All Relations between spindle-shaped and area temporalis inferior

Publication Sentence Publish Date Extraction Date Species
N C Andreasen, D S O'Leary, S Arndt, T Cizadlo, R Hurtig, K Rezai, G L Watkins, L B Ponto, R D Hichw. Neural substrates of facial recognition. The Journal of neuropsychiatry and clinical neurosciences. vol 8. issue 2. 1997-04-03. PMID:9081548. these tasks activated three different pathways: respectively, the left inferior temporal lobe and left frontal cortex; a predominantly right frontal-right parietal-left cerebellar network; and left lingual and left and right fusiform gyri. 1997-04-03 2023-08-12 human
J R Binder, J A Frost, T A Hammeke, R W Cox, S M Rao, T Priet. Human brain language areas identified by functional magnetic resonance imaging. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 17. issue 1. 1997-02-04. PMID:8987760. less consistent with classical models were (1) the existence of left hemisphere temporoparietal language areas outside the traditional "wernicke area," namely, in the middle temporal, inferior temporal, fusiform, and angular gyri; (2) extensive left prefrontal language areas outside the classical "broca area"; and (3) clear participation of these left frontal areas in a task emphasizing "receptive" language functions. 1997-02-04 2023-08-12 human
A Puce, T Allison, J C Gore, G McCarth. Face-sensitive regions in human extrastriate cortex studied by functional MRI. Journal of neurophysiology. vol 74. issue 3. 1996-01-18. PMID:7500143. activated voxels to faces were obtained in the fusiform and inferior temporal gyri in 9 of 12 subjects and were approximately coextensive with previously identified face-selective regions. 1996-01-18 2023-08-12 human
P E Roland, B Gulyá. Visual memory, visual imagery, and visual recognition of large field patterns by the human brain: functional anatomy by positron emission tomography. Cerebral cortex (New York, N.Y. : 1991). vol 5. issue 1. 1995-05-24. PMID:7719132. perception and learning of the patterns increased rcbf in v1 and 17 cortical fields located in the cuneus, the lingual, fusiform, inferior temporal, occipital, and angular gyri, the precuneus, and the posterior part of superior parietal lobules. 1995-05-24 2023-08-12 human
T Allison, G McCarthy, A Nobre, A Puce, A Belge. Human extrastriate visual cortex and the perception of faces, words, numbers, and colors. Cerebral cortex (New York, N.Y. : 1991). vol 4. issue 5. 1995-02-24. PMID:7833655. n200 was recorded bilaterally from discrete regions of the fusiform and inferior temporal gyri. 1995-02-24 2023-08-12 human
B Gulyás, C A Heywood, D A Popplewell, P E Roland, A Cowe. Visual form discrimination from color or motion cues: functional anatomy by positron emission tomography. Proceedings of the National Academy of Sciences of the United States of America. vol 91. issue 21. 1994-11-10. PMID:7937927. the discrimination of form by means of motion cues activated functional fields bilaterally in the inferior and lateral occipital gyri, in the lingual, anterior cingulate, middle frontal and orbitofrontal gyri, and in the left fusiform and right inferior temporal gyri. 1994-11-10 2023-08-12 human
Y Sakurai, K Sakai, M Sakuta, M Iwat. Naming difficulties in alexia with agraphia for kanji after a left posterior inferior temporal lesion. Journal of neurology, neurosurgery, and psychiatry. vol 57. issue 5. 1994-07-07. PMID:8201334. magnetic resonance imaging at four months after onset showed a lesion in the inferior temporal and fusiform gyri, extending from the temporo-occipital junction toward the anterior third of the temporal lobe. 1994-07-07 2023-08-12 Not clear
Y Sakurai, K Sakai, M Sakuta, M Iwat. Naming difficulties in alexia with agraphia for kanji after a left posterior inferior temporal lesion. Journal of neurology, neurosurgery, and psychiatry. vol 57. issue 5. 1994-07-07. PMID:8201334. it is suggested that the disconnection of association fibres between the parahippocampal, fusiform, middle, and inferior temporal gyri, especially between the parahippocampal gyrus and the other temporal gyri, or the cortical damage to the posterior part of these gyri is essential for the production of anomia. 1994-07-07 2023-08-12 Not clear
T Allison, H Ginter, G McCarthy, A C Nobre, A Puce, M Luby, D D Spence. Face recognition in human extrastriate cortex. Journal of neurophysiology. vol 71. issue 2. 1994-06-09. PMID:8176446. n200 was recorded only from small regions of the left and right fusiform and inferior temporal gyri. 1994-06-09 2023-08-12 human
N Kawahata, K Nagat. A case of associative visual agnosia: neuropsychological findings and theoretical considerations. Journal of clinical and experimental neuropsychology. vol 11. issue 5. 1989-12-07. PMID:2808655. mri demonstrated extensive low-intensity lesions in the lingual, fusiform and posterior inferior temporal gyri on both hemispheres. 1989-12-07 2023-08-11 Not clear
A M Palmer, G C Stratmann, A W Procter, D M Bowe. Possible neurotransmitter basis of behavioral changes in Alzheimer's disease. Annals of neurology. vol 23. issue 6. 1988-09-16. PMID:2457353. the dopamine metabolite was not reduced in any area, whereas both indoleamines were reduced in the superior frontal, inferior temporal, and fusiform gyri, and the temporal pole. 1988-09-16 2023-08-11 human