ライフサイエンスコーパス: at rest

1 s that are mechanically strained over probes at rest.

2 heart rate (HR) were measured for 10 minutes at rest.

3 species are less likely to be attacked while at rest.

4 s in cerebellar connectivity were identified at rest.

5 as during a period of movement and a period at rest.

6 EEG and pupillometry during visual fixation at rest.

7 n, but similar pulmonary vascular resistance at rest.

8 EF were similar to those in control subjects at rest.

9 es to the maintenance of store Ca(2+) levels at rest.

10 creasing heights even if they were initially at rest.

11 s with pulmonary arterial hypertension (PAH) at rest.

12 human subjects measured non-invasively while at rest.

13 luding effects observed both during task and at rest.

14 patially constrained than local correlations at rest.

15 eus and the rest of the default mode network at rest.

16 exhibit spontaneous action potential firing at rest.

17 a temporally coordinated manner in task and at rest.

18 the visual cortex and sensory-motor networks at rest.

19 ory receptor cells maintain high sensitivity at rest.

20 , and she began to have dyspnea when she was at rest.

21 g exercise testing, with little relationship at rest.

22 emand during repetitive spike conduction and at rest.

23 from task-independent measurements collected at rest.

24 ves feels notably more slippery than it does at rest.

25 gic functional circuits in the healthy brain at rest.

26 background activity at disparate rates, even at rest.

27 lities and the increase of their alpha-power at rest.

28 obtained during stress by the value obtained at rest.

29 pacing has little, if any, variation in rate at rest.

30 uring electroencephalography recordings made at rest.

31 s are regulated by Ca(2+) signals that occur at rest.

32 ates were predictive of patterns of thinking at rest.

33 g V (m), and (2) when the dendritic V (m) is at rest.

34 s in the entire central nervous system (CNS) at rest.

35 cation of the strength of the microstructure-at-rest.

36 mplitude of compound muscle action potential at rest (0.21 mV), with a marked increase (700%; normal

37 /min/g; these were significantly higher than at rest (0.9 +/- 0.5 mL/min/g, P < 0.05) and were not di

38 whole-body DEE was approximately 150 kcal/d at rest (149 +/- 52 kcal/d), which decreased to approxim

39 D knockout (KO) mice also reduces Vo(2) both at rest (~15%) and during treadmill exercise (~12%).

40 levels, with reduced oxygen extraction both at rest (16.8% high affinity vs. 21.7% normal) and durin

41 oprusside, SNP), or potassium chloride (KCl) at rest; (2) mild or moderate intensity handgrip exercis

42 interval for pain score were higher for PCA at rest 24 hours postoperatively (0.59 [0.30, 0.88]), an

43 ents who could exercise and passed screening at rest, 31 (44%) had 1 vector safety, 16 (23%) had 2 ve

44 uction in pulmonary capillary wedge pressure at rest, 34 (58%) of 59 had a lower pulmonary capillary

45 reoperations (1.2% vs 0.9%; P = 0.019), pain at rest (5% vs 4.5%; P = 0.029), and on exertion (10.2%

46 reoperations (1.1% vs 0.8%; P = 0.008), pain at rest (5.2% vs 4.3%; P = 0.003), and pain on exertion

47 BQ-123 increased blood flow at rest (79 +/- 87 ml/min; P = 0.03) and augmented the e

48 BQ-123 reduced leg MAP at rest (-8 +/- 4 mmHg; P < 0.001) and lower intensities

49 form computer simulations of SVs near the PM at resting active zones, and the results show that the d

50 tening and lengthening of the macromolecules at resting active zones.

51 out (ATF3-KO) and control mice were analyzed at rest, after exercise, and after training.

52 er flow velocity measurements were performed at rest, after intracoronary adenosine, and during incre

53 At rest, although myocardial phosphocreatine/ATP was 14%

54 se in corticospinal excitability in subjects at rest; an increase was observed for both of the tested

55 n showed average relative differences of 10% at rest and 16% during exercise.

56 lity (grade A) TR Doppler was present in 68% at rest and 34% at peak exercise.

