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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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 11, 2013
Multiplex newborn screening for Pompe, Fabry, Hunter, Gaucher, and Hurler diseases using a digital microfluidic platformRamakrishna S Sista, Tong Wang, Ning Wu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 2012
An improved method for glycosaminoglycan analysis by LC-MS/MS of urine samples collected on filter paperChristiane Auray-Blais, Pamela Lavoie, Haoyue Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2006
Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe diseaseHaoyue Zhang, Helmut Kallwass, Sarah P Young, et al.
Molecular Genetics and Metabolism|January 10, 2012
A novel fluorometric enzyme analysis method for Hunter syndrome using dried blood spotsAdviye A Tolun, Carrie Graham, Qun Shi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 23, 2020
Comparison of dermatan sulfate and heparan sulfate concentrations in serum, cerebrospinal fluid and urine in patients with mucopolysaccharidosis type I receiving intravenous and intrathecal enzyme replacement therapyHaoyue Zhang, Patricia I Dickson, Ashlee R Stiles, et al.
Annals of Epidemiology|October 16, 2012
Systemic oxidative stress, as measured by urinary allantoin and F(2)-isoprostanes, is not increased in Down syndromeAdviye A Tolun, Peter M Scarbrough, Haoyue Zhang, et al.
Journal of Neurochemistry|February 6, 2008
Brain-specific carnitine palmitoyl-transferase-1c: role in CNS fatty acid metabolism, food intake, and body weightMichael J Wolfgang, Seung Hun Cha, David S Millington, et al.
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