Literature DB >> 12112771

Neural basis of prosopagnosia: an fMRI study.

Nouchine Hadjikhani1, Beatrice de Gelder.   

Abstract

Brain imaging research has identified at least two regions in human extrastriate cortex responding selectively to faces. One of these is located in the mid-fusiform gyrus (FFA), the other in the inferior occipital gyrus (IOG). We studied activation of these areas using fMRI in three individuals with severely impaired face recognition (one pure developmental and two childhood prosopagnosics). None of the subjects showed the normal pattern of higher fMRI activity to faces than to objects in the FFA and IOG or elsewhere. Moreover, in two of the patients, faces and objects produced similar activations in the regions corresponding to where the FFA and IOG are found in normal subjects. Our study casts light on the important role of FFA and IOG in the network of areas involved in face recognition, and indicates limits of brain plasticity. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12112771      PMCID: PMC6871884          DOI: 10.1002/hbm.10043

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


  36 in total

1.  Neuroperception. Early visual experience and face processing.

Authors:  R Le Grand; C J Mondloch; D Maurer; H P Brent
Journal:  Nature       Date:  2001-04-19       Impact factor: 49.962

2.  Distinct representations of eye gaze and identity in the distributed human neural system for face perception.

Authors:  E A Hoffman; J V Haxby
Journal:  Nat Neurosci       Date:  2000-01       Impact factor: 24.884

3.  Center-periphery organization of human object areas.

Authors:  I Levy; U Hasson; G Avidan; T Hendler; R Malach
Journal:  Nat Neurosci       Date:  2001-05       Impact factor: 24.884

4.  Selective averaging of rapidly presented individual trials using fMRI.

Authors:  A M Dale; R L Buckner
Journal:  Hum Brain Mapp       Date:  1997       Impact factor: 5.038

5.  The distributed human neural system for face perception.

Authors: 
Journal:  Trends Cogn Sci       Date:  2000-06       Impact factor: 20.229

6.  Inversion superiority in visual agnosia may be common to a variety of orientation polarised objects besides faces.

Authors:  B de Gelder; A C Bachoud-Lévi; J D Degos
Journal:  Vision Res       Date:  1998-09       Impact factor: 1.886

7.  Impairment in facial recognition in patients with cerebral disease.

Authors:  A L Benton; M W Van Allen
Journal:  Trans Am Neurol Assoc       Date:  1968

8.  Configural face processes in acquired and developmental prosopagnosia: evidence for two separate face systems?

Authors:  B de Gelder; R Rouw
Journal:  Neuroreport       Date:  2000-09-28       Impact factor: 1.837

9.  Location of human face-selective cortex with respect to retinotopic areas.

Authors:  E Halgren; A M Dale; M I Sereno; R B Tootell; K Marinkovic; B R Rosen
Journal:  Hum Brain Mapp       Date:  1999       Impact factor: 5.038

10.  Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging.

Authors:  R B Tootell; J B Reppas; K K Kwong; R Malach; R T Born; T J Brady; B R Rosen; J W Belliveau
Journal:  J Neurosci       Date:  1995-04       Impact factor: 6.167

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  36 in total

1.  A modulatory role for facial expressions in prosopagnosia.

Authors:  Beatrice de Gelder; Ilja Frissen; Jason Barton; Nouchine Hadjikhani
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-15       Impact factor: 11.205

Review 2.  Processing faces and facial expressions.

Authors:  Mette T Posamentier; Hervé Abdi
Journal:  Neuropsychol Rev       Date:  2003-09       Impact factor: 7.444

3.  Gaze behaviour in hereditary prosopagnosia.

Authors:  Gudrun Schwarzer; Susanne Huber; Martina Grüter; Thomas Grüter; Cornelia Gross; Melanie Hipfel; Ingo Kennerknecht
Journal:  Psychol Res       Date:  2006-06-10

4.  Impaired face and body perception in developmental prosopagnosia.

Authors:  Ruthger Righart; Beatrice de Gelder
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-17       Impact factor: 11.205

5.  Reduced structural connectivity in ventral visual cortex in congenital prosopagnosia.

Authors:  Cibu Thomas; Galia Avidan; Kate Humphreys; Kwan-jin Jung; Fuqiang Gao; Marlene Behrmann
Journal:  Nat Neurosci       Date:  2008-11-23       Impact factor: 24.884

6.  Individual faces elicit distinct response patterns in human anterior temporal cortex.

Authors:  Nikolaus Kriegeskorte; Elia Formisano; Bettina Sorger; Rainer Goebel
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-11       Impact factor: 11.205

7.  The contribution of the fusiform gyrus and superior temporal sulcus in processing facial attractiveness: neuropsychological and neuroimaging evidence.

Authors:  G Iaria; C J Fox; C T Waite; I Aharon; J J S Barton
Journal:  Neuroscience       Date:  2008-06-08       Impact factor: 3.590

8.  Dedifferentiated face processing in older adults is linked to lower resting state metabolic activity in fusiform face area.

Authors:  Leslie Zebrowitz; Noreen Ward; Jasmine Boshyan; Angela Gutchess; Nouchine Hadjikhani
Journal:  Brain Res       Date:  2016-05-06       Impact factor: 3.252

9.  Role of fusiform and anterior temporal cortical areas in facial recognition.

Authors:  Shahin Nasr; Roger B H Tootell
Journal:  Neuroimage       Date:  2012-08-21       Impact factor: 6.556

Review 10.  Beyond the FFA: The role of the ventral anterior temporal lobes in face processing.

Authors:  Jessica A Collins; Ingrid R Olson
Journal:  Neuropsychologia       Date:  2014-06-14       Impact factor: 3.139

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