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Dietrich Matern

Showing results (1-10 of 152) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|May 28, 2008
Newborn screening for lysosomal storage disordersDietrich Matern
Molecular Genetics and Metabolism|August 17, 2010
Systematic ranking of inborn errors of metabolism as targets for gene therapySean E Hofherr, Dietrich Matern
Current Protocols in Human Genetics|January 12, 2010
Acylcarnitine analysis by tandem mass spectrometryEmily H Smith, Dietrich Matern
Clinical Chemistry|November 3, 2022
Identification of Decreased Butyrylcholinesterase in Sudden Infant Death Syndrome Is, at Best, a First Step Toward Preventive ScreeningPatricia L Hall, Dietrich Matern
Developmental Disabilities Research Reviews|June 26, 2013
Newborn screening for lysosomal storage disorders and other neuronopathic conditionsDietrich Matern, Devin Oglesbee, Silvia Tortorelli
Current Opinion in Pediatrics|July 27, 2004
Recent developments and new applications of tandem mass spectrometry in newborn screeningPiero Rinaldo, Silvia Tortorelli, Dietrich Matern
Molecular 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 Vockley
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2008
Acylcarnitine profile analysisPiero Rinaldo, Tina M Cowan, Dietrich Matern
Annual Review of Physiology|February 5, 2002
Fatty acid oxidation disordersPiero Rinaldo, Dietrich Matern, Michael J Bennett
JIMD Reports|June 16, 2026
Re: Pegvaliase Treatment for Adolescents With Phenylketonuria: A Multi-Site StudyPatricia L Hall, Coleman Turgeon, Dietrich Matern
Pageof 16

Showing results (1-10 of 152) with videos related to

Sort By:
Pageof 16
Acta Paediatrica (Oslo, Norway : 1992)|May 28, 2008
Newborn screening for lysosomal storage disordersDietrich Matern
Molecular Genetics and Metabolism|August 17, 2010
Systematic ranking of inborn errors of metabolism as targets for gene therapySean E Hofherr, Dietrich Matern
Current Protocols in Human Genetics|January 12, 2010
Acylcarnitine analysis by tandem mass spectrometryEmily H Smith, Dietrich Matern
Clinical Chemistry|November 3, 2022
Identification of Decreased Butyrylcholinesterase in Sudden Infant Death Syndrome Is, at Best, a First Step Toward Preventive ScreeningPatricia L Hall, Dietrich Matern
Developmental Disabilities Research Reviews|June 26, 2013
Newborn screening for lysosomal storage disorders and other neuronopathic conditionsDietrich Matern, Devin Oglesbee, Silvia Tortorelli
Current Opinion in Pediatrics|July 27, 2004
Recent developments and new applications of tandem mass spectrometry in newborn screeningPiero Rinaldo, Silvia Tortorelli, Dietrich Matern
Molecular 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 Vockley
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2008
Acylcarnitine profile analysisPiero Rinaldo, Tina M Cowan, Dietrich Matern
Annual Review of Physiology|February 5, 2002
Fatty acid oxidation disordersPiero Rinaldo, Dietrich Matern, Michael J Bennett
JIMD Reports|June 16, 2026
Re: Pegvaliase Treatment for Adolescents With Phenylketonuria: A Multi-Site StudyPatricia L Hall, Coleman Turgeon, Dietrich Matern
Pageof 16