57 Thus, BK and Kv were mostly closed at rest and activated by depolarization.

58 c (10% O2) trial with measurements performed at rest and after 30 minutes of cycling at 70% of maxima

59 ish mice overexpressing UCP3 in muscle, both at rest and after exercise regimens that challenged musc

60 drin ((11)C-HED) and (15)O-water PET imaging at rest and after exposure to mild cold (16 degrees C) t

61 drin ((11)C-HED) and (15)O-water PET imaging at rest and after exposure to mild cold (16 degrees C) t

62 ower sympathetic activity and blood pressure at rest and any given physiological and environmental st

63 teriovenous anastomoses (IPAVAs) are present at rest and are recruited to a greater extent in conditi

64 Dynamic muscle ultrasonography at rest and at stress is often used for the diagnosis.

65 The pFRG is silent at rest and becomes rhythmically active during the stimu

66 fined as a margin-to-margin distance > 20 mm at rest and classified according to the following anatom

67 jugular venous blood samples were collected at rest and coupled with volumetric measures of cerebral

68 eatest for the legs, which surround the body at rest and create a diffuse transition from background

69 Imaging was performed at rest and during 6-min hypercapnic plateaus (baseline;

70 HF-HRV was assessed at rest and during a cognitive task protocol designed to

71 We also evaluated brain activity at rest and during a hippocampal-dependent pattern separ

72 p brain stimulation underwent functional MRI at rest and during a movement task; once with active dee

73 d frontostriatal reward system activity both at rest and during a sequential risky decision making ta

74 ces in left ventricular (LV) mechanics exist at rest and during acute physiological stress.

75 Cardiovascular physiology at rest and during acute stress (Montreal Imaging Stress

76 ine stress, and after contrast (0.2 mmol/kg) at rest and during adenosine stress, rendering rest and

77 (Ve), renal SNA (RSNA) and ECG were measured at rest and during CBC activation in sham and CHF rabbit

78 emission tomography assessing MVO(2) and MBF at rest and during dobutamine infusion.

79 assess phosphocreatine/ATP and CK kinetics, at rest and during dobutamine stress.

80 ry diameter and blood velocity were recorded at rest and during drug infusion.

81 istics of the electrocardiographic recording at rest and during exercise and genetic analyses.

82 effects of long-duration spaceflight on CBT at rest and during exercise are clearly lacking.

83 tients underwent right-heart catheterization at rest and during exercise at baseline and 12-week foll

84 levels of oxygen consumption can be achieved at rest and during exercise at the assumed cardiac outpu

85 ation with simultaneous expired gas analysis at rest and during exercise before and after treatment w

86 ve indexes of pulmonary artery (PA) function at rest and during exercise in HF patients without reduc

87 an IASD improves pulmonary vascular function at rest and during exercise in selected patients with HF

88 study compared indices of arterial stiffness at rest and during exercise in subjects with HFpEF and h

89 ization studies were prospectively conducted at rest and during exercise in subjects with invasively

90 concentration influences oxygen consumption at rest and during exercise via alterations in cardiac o

91 an age, 26 years +/- 1 [standard deviation]) at rest and during exercise with an MRI-compatible exerc

92 s the human cerebral and femoral circulation at rest and during exercise, an ideal model system chara

93 Skeletal muscle generates ROS at rest and during exercise.

94 accompanied by impaired coronary blood flow at rest and during exercise.

95 dentified that autonomic heat loss responses at rest and during fixed-intensity exercise in well-trai

96 Coronary pressure and flow were measured at rest and during hyperemia in both groups, before and

97 erfusion is lower in older individuals, both at rest and during incremental dynamic exercise.

98 Global myocardial blood flow was quantified at rest and during peak hyperemia.

99 ized pyruvate and magnetic resonance imaging at rest and during pharmacological stress, we investigat

100 g during HDT in healthy human subjects, both at rest and during recovery from leg-press exercises usi

101 aluation that includes repeated measurements at rest and during several provocative physiological cha

102 gional, and global left ventricular function at rest and during stress (exercise in 692, dipyridamole

103 lthy participants underwent echocardiography at rest and during submaximal exercise before completing

104 nd within (intracortical inhibition) the iS1 at rest and during tonic index finger voluntary activity

105 tion of BP via the Modified Oxford technique at rest and during VRCE.

106 Reduced pulmonary diffusing capacity at rest and excessively high ventilation during exercise

107 at exercise; n = 118), and C3 (E/e' >13 both at rest and exercise; n = 26) HF.

