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1                                              TENS facilitated urinary continence recovery after VD.
2                                              TENS inhibits IL-1beta-induced synthesis of IL-1beta, IL
3                                              TENS or SH-TENS were applied immediately and at days 2 a
4                                              TENS reduces hyperalgesia through activation of receptor
5                                              TENS significantly decreased the frequency of urine leak
6                                              TENS-L is a potent inhibitor of interleukin (IL)-1 beta-
7 ontrol groups, who were not influenced about TENS.
8 extracellular fluid before, during and after TENS and analyzed GABA in dialysates with high performan
9 tic machines, and more recently with TMS and TENS.
10 ory and proinflammatory signals generated by TENS of various magnitudes.
11 rs prevents the antihyperalgesia produced by TENS in rats with joint inflammation.
12                                 In contrast, TENS-H is a proinflammatory signal that induces I-kappaB
13                                        Daily TENS therapy showed potential in reducing functional int
14 4-h VD, 4-h sham VD (SH-VD), VD plus 1-h DNC TENS, and VD plus 1-h sham TENS (SH-TENS).
15 gia diagnostic criteria undergoing high-dose TENS showed GFI improvement at 4-weeks from baseline (me
16                  We show that high frequency TENS increases extracellular GABA concentrations in the
17                         Thus, high frequency TENS increases release of GABA in the deep dorsal horn o
18 glycine in response to low or high frequency TENS.
19 hypothesis that either high or low frequency TENS applied to the inflamed knee joint increases GABA i
20  hyperalgesia by both high and low frequency TENS is prevented by spinal blockade of GABA(A) receptor
21 spinal cord, and both high and low frequency TENS reduce primary hyperalgesia by activation of GABA(A
22 BA do not occur in response to low frequency TENS, and there are no increases in glycine in response
23 dditional studies are necessary to assess if TENS could be used in postpartum women.
24 y, whereas tensile strain of high magnitude (TENS-H) is proinflammatory and catabolic.
25 equibiaxial tensile strain of low magnitude (TENS) provokes potent anti-inflammatory signals in PDL c
26 enerated by tensile strain of low magnitude (TENS-L) are antiinflammatory, whereas tensile strain of
27 l group was conditioned about the effects of TENS with a surreptitious amplification of the visual fe
28          Both groups received daily 3-5 h of TENS therapy for 4-weeks.
29 our therapeutic modalities (sham-PENS, PENS, TENS, and exercise therapies) were each administered for
30  scores after each treatment than sham-PENS, TENS, and exercise therapies (after-treatment mean +/- S
31  and 2.6+/-1.2 pills per day with sham-PENS, TENS, and exercise, respectively.
32  posttreatment function more than sham-PENS, TENS, and exercise.
33 n group, IG) or low dose (placebo group, PG) TENS device.
34                                   TENS or SH-TENS were applied immediately and at days 2 and 4 post-V
35  1-h DNC TENS, and VD plus 1-h sham TENS (SH-TENS).
36 , VD plus 1-h DNC TENS, and VD plus 1-h sham TENS (SH-TENS).
37 dditionally, as an anti-inflammatory signal, TENS induces IL-10 synthesis in the presence and absence
38  The most common reported etiologies for SJS/TENS were antibiotics (n = 25), ibuprofen (n = 15), and
39 5 males and 51 females with a history of SJS/TENS; median age was 36 years.
40 ss if transcutaneous electrical stimulation (TENS) of the dorsal nerve of the clitoris facilitates re
41 transcutaneous electrical nerve stimulation (TENS) and anodal transcutaneous spinal direct current st
42 transcutaneous electrical nerve stimulation (TENS) applied on the first dorsal interosseus would indu
43 Transcutaneous Electrical Nerve Stimulation (TENS) for fibromyalgia-like symptoms including chronic w
44 Transcutaneous electrical nerve stimulation (TENS) is a commonly utilized non-pharmacological, non-in
45 limb using transcutaneous nerve stimulation (TENS).
46 ntrolled study, PENS was more effective than TENS or exercise therapy in providing short-term pain re
47 eached higher levels of force, believed that TENS had been effective and expected to perform better c
48 servations are the first to demonstrate that TENS antagonizes IL-1beta actions on PDL cells by (i) in
49                                 We show that TENS performed before a bout of WPHF NMES results in low
50 tra torque can be modulated and although the TENS intervention blunted extra torque production, the f