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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
7                        In the present study, somatotopic organization, architectonic features, and pa
8 a preservation of tactile responsiveness and somatotopic organization but, in addition, involves tran
9                              Retinotopic and somatotopic organizations have been described in the cla
10 erminals in the neostriatum followed a crude somatotopic organization in which the amount of overlap
11           Because of the spinal motoneuronal somatotopic organization, motor coordination implies int
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
14 ges, surprisingly, we found that there is no somatotopic organization of motor units.
15                                          The somatotopic organization of somatosensory cortex of the
16                       In order to reveal the somatotopic organization of the gracile nucleus of the d
17                                          The somatotopic organization of the lateral striatum has bee
18 exact location of the neck motor area in the somatotopic organization of the motor homunculus is stil
19 rtially fits into the traditional concept of somatotopic organization of the nucleus.
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
25               To investigate conservation of somatotopic organization, we compared trigeminal nerve o
26                                   To examine somatotopic organization, we separately stimulated the l

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