108 olic mitral annular velocity [E/e'] <13 both at rest and exercise; n = 63), C2 (E/e' >13 only at exer

109 ted by echocardiography and Doppler analysis at rest and following beta-adrenergic stimulation.

110 sea level (344 m) and high altitude (3800 m) at rest and following both maximal exercise and 30 min o

111 sea level (344 m) and high altitude (3800 m) at rest and following both maximal exercise and 30 min o

112 phalography scanning while participants were at rest and functional connectivity within networks was

113 relationships between ADSCT and both HF-HRV at rest and HF-HRV reactivity.

114 o, nitrite decreased aortic wave reflections at rest and improved arterial compliance and elastance a

115 erapies improve cardiac contractile function at rest and in response to adrenergic stimulation in obe

116 tomic, hemodynamic, and physiologic behavior at rest and in response to renal insults.

117 Cardiac performance was assessed at rest and in response to sympathomimetic challenge (do

118 f endogenous CD40L in unedited T cells, both at rest and in response to T-cell stimulation.

119 interact with higher cortical centres, both at rest and in the context of breathlessness threat.

120 d an attached, spread morphology in PMN both at rest and in the presence of chemotactic stimuli.

121 contributes to the control of blood pressure at rest and lower intensity exercise in these patients.

122 ary pressure and flow velocity were measured at rest and maximal hyperemia in undiseased vessels in 1

123 investigate the causes of screening failure at rest and on exercise to inform optimal S-ICD ECG vect

124 r sudden death underwent S-ICD ECG screening at rest and on exercise.

125 ractile units that were predominantly closed at rest and opened actively during muscle contractions i

126 e measurement of pulmonary arterial pressure at rest and peak exercise were simultaneously obtained.

127 years; 1.68 +/- 0.1 m(2) body surface area), at rest and post maximal incremental running.

128 phe nuclei led to excitation of tufted cells at rest and potentiation of their odor responses.

129 equency fluctuations in frontolimbic regions at rest and reduced fractional anisotropy in several whi

130 The increased connectivity at rest and reduced neural activation during task perfor

131 s (SGs) docked onto the plasma membrane (PM) at rest and reduced SG recruitment to the PM after gluco

132 span (20-89 years), we measured correlations at rest and related the functional connectivity patterns

133 Here, we analyze unit activity in humans at rest and show that spontaneous fluctuations in neural

134 oscillations in children (3-5 years; N = 65) at rest and tested our hypotheses that this temporal asy

135 t calsequestrin is polymerized within the SR at rest and that it depolymerized as [Ca(2+)] went down:

136 the topology of areal connectivity measured at rest and the functional recruitment of these areas du

137 of LE-PAD is the ankle-brachial index (ABI) at rest and typically an ABI </= 0.90 is used to define

138 ications for the test as well as vital signs at rest and under stress and the symptoms and adverse ef

139 domain composition in human oligodendrocytes at rest and under treatment with galactosylsphingosine (

140 ls with PTSD underwent functional MRI (fMRI) at rest and while completing three tasks assessing emoti

141 hout obstruction to left ventricular outflow at rest and/or under physiological exercise and to exami

142 e dependent heightened inflammatory profiled at resting and following LPS stimulation.

143 -free ratio, distal pressure/aortic pressure at rest, and FFR were measured in 763 patients from 12 c

144 ofrontal cortex/anterior insula was measured at rest, and its pattern of coupling with the other fron

145 egion, setting the fraction of channels open at rest, and possibly for the continued maintenance of s

146 ongestive heart failure, paraplegia, dyspnea at rest, and reoperation are associated with the highest

147 e-unit and multiunit data obtained in humans at rest, and show that firing rate covaries with CCD in

148 ains of BTN3A1 adopt a V-shaped conformation at rest, and that locking them in this resting conformat

149 n on F-actin, where it deters myosin binding at rest, and that, correspondingly, cross-bridge cycling

150 ies parallel to the horizon when the head is at rest, and used this assumption to reconstruct head po

151 ost muscle capillaries supporting blood flow at rest, and, rather than capillaries actively vasodilat

152 her relative amplitudes and longer durations at rest as well as during a cognitive task in epileptic

153 spectral resolution (31)P-MRS data, acquired at rest, as a marker of oxidative metabolism.

