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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Disorders of fatty acid transport and mitochondrial oxidation: challenges and dilemmas of metabolic evaluationP Rinaldo, D MaternThe Journal of Nutrition|May 8, 2001
Mass spectrometry methods for metabolic and health assessmentD Matern, M J MageraHuman Mutation|December 29, 1999
Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutationsH H Seydewitz, D MaternActa Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
Clinical biochemical genetics in the twenty-first centuryP Rinaldo, S Hahn, D MaternAnnals of Biomedical Engineering|February 21, 2002
Quantitative measurements of the mechanical properties of human bone tissues by scanning acoustic microscopyI Eckardt, H J HeinEuropean Journal of Pediatrics|January 1, 1993
Purification of human microsomal liver glucose-6-phosphatase system by affinity chromatography and immunodetectionS Kösel, D Matern, Y S ShinJournal of Inherited Metabolic Disease|January 1, 1996
Seizures in a boy with succinic semialdehyde dehydrogenase deficiency treated with vigabatrin (gamma-vinyl-GABA)D Matern, W Lehnert, K M Gibson, et al.Klinische Padiatrie|November 26, 1999
[Atypical course of a multiple acyl-CoA-dehydrogenase deficiency]M Rose, D Matern, D S Millington, et al.European Journal of Pediatrics|August 1, 1996
Dyslipidaemia in a boy with recurrent abdominal pain, hypersalivation and decreased lipoprotein lipase activityD Matern, H Seydewitz, H Niederhoff, et al.Journal of Inherited Metabolic Disease|July 24, 2007
Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007)D Matern, S Tortorelli, D Oglesbee, et al.Pageof 4