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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

508 related items for PubMed ID: 16930564

  • 41. A network of occipito-temporal face-sensitive areas besides the right middle fusiform gyrus is necessary for normal face processing.
    Rossion B, Caldara R, Seghier M, Schuller AM, Lazeyras F, Mayer E.
    Brain; 2003 Nov; 126(Pt 11):2381-95. PubMed ID: 12876150
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  • 42. Inversion and contrast polarity reversal affect both encoding and recognition processes of unfamiliar faces: a repetition study using ERPs.
    Itier RJ, Taylor MJ.
    Neuroimage; 2002 Feb; 15(2):353-72. PubMed ID: 11798271
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  • 48. Configural processing of other-race faces is delayed but not decreased.
    Wiese H, Stahl J, Schweinberger SR.
    Biol Psychol; 2009 May; 81(2):103-9. PubMed ID: 19428974
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  • 51. Top-down activation of fusiform cortex without seeing faces in prosopagnosia.
    Righart R, Andersson F, Schwartz S, Mayer E, Vuilleumier P.
    Cereb Cortex; 2010 Aug; 20(8):1878-90. PubMed ID: 19939884
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  • 52. The fusiform face area and occipital face area show sensitivity to spatial relations in faces.
    Rhodes G, Michie PT, Hughes ME, Byatt G.
    Eur J Neurosci; 2009 Aug; 30(4):721-33. PubMed ID: 19674084
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  • 56. MEG/EEG sources of the 170-ms response to faces are co-localized in the fusiform gyrus.
    Deffke I, Sander T, Heidenreich J, Sommer W, Curio G, Trahms L, Lueschow A.
    Neuroimage; 2007 May 01; 35(4):1495-501. PubMed ID: 17363282
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  • 57. Rapid adaptation of the m170 response: importance of face parts.
    Harris A, Nakayama K.
    Cereb Cortex; 2008 Feb 01; 18(2):467-76. PubMed ID: 17573371
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  • 60. N250 ERP correlates of the acquisition of face representations across different images.
    Kaufmann JM, Schweinberger SR, Burton AM.
    J Cogn Neurosci; 2009 Apr 01; 21(4):625-41. PubMed ID: 18702593
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