154 ivity within the cortico-basal ganglia loops at rest, as well as further modulations in the cortico-c

155 urn resulted in a high level of PNS activity at rest, as well as strong PNS activity withdrawal in re

156 at rest, stretched length and circumference at rest at 2, 6 and 12 months post-surgical procedure (a

157 d intensity for 20 min and TMS was performed at rest (before, during, and after tACS) and during move

158 riphosphate (ATP) and phosphocreatine levels at rest but cannot maintain normal ATP levels in the vis

159 ntion strengthens synapses that are inactive at rest but change their activity in anticipation of mov

160 mplex defence strategy; they are camouflaged at rest, but reveal a striking red-, blue-, and black-ba

161 onstrate that the brain's intrinsic coupling at rest can be selectively modulated by choosing appropr

162 aemoglobin concentration, oxygen consumption at rest can be sustained with the assumed cardiac output

163 ndings show that main MPH-related FC changes at rest can be understood through the distribution of DA

164 studies have shown that the valves are open at rest, can allow some backflow, and are a source of ni

165 graphy, collected from 104 patients measured at rest, can provide valuable information about brain co

166 At rest, compared with controls, patients with HFpEF had

167 with respect to how T1D affects spontaneous at-rest connectivity in young developing brains.

168 Here, we show that at rest cultured human effector memory and central memor

169 At rest, different lifetimes found for different organel

170 hort-latency intracortical inhibition (SICI) at rest during spontaneous high amplitude mu-alpha waves

171 VRCs were assessed at rest, during 30 min of induced limb ischaemia and dur

172 nd then remaining seated for 60 minutes also at rest, during recovery from the exercise.

173 in which the carotid bodies are hyperactive at rest, e.g. essential hypertension, obstructive sleep

174 g kg(-1) i.p.) would decrease cardiac output at rest (echocardiography), maximal aerobic capacity ( V

175 Using network analysis, we show that, at rest, eFC is consistent across datasets and reproduci

176 al hernias a significant higher rate of pain at rest [EHS I vs EHS II: odds ratio, OR = 1.350 (1.180-

177 BSTRACT: We examined the hypotheses that (1) at rest, endothelial function would be impaired at high

178 Our findings were: (1) at rest, FMD remained unchanged between sea level and hi

179 The groups endured 15 minutes seated at rest, followed by a submaximal aerobic exercise on a

180 placebo, the subjects were seated for 60 min at rest, followed by running on a treadmill at a submaxi

181 ps were acquired during adenosine stress and at rest following an intravenous contrast bolus (0.05 mm

182 nance imaging data from forty healthy humans at rest for the investigation of the basal scaffold of t

183 At rest, GLI slowed left ventricular relaxation (2.11 +/

184 blood pressure (DBP) and corresponding MSNA at rest (i.e. DBP 'operating pressure' and MSNA 'operati

185 that can be observed even when the brain is at rest, i.e. not engaged in any particular task.

186 C was 22 +/- 4 nl/min/mmHg at resting ICP and 13 +/- 3 nl/min/mmHg when ICP was rai

187 matic stress disorder that is in action even at rest, implicating dysregulated triangular sensory-pre

188 We investigated neuromagnetic brain activity at rest in 105 participants divided into three age group

189 sterone alter functional cerebellar networks at rest in a woman densely sampled over a complete menst

190 ricular outflow tract obstruction is present at rest in about one third of the patients and can be pr

191 at could explain the functional MRI activity at rest in an attempt to reproduce and extend the findin

192 We measured choline at rest in both the dorsal and ventral striatum using ma

193 thology and the basal forebrain connectivity at rest in cognitively intact older adults at risk for A

194 The similarity of HFOs properties recorded at rest in epileptic and non-epileptic hippocampi sugges

195 moglobin formation (venous>arterial; P<0.05) at rest in normoxia, during hypoxia (P<0.05 versus normo

196 BK/Kv were mostly closed at rest in normoxia.

197 ng did not extend to functional connectivity at rest in our population.

198 between OP1/OP4 functional connectivity (FC) at rest in stroke versus healthy adults to then explore

199 spectroscopy, we showed that choline levels at rest in the dorsal striatum are associated with perfo

200 nts show abnormalities in brain connectivity at rest, including hyperconnectivity within the default

201 of this network is present in brain activity at rest, independently of any stimulus and of any paroxy

202 heart failure, daytime oscillatory breathing at rest is associated with a high risk of mortality.

