Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE.

Pediatrics - 1 Jul 2012

Filonzi Laura, Magnani Cinzia, Nosetti Luana, Nespoli Luigi, Borghi Camilla, Vaghi Marina, Nonnis Marzano Francesco

Abstract excerpt

OBJECTIVE: Considering previous genetic studies on sudden infant death syndrome (SIDS) and the role of L/L serotonin transporter (5HTT) genotype and correlated genes monoamine oxidase A (MAOA) and dopamine transporter (DAT) in unexpected death, an investigation was carried out verifying their involvement in apparent life-threatening events (ALTE and idiopathic form [IALTE]), also assessing common molecular basis...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Dopamine Plasma Membrane Transport Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Infant

Share to Infant, Newborn

Share to Monoamine Oxidase

Share to Serotonin Plasma Membrane Transport Proteins

Share to Sudden Infant Death

Source

Identifiers

PMID: 22711722
DOI: 10.1542/peds.2011-3331

Genes

MAOA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE.PMID 22711722Read ↗

Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis.Semantic proximity Read ↗

A serotonin malfunction hypothesis by finding clear mutual relationships between several risk factors and symptoms associated with sudden infant death syndrome.Semantic proximity Read ↗

Serotonin transporter gene variation in sudden infant death syndrome.Semantic proximity Read ↗

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.Semantic proximity Read ↗

Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation.Semantic proximity Read ↗

Sudden death of an infant with cardiac, nervous system and genetic involvement--a case report.Semantic proximity Read ↗

Gene variants predisposing to SIDS: current knowledge.Semantic proximity Read ↗

Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population.Semantic proximity Read ↗

Sudden Infant Death Syndrome: review of implicated genetic factors.Semantic proximity Read ↗

Serotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome.Semantic proximity Read ↗

Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit.Semantic proximity Read ↗

HTR2A variation and sudden infant death syndrome: a case-control analysis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.