Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Sudden Infant Death and MAOA[original query] |
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| Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis. Neurogenetics 2009 Feb 10 (1): 65-72. Filonzi Laura, Magnani Cinzia, Lavezzi Anna Maria, Rindi Guido, Parmigiani Stefano, Bevilacqua Giulio, Matturri Luigi, Marzano Francesco Nonn |
| Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE. Pediatrics 2012 Jul 130 (1): e138-44. Filonzi Laura, Magnani Cinzia, Nosetti Luana, Nespoli Luigi, Borghi Camilla, Vaghi Marina, Nonnis Marzano Frances |
| Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome. Pediatrics 2012 Mar 129 (3): e756-61. Klintschar Michael, Heimbold Christi |
| Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit. International journal of legal medicine 2014 Jan 128 (1): 43-9. Groß Maximilian, Bajanowski Thomas, Vennemann Mechtild, Poetsch Micae |
| Association between monoamine oxidase A promoter polymorphism and the risk of sudden infant death syndrome: a meta-analysis. International journal of legal medicine 2021 Feb . Zhou Qiaoxia, Gong Daoyin, Zhang Yu, Huang Feij |
- Page last reviewed:Feb 1, 2024
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