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Neurogenetics

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Open Access 01-07-2010 | LETTER TO THE EDITORS

Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome

Authors: Michael Klintschar, Christian Heimbold

Published in: Neurogenetics | Issue 3/2010

Excerpt

Sirs, …

Filonzi L, Magnani C, Lavezzi AM, Rindi G, Parmigiani S, Bevilacqua G, Matturri L, Marzano FN (2009) Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis. Neurogenetics 10(1):65–72CrossRefPubMed

Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L (2008) Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome. Genomics 91(6):485–491CrossRefPubMed

Poetsch M, Nottebaum BJ, Wingenfeld L, Frede S, Vennemann M, Bajanowski T (2010) Impact of sodium/proton exchanger 3 gene variants on sudden infant death syndrome. J Pediatr 156(1):44–48CrossRefPubMed

Klintschar M, Reichenpfader B (2008) Saternus KS (2008) A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome. J Pediatr 153(2):190–193CrossRefPubMed

Mage DT, Donner M (2004) The X-linkage hypotheses for SIDS and the male excess in infant mortality. Med Hypotheses 62(4):564–567CrossRefPubMed

Title: Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome
Authors: Michael Klintschar
Christian Heimbold
Publication date: 01-07-2010
Publisher: Springer-Verlag
Published in: Neurogenetics / Issue 3/2010
Print ISSN: 1364-6745
Electronic ISSN: 1364-6753
DOI: https://doi.org/10.1007/s10048-010-0242-9

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Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome

Excerpt

Keynote webinar | Spotlight on medication adherence

Springer Medicine

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