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Results: 1 to 20 of 106

Similar articles for PubMed (Select 21265843)

1.

Significant association of TH01 allele 9.3 and SIDS.

Courts C, Madea B.

J Forensic Sci. 2011 Mar;56(2):415-7. doi: 10.1111/j.1556-4029.2010.01670.x. Epub 2011 Jan 25.

PMID:
21265843
2.

A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome.

Klintschar M, Reichenpfader B, Saternus KS.

J Pediatr. 2008 Aug;153(2):190-3. doi: 10.1016/j.jpeds.2008.02.032. Epub 2008 Apr 3.

PMID:
18534229
3.

No association of IL-10 promoter SNP -592 and -1082 and SIDS.

Courts C, Madea B.

Forensic Sci Int. 2011 Jan 30;204(1-3):179-81. doi: 10.1016/j.forsciint.2010.06.001. Epub 2010 Jun 29.

PMID:
20591588
4.

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
5.

A common FMO3 polymorphism may amplify the effect of nicotine exposure in sudden infant death syndrome (SIDS).

Poetsch M, Czerwinski M, Wingenfeld L, Vennemann M, Bajanowski T.

Int J Legal Med. 2010 Jul;124(4):301-6. doi: 10.1007/s00414-010-0428-6. Epub 2010 Mar 3.

PMID:
20198379
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.

A controlled study of the relationship between Bordetella pertussis infections and sudden unexpected deaths among German infants.

Heininger U, Kleemann WJ, Cherry JD; Sudden Infant Death Syndrome Study Group.

Pediatrics. 2004 Jul;114(1):e9-15.

PMID:
15231967
9.
10.

Apolipoprotein E e4 and its prevalence in early childhood death due to sudden infant death syndrome or to recognised causes.

Becher JC, Keeling JW, Bell J, Wyatt B, McIntosh N.

Early Hum Dev. 2008 Aug;84(8):549-54. doi: 10.1016/j.earlhumdev.2008.01.002. Epub 2008 Feb 20.

PMID:
18280677
11.

Association of IL-10 genotype with sudden infant death syndrome.

Summers AM, Summers CW, Drucker DB, Hajeer AH, Barson A, Hutchinson IV.

Hum Immunol. 2000 Dec;61(12):1270-3.

PMID:
11163082
12.

Variant interleukin 1 receptor antagonist gene alleles in sudden infant death syndrome.

Highet AR, Gibson CS, Goldwater PN.

Arch Dis Child. 2010 Dec;95(12):1009-12. doi: 10.1136/adc.2010.188268. Epub 2010 Sep 29.

PMID:
20880945
13.

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
14.

Positive association of tyrosine hydroxylase microsatellite marker to essential hypertension.

Sharma P, Hingorani A, Jia H, Ashby M, Hopper R, Clayton D, Brown MJ.

Hypertension. 1998 Oct;32(4):676-82.

15.

The G protein beta3 subunit 825C allele is associated with sudden infant death due to infection.

Hauge Opdal S, Melien Ø, Rootwelt H, Vege A, Arnestad M, Ole Rognum T.

Acta Paediatr. 2006 Sep;95(9):1129-32.

PMID:
16938762
16.

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.

17.

Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians.

Studer J, Bartsch C, Haas C.

J Forensic Sci. 2014 Nov;59(6):1650-3. doi: 10.1111/1556-4029.12526. Epub 2014 Jun 27.

PMID:
24975687
18.

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.

19.
20.

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
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