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Title
Gene variants predisposing to SIDS: current knowledge
Authors
Keywords
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Journal
Forensic Science Medicine and Pathology
Volume 7, Issue 1, Pages 26-36
Publisher
Springer Nature
Online
2010-07-12
DOI
10.1007/s12024-010-9182-9
References
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Note: Only part of the references are listed.- Distribution of interleukin-1 receptor antagonist genotypes in Sudden Unexpected Death in Infancy (SUDI); unexplained SUDI have a higher frequency of allele 2
- (2010) Amanda R. Highet et al. ANNALS OF MEDICINE
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- Brainstem Serotonergic Deficiency in Sudden Infant Death Syndrome
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- Interleukin-6 and the serotonergic system of the medulla oblongata in the sudden infant death syndrome
- (2009) Ingvar Jon Rognum et al. ACTA NEUROPATHOLOGICA
- The Brainstem and Serotonin in the Sudden Infant Death Syndrome
- (2009) Hannah C. Kinney et al. Annual Review of Pathology-Mechanisms of Disease
- α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current
- (2009) Jianding Cheng et al. Circulation-Arrhythmia and Electrophysiology
- Copy number variations in three children with sudden infant death
- (2009) GA Toruner et al. CLINICAL GENETICS
- No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians
- (2009) Cordula Haas et al. Legal Medicine
- SNP association and sequence analysis of the NOS1AP gene in SIDS
- (2009) Motoki Osawa et al. Legal Medicine
- Contribution of Long-QT Syndrome Genetic Variants in Sudden Infant Death Syndrome
- (2009) Gilles Millat et al. PEDIATRIC CARDIOLOGY
- Serotonin-Related FEV Gene Variant in the Sudden Infant Death Syndrome Is a Common Polymorphism in the African-American Population
- (2009) Kevin G Broadbelt et al. PEDIATRIC RESEARCH
- Sudden Infant Death Syndrome and Sudden Intrauterine Unexplained Death: Correlation Between Hypoplasia of Raphé Nuclei and Serotonin Transporter Gene Promoter Polymorphism
- (2009) Anna M Lavezzi et al. PEDIATRIC RESEARCH
- Medullary serotonin defects and respiratory dysfunction in sudden infant death syndrome
- (2009) David S. Paterson et al. RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY
- Serotonin transporter gene variation in sudden infant death syndrome
- (2008) Siri Hauge Opdal et al. ACTA PAEDIATRICA
- Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP)
- (2008) Kevin J Cummings et al. ACTA PAEDIATRICA
- Surfactant protein A and D gene polymorphisms and protein expression in victims of sudden infant death
- (2008) Arne Stray-Pedersen et al. ACTA PAEDIATRICA
- HTR2Avariation and sudden infant death syndrome: a case-control analysis
- (2008) Casey M Rand et al. ACTA PAEDIATRICA
- Genetic variation in theHTR1A gene and sudden infant death syndrome
- (2008) Megan E. Morley et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Apolipoprotein E e4 and its prevalence in early childhood death due to sudden infant death syndrome or to recognised causes
- (2008) Julie-Clare Becher et al. EARLY HUMAN DEVELOPMENT
- TNF-α AND IL-10 GENE POLYMORPHISMS VERSUS CARDIOIMMUNOLOGICAL RESPONSES IN SUDDEN INFANT DEATH
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- (2008) Francesco Nonnis Marzano et al. GENOMICS
- Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome
- (2008) David W. Van Norstrand et al. HEART RHYTHM
- TNF-α promoter polymorphisms in sudden infant death
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- A Functional Polymorphism in the Tyrosine Hydroxylase Gene Indicates a Role of Noradrenalinergic Signaling in Sudden Infant Death Syndrome
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