203 cal network generating the alpha oscillation at rest is different in people with epilepsy and visual

204 Cerebral functional connectivity at rest is lower in ADHD patients when compared with hea

205 Mobility at rest is regulated by alternative splicing of the flip

206 either sex) evoked by steady depolarization at rest is replaced by irregular firing during functiona

207 An impaired decline in blood pressure at rest is typical in people with diabetes, reflects end

208 red with previous work, the fluid was almost at rest, leading to fewer, straighter, and slower-moving

209 Loading leg muscles during HDT at rest led to significantly higher values of arterial b

210 o be important in top-down executive control at rest (left dlPFC), which, in turn, is associated with

211 SS (Kcnj16-/-) rats hyperventilated at rest, likely compensating for a chronic metabolic aci

212 We evaluated left ventricular function at rest, maximal aerobic capacity ( V O(2) max) and subm

213 l stimulation rather than their organisation at rest may be primarily disturbed in IBS.

214 T2 MRI at adenosine stress was greater than at rest (mean rest vs stress, 38.7 msec +/- 2.5 [standar

215 yperpolarized voltages and increased I (NaP) at resting membrane potential.

216 sis' that rundown of inhibitory SK responses at resting membrane potentials (RMPs) reflects depletion

217 ellular calcium stores, and run down rapidly at resting membrane potentials when calcium stores becom

218 In contrast, when the dendritic V (m) is at rest, mGluR1s increase dendritic excitability by inac

219 d heart rate variability (HRV) were measured at rest, midpoint of the session, immediately after the

220 ge 53+/-8 years, 63% women) with blood drawn at rest (n=471) and at peak exercise (n=411).

221 rt failure, paraplegia, reoperation, dyspnea at rest, nongastric band surgery, age >/=60 years, male

222 t differ between sea level and high altitude at rest, nor following maximal exercise.

223 2 , capnography) were performed during 5 min at rest (normocapnia) and during four breathing manoeuvr

224 nd heart rate (ECG) were performed for 5 min at rest (normocapnia) and during hypercapnia induced by

225 Functional MRI scans acquired at rest offer insights into functional integration via p

226 e demonstrate that hydrogel drops, initially at rest on a surface, spontaneously jump upon rapid heat

227 e acquired in supine position in the morning at rest once before the expedition (baseline) and monthl

228 r without a 5 wk endurance training protocol at rest or after an acute exercise bout (EB).

229 ding on whether the antibody uptake occurred at rest or during depolarization.

230 There was no reduction in Qs following IASD at rest or during exercise.

231 An animal at rest or engaged in stationary behaviors can instantan

232 ficant improvement in neither CI nor PCWP/CI at rest or exercise.

233 nally moved target (while keeping their hand at rest or not).

234 tacts is central to this effect-for mixtures at rest or shearing slowly, repulsion prevents frictiona

235 ffectiveness was defined as changes in pain (at rest or with activity) greater than 13 mm on a 100-mm

236 with a 2-week history of shortness of breath at rest, orthopnea, and lower extremity edema.

237 bility and GABA concentrations were measured at rest, outside a task context, providing assays of int

238 CV, and MBV at stress, and perfusion and ECV at rest (p < 0.01 for all).

239 to evoked PVCs (p = 0.005), heart rate (HR) at rest (p = 0.003), and exercise (p < 0.04) increased,

240 trol diet were determined to spend more time at rest (p = 0.053).

241 tients (<55 y) revealed higher rates of pain at rest, pain on exertion, and pain requiring treatment

242 near the mid-point of the adjustment ranges at resting PaO2 where sensitivity is maximum.

243 At rest, patients with mitochondrial disease exhibit ele

244 At rest, PCWP was <12 mm Hg in 11 patients (44%) with LA

245 At rest, perfusion and T(2)* in gastrocnemius muscle gro

246 imens were collected at three time intervals at rest, postexercise, and recovery.

247 At resting potential (-63.7 +/- 0.6 mV), approximately 9

248 k coupling through spontaneous alpha rhythms at rest predict performance.

