Publications by authors named "Christian Heimbold"

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Our lives with PKU: German patient voices - "Nothing about us without us".
Karin Lange, Jens Böhmer, Yvonne Deich, Daniel Dickneite, Pascale Fuchs, Christian Heimbold

Mol Genet Metab Rep· June 2025

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Two years of pegvaliase in Germany: Experiences and best practice recommendations.
Johannes Krämer, Christoph Baerwald, Christian Heimbold, Clemens Kamrath, Klaus G Parhofer

Mol Genet Metab· May 2023

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No association of SIDS with two polymorphisms in genes relevant for the noradrenergic system: COMT and DBH.
Michael Klintschar, Christian Heimbold

Acta Paediatr· October 2012

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Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome.
Michael Klintschar, Christian Heimbold

Pediatrics· March 2012

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Transfer of biological stains from different surfaces.
Peter Wiegand, Christian Heimbold, Rachel Klein, Uta Immel, Dankwart Stiller

Int J Legal Med· September 2011

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Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome.
Michael Klintschar, Christian Heimbold

Neurogenetics· July 2010

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