ライフサイエンスコーパス: prosopagnosia

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1 abilities in individuals with developmental prosopagnosia.

2 ed by individuals who suffer from congenital prosopagnosia.

3 d the focal clinical syndrome of progressive prosopagnosia.

4 erior temporo-occipital damage can result in prosopagnosia.

5 as autism spectrum disorders and congenital prosopagnosia.

6 A Quick guide to developmental prosopagnosia, a condition definied by problems in recog

7 ughly 2% of the population has developmental prosopagnosia, a congenital deficit in recognizing other

8 Furthermore, people with developmental prosopagnosia, a lifelong face recognition impairment, h

9 ffecting gaze behavior toward faces, such as prosopagnosia and autism spectrum disorders.

10 s: subjects with a face recognition deficit (prosopagnosia) and matched controls.

11 for covert face recognition in developmental prosopagnosia, and suggest this phenomenon results from

12 mechanisms in individuals with developmental prosopagnosia are not qualitatively different from that

13 Thus, she had no prosopagnosia, but abnormal 'hyperfamiliarity' for unkno

14 One of our prosopagnosia cases exhibited a severe reading impairmen

15 trials where participants with developmental prosopagnosia classified famous faces as known or famili

16 n impairment in face recognition, congenital prosopagnosia (CP), and matched controls.

17 nising faces that, in contrast with acquired prosopagnosia, develop in the absence of manifest brain

18 Developmental prosopagnosia (DP) is characterised by severe deficits i

19 Developmental prosopagnosia (DP) refers to face recognition deficits i

20 Individuals with developmental prosopagnosia (DP), a lifelong face recognition impairme

21 results ruled out all extant explanations of prosopagnosia except one that proposed that faces are re

22 Individuals with developmental prosopagnosia exhibit severe and lasting difficulties in

23 Strikingly, adults with developmental prosopagnosia (face blindness) express an atypical struc

24 Prosopagnosia has largely been regarded as an untreatabl

25 Here we present two cases of acquired prosopagnosia, Herschel and Florence, who violate this p

26 group of 12 participants with developmental prosopagnosia in a task that required them to judge the

27 Developmental prosopagnosia is characterized by severely impaired face

28 argue that the focal syndrome of progressive prosopagnosia is one of the clinical presentations of se

29 ses in the ventral temporal cortex (VTC) and prosopagnosia is reported in patients with lesions in th

30 tients to exhibit associative agnosia and/or prosopagnosia: many authors have used the label SD for p

31 In six individuals with developmental prosopagnosia, non-recognized famous faces triggered an

32 Our results show that a man with severe prosopagnosia performed normally throughout the standard

33 licits modality-specific impairments such as prosopagnosia, pure word blindness and category-specific

34 Many aspects of face processing (e.g., prosopagnosia, recognition, and configural vs. featural

35 visual field defect, visual hallucinations, prosopagnosia, topographical disorientation, disturbance

36 Prosopagnosia was a symptom in right temporal lobe atrop

37 ecognition in individuals with developmental prosopagnosia, we tested a group of 12 participants with

38 Twelve subjects with developmental prosopagnosia were assessed before and after training, a

39 variety of neural profiles in developmental prosopagnosia, which is consistent with behavioral studi

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