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Journal Abstract Search

267 related items for PubMed ID: 18477062

  • 1.
    ; . PubMed ID:
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  • 2. 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. PubMed ID: 18387780
    [Abstract] [Full Text] [Related]

  • 3. IL-1 gene cluster polymorphisms and sudden infant death syndrome.
    Ferrante L, Opdal SH, Vege A, Rognum TO.
    Hum Immunol; 2010 Apr; 71(4):402-6. PubMed ID: 20080142
    [Abstract] [Full Text] [Related]

  • 4. [Association study of sleep apnea syndrome and polymorphisms in the serotonin transporter gene].
    Yue WH, Liu PZ, Hao W, Zhang XH, Wang XP, Zhang JS, Zhou XH, Xie YB, Ni M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Oct; 22(5):533-6. PubMed ID: 16215942
    [Abstract] [Full Text] [Related]

  • 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. PubMed ID: 24286237
    [Abstract] [Full Text] [Related]

  • 6. Cytokine gene polymorphisms and sudden infant death syndrome.
    Ferrante L, Opdal SH, Vege A, Rognum T.
    Acta Paediatr; 2010 Mar; 99(3):384-8. PubMed ID: 19958302
    [Abstract] [Full Text] [Related]

  • 7. 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. PubMed ID: 22711722
    [Abstract] [Full Text] [Related]

  • 8. Serotonin transporter promoter and intron 2 polymorphisms: relationship between allelic variants and gene expression.
    Hranilovic D, Stefulj J, Schwab S, Borrmann-Hassenbach M, Albus M, Jernej B, Wildenauer D.
    Biol Psychiatry; 2004 Jun 01; 55(11):1090-4. PubMed ID: 15158428
    [Abstract] [Full Text] [Related]

  • 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. PubMed ID: 12966525
    [Abstract] [Full Text] [Related]

  • 10. The sudden infant death syndrome gene: does it exist?
    Opdal SH, Rognum TO.
    Pediatrics; 2004 Oct 15; 114(4):e506-12. PubMed ID: 15466077
    [Abstract] [Full Text] [Related]

  • 11. Serotonin transporter gene promoter (5-HTTLPR) and intron 2 (VNTR) polymorphisms: a study on Slovenian population of suicide victims.
    Pungercic G, Videtic A, Pestotnik A, Pajnic IZ, Zupanc T, Balazic J, Tomori M, Komel R.
    Psychiatr Genet; 2006 Oct 15; 16(5):187-91. PubMed ID: 16969272
    [Abstract] [Full Text] [Related]

  • 12. Serotonin transporter polymorphism in Croatian patients with major depressive disorder.
    Bozina N, Mihaljević-Peles A, Sagud M, Jakovljević M, Sertić J.
    Psychiatr Danub; 2006 Jun 15; 18(1-2):83-9. PubMed ID: 16804504
    [Abstract] [Full Text] [Related]

  • 13. Investigation of 5-HTT expression using quantitative real-time PCR in the human brain in SIDS Italian cases.
    Casale V, Oneda R, Matturri L, Lavezzi AM.
    Exp Mol Pathol; 2013 Feb 15; 94(1):239-42. PubMed ID: 22771822
    [Abstract] [Full Text] [Related]

  • 14. Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism.
    Lavezzi AM, Casale V, Oneda R, Weese-Mayer DE, Matturri L.
    Pediatr Res; 2009 Jul 15; 66(1):22-7. PubMed ID: 19342987
    [Abstract] [Full Text] [Related]

  • 15. The IL6 -174G/C polymorphism and sudden infant death syndrome.
    Opdal SH, Rognum TO.
    Hum Immunol; 2007 Jun 15; 68(6):541-3. PubMed ID: 17509454
    [Abstract] [Full Text] [Related]

  • 16. Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy.
    Manna I, Labate A, Gambardella A, Forabosco P, La Russa A, Le Piane E, Aguglia U, Quattrone A.
    Neurosci Lett; 2007 Jun 21; 421(1):52-6. PubMed ID: 17548158
    [Abstract] [Full Text] [Related]

  • 17. Association of serotonin transporter gene polymorphism with obstructive sleep apnea syndrome.
    Ylmaz M, Bayazit YA, Ciftci TU, Erdal ME, Urhan M, Kokturk O, Kemaloglu YK, Inal E.
    Laryngoscope; 2005 May 21; 115(5):832-6. PubMed ID: 15867649
    [Abstract] [Full Text] [Related]

  • 18. Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation.
    Pfisterer N, Meyer-Bockenkamp F, Qu D, Preuss V, Rothämel T, Geisenberger D, Läer K, Vennemann B, Albers A, Engelmann TA, Frieling H, Rhein M, Klintschar M.
    Pediatr Res; 2022 Sep 21; 92(3):694-699. PubMed ID: 34764460
    [Abstract] [Full Text] [Related]

  • 19. TNF-alpha promoter polymorphisms in sudden infant death.
    Ferrante L, Opdal SH, Vege A, Rognum TO.
    Hum Immunol; 2008 Jun 21; 69(6):368-73. PubMed ID: 18571009
    [Abstract] [Full Text] [Related]

  • 20. 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. PubMed ID: 12599191
    [Abstract] [Full Text] [Related]

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