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1 e primary motor cortex and to its underlying somatotopic organization.
2 iveness to cutaneous stimuli and patterns of somatotopic organization.
3  dorsal horn cell receptive fields (RFs) and somatotopic organization.
4 isual processes, but no work was done on its somatotopic organization.
5  part of the ipsilateral pRN, reflecting its somatotopic organization.
6 e three facial stimulation sites exhibited a somatotopic organization along the longitudinal (rostroc
7                            The revelation of somatotopic organization and intensity dependency in dri
8                   This study aims to explore somatotopic organization and neural coding in the telenc
9 ts treated with MAM on E33 demonstrated that somatotopic organization and receptive field size are no
10 e responsiveness, receptive field locations, somatotopic organization, and spatial properties of repr
11                        In the present study, somatotopic organization, architectonic features, and pa
12 a preservation of tactile responsiveness and somatotopic organization but, in addition, involves tran
13                              Retinotopic and somatotopic organizations have been described in the cla
14 erminals in the neostriatum followed a crude somatotopic organization in which the amount of overlap
15            The neuroanatomical basis of this somatotopic organization is, however, unknown.
16           Because of the spinal motoneuronal somatotopic organization, motor coordination implies int
17 iological recording techniques to assess the somatotopic organization of brainstem and thalamic areas
18 rpinned by maladaptive neural changes to the somatotopic organization of finger representations withi
19 admill locomotion, 3 min/d, 5 d/week) on the somatotopic organization of forelimb and hindlimb somato
20 ges, surprisingly, we found that there is no somatotopic organization of motor units.
21                                          The somatotopic organization of somatosensory cortex of the
22 nnections, which appear to be woven into the somatotopic organization of the forelimb representation.
23                       In order to reveal the somatotopic organization of the gracile nucleus of the d
24                                          The somatotopic organization of the lateral striatum has bee
25 exact location of the neck motor area in the somatotopic organization of the motor homunculus is stil
26 s in the nodose MEA to determine if there is somatotopic organization of the neurons in that ganglion
27 rtially fits into the traditional concept of somatotopic organization of the nucleus.
28 nfirm the previously postulated ipsilateral, somatotopic organization of the sheep's sensory cortex.
29 ed a qualitatively and quantitatively normal somatotopic organization of vibrissae follicle input to
30 ed sagittal orientation, in keeping with the somatotopic organization present in the pattern of prima
31 ties of coherence indicate a differentiated, somatotopic organization; so far, however, little attent
32 two fields that corresponded in location and somatotopic organization to the second somatosensory are
33               To investigate conservation of somatotopic organization, we compared trigeminal nerve o
34                                   To examine somatotopic organization, we separately stimulated the l