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1 iveness to cutaneous stimuli and patterns of somatotopic organization.
2 dorsal horn cell receptive fields (RFs) and somatotopic organization.
3 e primary motor cortex and to its underlying somatotopic organization.
4 e three facial stimulation sites exhibited a somatotopic organization along the longitudinal (rostroc
5 ts treated with MAM on E33 demonstrated that somatotopic organization and receptive field size are no
6 e responsiveness, receptive field locations, somatotopic organization, and spatial properties of repr
8 a preservation of tactile responsiveness and somatotopic organization but, in addition, involves tran
10 erminals in the neostriatum followed a crude somatotopic organization in which the amount of overlap
12 iological recording techniques to assess the somatotopic organization of brainstem and thalamic areas
13 admill locomotion, 3 min/d, 5 d/week) on the somatotopic organization of forelimb and hindlimb somato
18 exact location of the neck motor area in the somatotopic organization of the motor homunculus is stil
20 nfirm the previously postulated ipsilateral, somatotopic organization of the sheep's sensory cortex.
21 ed a qualitatively and quantitatively normal somatotopic organization of vibrissae follicle input to
22 ed sagittal orientation, in keeping with the somatotopic organization present in the pattern of prima
23 ties of coherence indicate a differentiated, somatotopic organization; so far, however, little attent
24 two fields that corresponded in location and somatotopic organization to the second somatosensory are
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