Dietrich Matern
Biochemical Genetics Laboratory
Division of Laboratory Genetics
Department of Laboratory Medicine and Pathology
Mayo Clinic
USA
Name/email consistency: high
- Newborn screening for lysosomal storage disorders. Matern, D. Acta. Paediatr. Suppl (2008)
- Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007). Matern, D., Tortorelli, S., Oglesbee, D., Gavrilov, D., Rinaldo, P. J. Inherit. Metab. Dis. (2007)
- Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry. Matern, D., He, M., Berry, S.A., Rinaldo, P., Whitley, C.B., Madsen, P.P., van Calcar, S.C., Lussky, R.C., Andresen, B.S., Wolff, J.A., Vockley, J. Pediatrics (2003)
- Glycogen storage disease type I: diagnosis and phenotype/genotype correlation. Matern, D., Seydewitz, H.H., Bali, D., Lang, C., Chen, Y.T. Eur. J. Pediatr. (2002)
- Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency. Matern, D., Schehata, B.M., Shekhawa, P., Strauss, A.W., Bennett, M.J., Rinaldo, P. Mol. Genet. Metab. (2001)
- Mass spectrometry methods for metabolic and health assessment. Matern, D., Magera, M.J. J. Nutr. (2001)
