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1 ences of SNA bursts and non-bursts (peroneal microneurography).
2 rodes in nerves and thus has advantages over microneurography.
3 etic nerve activity (MSNA) was determined by microneurography.
4 thetic nerve activity (MSNA) was measured by microneurography.
5 ied clinically and thermographically, and by microneurography.
6 e sympathetic nerve activity was recorded by microneurography.
7 iscrete stimulus-response properties through microneurography.
8 ning their response to hair deflection using microneurography.
9 zed 36 consecutive long COVID patients using microneurography.
10 e), muscle sympathetic nerve activity (MSNA; microneurography, 12 paired recordings), and beat-to-bea
11             MSNA was measured using peroneal microneurography and BRS was measured using the spontane
12                                        MSNA (microneurography) and blood pressure (BP; photoplethysmo
13 pathetic nerve activity (MSNA; determined by microneurography) and diastolic blood pressure.
14 lating muscle sympathetic nerve activity (by microneurography) and diastolic blood pressure.
15                               SSNA (peroneal microneurography) and red cell flux (laser Doppler flowm
16                               SSNA (peroneal microneurography) and red cell flux (laser-Doppler flowm
17                In Protocol 1, SSNA (peroneal microneurography) and red cell flux in the affected derm
18  cocaine-naive humans, we measured skin SNA (microneurography) and skin blood flow (laser Doppler vel
19 by venous occlusion plethysmography, MSNA by microneurography, and blood pressure by beat-to-beat non
20 n human participants, using the technique of microneurography, and stimulated a unit's receptive fiel
21 lectrophysiological characterization through microneurography, and the correlation with pain percepts
22 tivity was measured in the peroneal nerve by microneurography, and the slope of the relations between
23 ts suggest that alternative measures such as microneurography are required to understand the relation
24                       In 19 young men, MSNA (microneurography), arterial blood pressure and brachial
25 athetic activity by measuring MSNA (peroneal microneurography), arterial pressure (arterial catheter)
26     We measured multifibre muscle SNA (MSNA; microneurography), arterial pressure (brachial catheter)
27                   We measured MSNA (peroneal microneurography), arterial pressure (brachial line), CO
28                         MSNA was measured by microneurography at the peroneal nerve, and arterial blo
29 red muscle sympathetic nerve activity (MSNA; microneurography), beat-to-beat BP (photoplethysmography
30                                        MSNA (microneurography), body composition (dual energy x-ray a
31                                              Microneurography confirmed discordant sympathetic activa
32 d model with a neural dynamic model by using microneurography data to predict neural responses based
33 asured heart rate, blood pressure, and MSNA (microneurography) during (1) 7-minute baseline; (2) 2-mi
34 ation and muscle sympathetic nerve activity (microneurography) during 3 min of underlying basal heart
35 NA action potential (AP) discharge patterns (microneurography) during incremental rhythmic handgrip e
36 ppler flowmetry), local sweat rate and SSNA (microneurography from peroneal nerve).
37                            We assessed SSNA (microneurography) from the peroneal nerve and skin blood
38 yperactivity in hypertension with the use of microneurography have been inconsistent.
39 e afferent responses from alert humans using microneurography, I show that spindle output does reflec
40                                              Microneurography identified 13 primary cutaneous C-nocic
41 echnically challenging approaches, including microneurography in humans and teased fibre electrophysi
42 ting the dorsum of the foot were recorded by microneurography in seven healthy volunteers.
43 was measured during wakefulness via peroneal microneurography in seven patients with documented OSA b
44 double conditioning impulses were studied by microneurography in single human C fibres to provide inf
45 mpulse-dependent velocity changes by in vivo microneurography in the rat sciatic nerve.
46 e sympathetic nerve activity (MSNA, peroneal microneurography) in 5 healthy humans under conditions o
47 and muscle sympathetic nerve activity (MSNA, microneurography) in eight patients with sleep apnea and
48 entials, contact heat-related potentials and microneurography may reveal the extent of damage to smal
49 = 16) and muscle sympathetic nerve activity (microneurography; n = 11) was assessed in healthy men an
50    Six additional control patients underwent microneurography of the peroneal nerve to compare the sy
51                            We measured MSNA (microneurography of the peroneal nerve) and forearm bloo
52                                        MSNA (microneurography of the peroneal nerve), continuous arte
53 actions occurred in 21 patients, including 7 microneurography patients.
54 n punch biopsy, corneal confocal microscopy, microneurography, quantitative sensory testing including
55                   Molecular-profile-informed microneurography recordings revealed temperature-sensing
56 sed muscle sympathetic nerve activity (MSNA, microneurography) responsiveness to the Trier social str
57                              Skin biopsy and microneurography revealed an absence of C-fiber nocicept
58                                              Microneurography revealed initial activity-dependent acc
59 tly blocked C-fiber nociceptor conduction in microneurography studies and inhibited withdrawal respon
60 ry pressure (PAP) above normal, whilst MSNA (microneurography), systemic blood pressure (photoplethys
61   Single unit activity was recorded with the microneurography technique from sixteen spindle afferent
62                              This study used microneurography to assess the effects of ischaemia on s
63 uscle sympathetic nerve activity (MSNA)] via microneurography was recorded at rest and during stress
64                                              Microneurography was used to record C nociceptors of 30
65  Muscle sympathetic nerve activity (peroneal microneurography) was 74% higher in the older men (P<0.0
66                                        Using microneurography, we simultaneously recorded the activit
67  of the arterial baroreceptors, and MSNA via microneurography were continuously recorded to determine
68 , heart rate (electrocardiography) and MSNA (microneurography) were assessed at the initial and final
69 sure, and muscle sympathetic nerve activity (microneurography) were monitored at baseline and up to 2
70 emodynamics (photoplethysmography) and MSNA (microneurography) were recorded lying supine.
71 le sympathetic nerve activity (MSNA, fibular microneurography) when clamping end-tidal gases at basel
72  muscle sympathetic nerve activity (MSNA) by microneurography, whole-body norepinephrine kinetics by