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Current Protocols in Human Genetics|January 12, 2010
Acylcarnitine analysis by tandem mass spectrometryEmily H Smith, Dietrich MaternActa Paediatrica (Oslo, Norway : 1992)|May 28, 2008
Newborn screening for lysosomal storage disordersDietrich MaternMolecular Genetics and Metabolism|May 4, 2010
Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencingEmily H Smith, Cheryl Thomas, David McHugh, et al.Developmental Disabilities Research Reviews|June 26, 2013
Newborn screening for lysosomal storage disorders and other neuronopathic conditionsDietrich Matern, Devin Oglesbee, Silvia TortorelliCurrent Opinion in Pediatrics|July 27, 2004
Recent developments and new applications of tandem mass spectrometry in newborn screeningPiero Rinaldo, Silvia Tortorelli, Dietrich MaternMolecular Genetics and Metabolism|May 18, 2005
In vitro correction of medium chain acyl CoA dehydrogenase deficiency with a recombinant adenoviral vectorDavid B Schowalter, Dietrich Matern, Jerry VockleyGenetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2008
Acylcarnitine profile analysisPiero Rinaldo, Tina M Cowan, Dietrich MaternJournal of Inherited Metabolic Disease|April 8, 2010
Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meetingMartin Lindner, Georg F Hoffmann, Dietrich MaternAnnual Review of Physiology|February 5, 2002
Fatty acid oxidation disordersPiero Rinaldo, Dietrich Matern, Michael J BennettTopics in Clinical Nutrition|July 1, 2010
EFFECT OF FEEDING, EXERCISE AND GENOTYPE ON PLASMA 3-HYDROXYACYLCARNITINES IN CHILDREN WITH LCHAD DEFICIENCYMelanie B Gillingham, Dietrich Matern, Cary O HardingPageof 17