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Newborn screening by tandem mass spectrometry for glutaric aciduria type 1: a cost-effectiveness analysis

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Glutaric aciduria type I (GA-I) is a rare metabolic disorder caused by inherited deficiency of glutaryl-CoA dehydrogenase. Despite high prognostic relevance of early diagnosis and start of metabolic treatment as well as an additional cost saving potential later in life, only a limited number of coun...

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Main Authors: Pfeil, Johannes (Author) , Listl, Stefan (Author) , Hoffmann, Georg F. (Author) , Kölker, Stefan (Author) , Lindner, Martin (Author) , Burgard, Peter (Author)
Format: Article (Journal)
Language:English
Published: 17 October 2013
In: Orphanet journal of rare diseases
Year: 2013, Volume: 8, Pages: 1-11
ISSN:1750-1172
DOI:10.1186/1750-1172-8-167
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1186/1750-1172-8-167
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Author Notes:Johannes Pfeil, Stefan Listl, Georg F. Hoffmann, Stefan Kölker, Martin Lindner and Peter Burgard
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Newborn screening by tandem mass spectrometry for glutaric aciduria type 1: a cost-effectiveness analysis by Pfeil, Johannes (Author) , Listl, Stefan (Author) , Hoffmann, Georg F. (Author) , Kölker, Stefan (Author) , Lindner, Martin (Author) , Burgard, Peter (Author) ,

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