249 measured pulmonary capillary wedge pressure at rest (r=0.63, P<0.0001) and during exercise (r=0.57,

250 ed reasonably well with invasive measurement at rest (r=0.72, P<0.001; bias, -2.9+/-8.0 mm Hg) and pe

251 Hippocampal fMRI patterns recorded at rest reflected sequentiality of previously experience

252 nectional topology of brain areas quantified at rest relates to the functional activity of those area

253 Platelets lacking Slc44a2 contain less ATP at rest, release less ATP when activated, and have an ac

254 maximal sensitivity, tip links are tensioned at rest, resulting in a continuous influx of Ca(2+) into

255 As compared to pulmonary vascular resistance at rest, slope of increase in pulmonary pressure relativ

256 owing evidence has shown that brain activity at rest slowly wanders through a repertoire of different

257 impaired evoked release, whereas HRP uptake at rest solely potentiated spontaneous release.

258 Our brains at rest spontaneously replay recently acquired informati

259 here were no group differences in uOR BP(ND) at resting state (early phase).

260 frequency, [Na(+)]sm is bounded between 9 mM at resting state and 11.5 mM; and 3) the cells can maint

261 y is shown to enhance mPFC/ACC activity even at resting state and improve cognitive function in patie

262 isolated from the ethanol and control groups at resting state within each major gut section, our anal

263 R nondisplaceable binding potential (BP(ND)) at resting state, and the last 45 min consisted of a 20-

264 ion, as well as glucose and lipid metabolism at resting state, even when fed a high-fat diet.

265 Immunocytochemical staining revealed that, at resting state, p47phox colocalizes with NOX2, whereas

266 er working state and functional connectivity at resting state.

267 the mid-valent iron centres of FeMo cofactor at resting state.

268 me (SV) acetylene rebreathing) were examined at rest, steady-state submaximal exercise and maximal ex

269 We found a significant improvement in length at rest, stretched length and circumference at rest at 2

270 Fusion pore opening at resting synapses provides a mechanism for activity-in

271 g (phase lag index) that was more widespread at rest than during walking.

272 At rest the lPAG was functionally correlated with cortic

273 For terminals fixed at rest, the contact area between the VM of docked vesic

274 stimuli and to delineate functional circuits at rest, the extent to which BOLD signals correlate spat

275 face-processing network were tightly coupled at rest, the strength of these connections did not predi

276 Initially at rest, these self-propelled drops accelerate within a

277 is that they can transform from liquid-like at rest to solid-like under sudden impact.

278 ons between two relatively indistinct states at rest, toward a sequence of well-defined functional st

279 Data were obtained at rest, two submaximal levels of exercise below ventila

280 Echocardiography was performed at rest, under anesthesia.

281 volume (SV) during voluntary surface apneas at rest up to 255 s, and during recovery from apnea in 1

282 lls and bone marrow-derived basophils (BMBs) at rest, upon an adaptive-type activation (IgE cross-lin

283 erindividual variability in dopamine release at rest using [(11)C]raclopride positron emission tomogr

284 oxygen consumption as a fraction of delivery at rest ( VO2 = 0.25 L min(-1) , cardiac output = 5.70 L

285 Pulmonary diffusing capacity at rest was a significant predictor of dead space ventil

286 Median MBF at rest was comparable between CZT and PET (0.89 [interq

287 CBF at rest was quantified on a voxelwise basis using arteri

288 Higher HF-HRV at rest was significantly related to both more severe AD

289 ther neural homophily between friends exists at rest we collected resting-state functional magnetic r

290 While mitral cells at rest were also excited by raphe activation, their odo

291 Neuropathy and skin blood flow at rest were assessed in response to acetylcholine, sodi

292 rger motor-evoked potentials (MEPs) measured at rest were associated with faster RTs.

293 between practice periods, when subjects were at rest, were significant and accounted for early proced

294 o systematically interrogate these disorders at rest, when muscle symptoms are typically minimal, and

295 t in the lumen of the sarcoplasmic reticulum at rest, whereas Ca(2+) concentrations similar to those

296 patients with ME/CFS had reduced glycolysis at rest, whereas CD8+ T cells also had reduced glycolysi

297 The vlPAG showed fronto-limbic correlations at rest, whereas during breathlessness anticipation, red

298 en frontoparietal and limbic brain circuitry at rest, which may reflect a potential mechanism or bios

299 oxygenation level-dependent signals measured at rest with functional magnetic resonance imaging.

300 We measured corticospinal excitability at rest with transcranial magnetic stimulation, local co