ライフサイエンスコーパス: thenar

1 bilateral (simultaneous) stimulation of both thenars.

2 0 microV, 41, 0-129 vs 96 microV, 0, 0-195); thenar (259 microV, 258, 0-538 vs 451 microV, 206, 8-717

3 V, 239, 89-372 vs 239 microV, 163, 133-307), thenar (572 microV, 463, 175-638 vs 638 microV, 485, 381

4 populations of motor neurons innervating the thenar and first dorsal interosseous muscles during task

5 populations of motor neurons innervating the thenar and first dorsal interosseous muscles in humans d

6 adolescent onset of weakness, and atrophy of thenar and first dorsal interosseus muscles progressing

7 ement sites: cerebral, deltoid, forearm, and thenar) and finger photoplethysmographic perfusion index

8 turnal paresthesias; Phalen and Tinel signs; thenar atrophy; and 2-point, vibratory, and monofilament

9 Pharyngeal and thenar electromyographic responses to magnetic stimulati

10 yngeal dysphagia, mylohyoid, pharyngeal, and thenar electromyographic responses to stimulation of aff

11 Thenar eminence and brain tissue oxygenation and side-st

12 the highest mean rSO(2) (~ 75.8%), while the thenar eminence and forehead showed the lowest.

13 We measured oxygen consumption in the thenar eminence during brachial artery occlusion in sick

14 were delivered to a central location on the thenar eminence of the hand.

15 r") stimulation applied independently to the thenar eminence on each hand and also to bilateral (simu

16 Nonpainful punctate stimulation of the thenar eminence provoked more diffuse activity but was s

17 hemodynamic variables and also cerebral and thenar eminence tissue oxygenation and side-stream dark-

18 ets shown to innervate the middle finger and thenar eminence were also transected.

19 modulatory influences evoked by ipsilateral thenar flutter stimulation reach SI via a two-stage path

20 b accompanied by the strong adduction of the thenar, hypothenar, and palmar interosseous muscles offe

21 ecorded every other hour at the level of the thenar, masseter, and deltoid muscles along with central

22 y change the contractile properties of human thenar motor units more than paralysis alone.

23 Our aim was to determine the fatigability of thenar motor units paralysed chronically (10 +/- 2 years

24 aneural stimulation of single motor axons to thenar motor units.

25 r-infrared resonance spectroscopy to measure thenar muscle microvascular function (StO(2)recov) and o

26 Pull-down was not observed in the thenar muscle responses to median nerve stimulation in a

27 On average, 75% of the motor units for the thenar muscles and first dorsal interosseus were strongl

28 The SWV measurements of the skin and the thenar muscles were also affected by transducer compress

29 The skin and the thenar muscles were also examined as reference tissues.

30 and it had a particular predilection for the thenar muscles.

31 mulation (TMS) to co-localise pharyngeal and thenar representation in the cortex and cerebellum (midl

32 In contrast, thenar representation increased in the affected hemisphe

33 phagic patients showed similar mylohyoid and thenar responses to stimulation of the unaffected hemisp

34 wo hand muscles (first dorsal interossei and thenars, seven men and one woman) during submaximal isom

35 Thenar StO2 (HT) showed no statistical change throughout

36 measurement device (UMMS) and compared with thenar StO2 measured by a commercial device (HT).

37 rea under the curve 0.88; 0.77-0.98) but not thenar tissue oxygen saturation (area under the curve 0.

38 f central venous oxygen saturation >70% than thenar tissue oxygen saturation (area under the curve, 0

39 but not central venous oxygen saturation or thenar tissue oxygen saturation are strong predictors of

40 Over the 6-hr resuscitation period, thenar tissue oxygen saturation was consistently higher

41 t occur subsequent to a 15-s exposure of the thenar to 25 Hz or 200 Hz stimulation are proposed to re

42 he range of fatigability typically found for thenar units, only its magnitude.