1 as an experimental model to induce local and referred pain.

2  noxious punctate stimulus in their areas of referred pain.

3 ative sensory testing (QST) in their area of referred pain.

4 hritis (OA) is often accompanied by areas of referred pain and changes in skin sensitivity.

5  at the frontal aspect of the ankle (area of referred pain) and on the arm.

6 sure stimuli applied to the local pain area, referred pain area and an arm was assessed in 14 healthy

7 n deep sensibility at the heterotopic sites (referred pain area and arm), but not at homotopic sites

8  allodynia occurred either solely within the referred pain area on the ipsilateral head, or within an

9 in response to punctate stimulation of their referred pain areas compared with healthy controls, and

10 r associated with stimulation of the skin in referred pain areas of patients with hip OA.

11 s for peak pain time points and evidence for referred pain assessment when studying soft tissue augme

12 ting in persistent visceral hyperalgesia and referred pain in rats, modeling some aspects of postinfl

13        An exaggerated visceromotor response, referred pain to mechanical stimulation, increased spina

14 ng joint replacement and displaying signs of referred pain were recruited into the study, together wi

15 c resonance imaging (MRI) while the areas of referred pain were stimulated using cold stimuli (12 deg