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1  as autism spectrum disorders and congenital prosopagnosia.
2  abilities in individuals with developmental prosopagnosia.
3 ed by individuals who suffer from congenital prosopagnosia.
4 d the focal clinical syndrome of progressive prosopagnosia.
5 entify connections common to lesions causing prosopagnosia.
6 erior temporo-occipital damage can result in prosopagnosia.
7 ailing diagnostic criteria for developmental prosopagnosia.
8 reproducible and specific to lesions causing prosopagnosia.
9               A Quick guide to developmental prosopagnosia, a condition definied by problems in recog
10 ughly 2% of the population has developmental prosopagnosia, a congenital deficit in recognizing other
11       Furthermore, people with developmental prosopagnosia, a lifelong face recognition impairment, h
12 ffecting gaze behavior toward faces, such as prosopagnosia and autism spectrum disorders.
13 ontal regions were independent predictors of prosopagnosia and predicted subclinical facial agnosia i
14 s: subjects with a face recognition deficit (prosopagnosia) and matched controls.
15 for covert face recognition in developmental prosopagnosia, and suggest this phenomenon results from
16 mechanisms in individuals with developmental prosopagnosia are not qualitatively different from that
17 ce recognition deficits observed in Acquired Prosopagnosia are typically associated with impaired hol
18                             Thus, she had no prosopagnosia, but abnormal 'hyperfamiliarity' for unkno
19                                   One of our prosopagnosia cases exhibited a severe reading impairmen
20 trials where participants with developmental prosopagnosia classified famous faces as known or famili
21 ork derived from clinically evident cases of prosopagnosia could predict subclinical facial agnosia i
22 n impairment in face recognition, congenital prosopagnosia (CP), and matched controls.
23 nising faces that, in contrast with acquired prosopagnosia, develop in the absence of manifest brain
24                                Developmental prosopagnosia (DP) is a condition characterised by lifel
25                                Developmental prosopagnosia (DP) is a neurodevelopmental condition cha
26                                Developmental prosopagnosia (DP) is characterised by deficits in face
27                                Developmental prosopagnosia (DP) is characterised by severe deficits i
28                                Developmental prosopagnosia (DP) refers to face recognition deficits i
29               Individuals with developmental prosopagnosia (DP), a lifelong face recognition impairme
30                                              Prosopagnosia, episodic memory impairment and behavioura
31 results ruled out all extant explanations of prosopagnosia except one that proposed that faces are re
32               Individuals with developmental prosopagnosia exhibit severe and lasting difficulties in
33        Strikingly, adults with developmental prosopagnosia (face blindness) express an atypical struc
34 as previously been described as memory loss, prosopagnosia, getting lost and behavioural changes.
35                                              Prosopagnosia has largely been regarded as an untreatabl
36        Here we present two cases of acquired prosopagnosia, Herschel and Florence, who violate this p
37  group of 12 participants with developmental prosopagnosia in a task that required them to judge the
38  and the fusiform gyrus were associated with prosopagnosia in rtvFTD.
39                                Developmental prosopagnosia is characterized by severely impaired face
40 argue that the focal syndrome of progressive prosopagnosia is one of the clinical presentations of se
41 ses in the ventral temporal cortex (VTC) and prosopagnosia is reported in patients with lesions in th
42 cells from occipitotemporal inputs may yield prosopagnosia-like symptoms.
43             We conclude that lesions causing prosopagnosia localize to a single functionally connecte
44 tients to exhibit associative agnosia and/or prosopagnosia: many authors have used the label SD for p
45 hat holistic processing deficits in Acquired Prosopagnosia may be task-specific and persist over time
46  lesions associated with symptoms other than prosopagnosia (n = 155).
47        In six individuals with developmental prosopagnosia, non-recognized famous faces triggered an
48 erature search identified 44 lesions causing prosopagnosia, only 29 of which intersected the right fu
49 of holistic processing in a case of acquired prosopagnosia (Patient DS).
50      Our results show that a man with severe prosopagnosia performed normally throughout the standard
51 modal learning in modality-specific agnosia (prosopagnosia, phonagnosia).
52 licits modality-specific impairments such as prosopagnosia, pure word blindness and category-specific
53       Many aspects of face processing (e.g., prosopagnosia, recognition, and configural vs. featural
54 de participants with extreme behavior (e.g., prosopagnosia, super-recognizers), and does not accommod
55 neral population, ranging from developmental prosopagnosia to "super-recognizers".
56  visual field defect, visual hallucinations, prosopagnosia, topographical disorientation, disturbance
57                                              Prosopagnosia was a symptom in right temporal lobe atrop
58 ecognition in individuals with developmental prosopagnosia, we tested a group of 12 participants with
59           Twelve subjects with developmental prosopagnosia were assessed before and after training, a
60                            Cases of acquired prosopagnosia were identified through a systematic liter
61  variety of neural profiles in developmental prosopagnosia, which is consistent with behavioral studi