ライフサイエンスコーパス: microneurography

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1 etic nerve activity (MSNA) was determined by microneurography.

2 thetic nerve activity (MSNA) was measured by microneurography.

3 ied clinically and thermographically, and by microneurography.

4 e sympathetic nerve activity was recorded by microneurography.

5 iscrete stimulus-response properties through microneurography.

6 MSNA was measured using peroneal microneurography and BRS was measured using the spontane

7 pathetic nerve activity (MSNA; determined by microneurography) and diastolic blood pressure.

8 lating muscle sympathetic nerve activity (by microneurography) and diastolic blood pressure.

9 SSNA (peroneal microneurography) and red cell flux (laser Doppler flowm

10 In Protocol 1, SSNA (peroneal microneurography) and red cell flux in the affected derm

11 cocaine-naive humans, we measured skin SNA (microneurography) and skin blood flow (laser Doppler vel

12 by venous occlusion plethysmography, MSNA by microneurography, and blood pressure by beat-to-beat non

13 n human participants, using the technique of microneurography, and stimulated a unit's receptive fiel

14 tivity was measured in the peroneal nerve by microneurography, and the slope of the relations between

15 In 19 young men, MSNA (microneurography), arterial blood pressure and brachial

16 athetic activity by measuring MSNA (peroneal microneurography), arterial pressure (arterial catheter)

17 We measured multifibre muscle SNA (MSNA; microneurography), arterial pressure (brachial catheter)

18 We measured MSNA (peroneal microneurography), arterial pressure (brachial line), CO

19 MSNA was measured by microneurography at the peroneal nerve, and arterial blo

20 MSNA (microneurography), body composition (dual energy x-ray a

21 Microneurography confirmed discordant sympathetic activa

22 ation and muscle sympathetic nerve activity (microneurography) during 3 min of underlying basal heart

23 ppler flowmetry), local sweat rate and SSNA (microneurography from peroneal nerve).

24 We assessed SSNA (microneurography) from the peroneal nerve and skin blood

25 yperactivity in hypertension with the use of microneurography have been inconsistent.

26 e afferent responses from alert humans using microneurography, I show that spindle output does reflec

27 Microneurography identified 13 primary cutaneous C-nocic

28 ting the dorsum of the foot were recorded by microneurography in seven healthy volunteers.

29 was measured during wakefulness via peroneal microneurography in seven patients with documented OSA b

30 double conditioning impulses were studied by microneurography in single human C fibres to provide inf

31 mpulse-dependent velocity changes by in vivo microneurography in the rat sciatic nerve.

32 e sympathetic nerve activity (MSNA, peroneal microneurography) in 5 healthy humans under conditions o

33 and muscle sympathetic nerve activity (MSNA, microneurography) in eight patients with sleep apnea and

34 = 16) and muscle sympathetic nerve activity (microneurography; n = 11) was assessed in healthy men an

35 Six additional control patients underwent microneurography of the peroneal nerve to compare the sy

36 We measured MSNA (microneurography of the peroneal nerve) and forearm bloo

37 actions occurred in 21 patients, including 7 microneurography patients.

38 Single unit activity was recorded with the microneurography technique from sixteen spindle afferent

39 This study used microneurography to assess the effects of ischaemia on s

40 Microneurography was used to record C nociceptors of 30

41 Muscle sympathetic nerve activity (peroneal microneurography) was 74% higher in the older men (P<0.0

42 of the arterial baroreceptors, and MSNA via microneurography were continuously recorded to determine

43 sure, and muscle sympathetic nerve activity (microneurography) were monitored at baseline and up to 2

44 muscle sympathetic nerve activity (MSNA) by microneurography, whole-body norepinephrine kinetics by

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