Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 149

1.

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

Filonzi L, Magnani C, Nosetti L, Nespoli L, Borghi C, Vaghi M, Nonnis Marzano F.

Pediatrics. 2012 Jul;130(1):e138-44. doi: 10.1542/peds.2011-3331. Epub 2012 Jun 18.

2.

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

Filonzi L, Magnani C, Lavezzi AM, Rindi G, Parmigiani S, Bevilacqua G, Matturri L, Marzano FN.

Neurogenetics. 2009 Feb;10(1):65-72. doi: 10.1007/s10048-008-0149-x. Epub 2008 Sep 23.

PMID:
18810510
3.

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

Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L.

Genomics. 2008 Jun;91(6):485-91. doi: 10.1016/j.ygeno.2008.01.010. Epub 2008 Apr 2.

4.

Serotonin transporter gene variation in sudden infant death syndrome.

Opdal SH, Vege A, Rognum TO.

Acta Paediatr. 2008 Jul;97(7):861-5. doi: 10.1111/j.1651-2227.2008.00813.x. Epub 2008 May 12.

PMID:
18477062
5.

Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome.

Opdal SH, Vege Å, Rognum TO.

Acta Paediatr. 2014 Apr;103(4):393-7. doi: 10.1111/apa.12526. Epub 2013 Dec 27.

PMID:
24286237
6.

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.

Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML.

Am J Med Genet A. 2003 Mar 15;117A(3):268-74.

PMID:
12599191
7.

No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians.

Haas C, Braun J, Bär W, Bartsch C.

Leg Med (Tokyo). 2009 Apr;11 Suppl 1:S210-2. doi: 10.1016/j.legalmed.2009.01.051. Epub 2009 Mar 3.

PMID:
19261524
8.

The sudden infant death syndrome gene: does it exist?

Opdal SH, Rognum TO.

Pediatrics. 2004 Oct;114(4):e506-12.

PMID:
15466077
9.

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.

Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML.

Am J Med Genet A. 2003 Oct 15;122A(3):238-45.

PMID:
12966525
10.

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

Groß M, Bajanowski T, Vennemann M, Poetsch M.

Int J Legal Med. 2014 Jan;128(1):43-9. doi: 10.1007/s00414-013-0928-2. Epub 2013 Oct 31.

PMID:
24173666
12.

Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome.

Klintschar M, Heimbold C.

Pediatrics. 2012 Mar;129(3):e756-61. doi: 10.1542/peds.2011-1642. Epub 2012 Feb 20.

13.

Why do ALTE infants not die in SIDS?

Edner A, Wennborg M, Alm B, Lagercrantz H.

Acta Paediatr. 2007 Feb;96(2):191-4.

PMID:
17429903
14.

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

Narita N, Narita M, Takashima S, Nakayama M, Nagai T, Okado N.

Pediatrics. 2001 Apr;107(4):690-2.

PMID:
11335745
15.

Epidemiology of apparent life threatening events.

Kiechl-Kohlendorfer U, Hof D, Peglow UP, Traweger-Ravanelli B, Kiechl S.

Arch Dis Child. 2005 Mar;90(3):297-300.

16.

Alcohol dependence and polymorphisms of serotonin-related genes: association studies.

Mokrović G, Matosić A, Hranilović D, Stefulj J, Novokmet M, Oresković D, Balija M, Marusić S, Cicin-Sain L.

Coll Antropol. 2008 Jan;32 Suppl 1:127-31.

PMID:
18405071
17.

Lack of association of the serotonin transporter polymorphism with the sudden infant death syndrome in the San Diego Dataset.

Paterson DS, Rivera KD, Broadbelt KG, Trachtenberg FL, Belliveau RA, Holm IA, Haas EA, Stanley C, Krous HF, Kinney HC, Markianos K.

Pediatr Res. 2010 Nov;68(5):409-13. doi: 10.1203/PDR.0b013e3181f2edf0.

18.

Mucosal immune responses to infections in infants with acute life threatening events classified as 'near-miss' sudden infant death syndrome.

Gleeson M, Clancy RL, Cox AJ, Gulliver SA, Hall ST, Cooper DM.

FEMS Immunol Med Microbiol. 2004 Sep 1;42(1):105-18.

19.

Monoamine oxidase A gene polymorphism and the pathogenesis of sudden infant death syndrome.

Courts C, Grabmüller M, Madea B.

J Pediatr. 2013 Jul;163(1):89-93. doi: 10.1016/j.jpeds.2012.12.072. Epub 2013 Feb 4.

PMID:
23391042
20.

Associations of MAOA-VNTR or 5HTT-LPR alleles with attention-deficit hyperactivity disorder symptoms are moderated by platelet monoamine oxidase B activity.

Wargelius HL, Malmberg K, Larsson JO, Oreland L.

Psychiatr Genet. 2012 Feb;22(1):42-5. doi: 10.1097/YPG.0b013e328347c1ab.

PMID:
21610556
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk