Millington, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 22, 2003
A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiencySarah P Young, Dietrich Matern, Niels Gregersen, et al.
Diabetes Care|November 22, 2011
Urinary F2-isoprostanes as a biomarker of reduced risk of type 2 diabetesDora Il'yasova, Ivan Spasojevic, Karel Base, et al.
Molecular Genetics and Metabolism|October 12, 2010
Efficient analysis of urinary glycosaminoglycans by LC-MS/MS in mucopolysaccharidoses type I, II and VIChristiane Auray-Blais, Patrick Bhérer, René Gagnon, et al.
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