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1 ither baseline cardiovascular parameters nor baroreflex sensitivity.
2 ence between control and occlusion groups in baroreflex sensitivity.
3 ied Oxford technique to assess cardiac vagal baroreflex sensitivity.
4 in an increase in HRV and an improvement in baroreflex sensitivity.
5 ivity and negatively correlated with cardiac baroreflex sensitivity.
6 heart, leading to hypertension and depressed baroreflex sensitivity.
7 vs. sham-operated SHR) and an improvement in baroreflex sensitivity.
8 trual cycle had no influences on cardiovagal baroreflex sensitivity.
9 ssed according to heart rate variability and baroreflex sensitivity.
10 renal sympathetic nerve activity and to test baroreflex sensitivity.
11 an increase in parasympathetic activity and baroreflex sensitivity.
12 ors with a possible reduction in sympathetic baroreflex sensitivity.
13 ood pressure and a smaller change in cardiac baroreflex sensitivity.
14 ivity to higher pressures without changes in baroreflex sensitivity.
15 , employing heart rate variability (HRV) and baroreflex sensitivity.
16 ympathetic nerve activity without changes in baroreflex sensitivity.
17 r the Fontan operation, with reduced HRV and baroreflex sensitivity.
18 transdermal nor oral ERT had any effects on baroreflex sensitivity.
19 d more impaired autonomic balance, ie, lower baroreflex sensitivity (1.4 +/- 1.3 versus 5.0 +/- 1.5 m
20 hostatic intolerance had lower cardiac vagal baroreflex sensitivity (12+/-1 versus 25+/-4 ms/mm Hg; P
21 antecedent hypoglycemia leads to 1) reduced baroreflex sensitivity (16.7 +/- 1.8 vs. 13.8 +/- 1.4 ms
24 cal responsiveness to ACTH, but had enhanced baroreflex sensitivity and augmented plasma catecholamin
26 ostatic intolerance have lower cardiac vagal baroreflex sensitivity and marginally lower blood volume
28 goal was to test sympathetic and cardiovagal baroreflex sensitivity and the transduction of sympathet
29 ngiotensin II levels, inflammation, impaired baroreflex sensitivity, and autonomic dysfunction, as we
31 ormalized indexes of sympathetic outflow and baroreflex sensitivity, and reduced the incidence of apn
32 c nervous system--heart rate variability and baroreflex sensitivity--are reviewed, and the clinical a
35 m, mean and maximum (+/-s.d.) supine control baroreflex sensitivities averaged 5 +/- 3, 18 +/- 6, and
36 fferences in the cardiovagal and sympathetic baroreflex sensitivities between phases under any condit
38 alysis of heart rate variability [HRV]), and baroreflex sensitivity (bolus phenylephrine method and a
39 systolic blood pressure, cardiac parameters, baroreflex sensitivity (BRS) and hyperinsulinemia in the
40 Although heart rate variability (HRV) and baroreflex sensitivity (BRS) are recognized as independe
43 lex function as indicated by the blunting of baroreflex sensitivity (BRS) following the antagonizatio
47 ter standard tests of autonomic function and baroreflex sensitivity (BRS) measurement, diabetic parti
51 bute to sympathetic overactivity, attenuated baroreflex sensitivity (BRS), and excessive ventilation
52 ventilatory recruitment threshold (VRT-CO2), baroreflex sensitivity (BRS), blood pressure, and blood
55 ailure (CHF) results in blunting of arterial baroreflex sensitivity (BRS), which arises from alterati
59 od pressure or heart rate, or to cardiovagal baroreflex sensitivity, but correlated with muscle sympa
60 /DeltaMAP, which does not involve changes in baroreflex sensitivity, but may involve changes in chemo
61 nism for the decrease in spontaneous cardiac baroreflex sensitivity (cBRS) during exercise in humans.
63 at 0.6 of gestation; however, fetal cardiac baroreflex sensitivity decreased with advancing gestatio
64 ared with baseline euglycemic conditions, 1) baroreflex sensitivity decreases significantly (19.2 +/-
66 d pressure and baroreflex threshold, reduced baroreflex sensitivity, diminished plasma catecholamine
68 athetic neural responses but not sympathetic baroreflex sensitivity during orthostasis, though uprigh
69 x sensitivity with OC differ from changes in baroreflex sensitivity during the normal menstrual cycle
71 sibly 'steady-state' conditions, human vagal baroreflex sensitivity fluctuates in a major way, at ver
72 t during brief periods of observation, human baroreflex sensitivity fluctuates widely and rhythmicall
76 ween arrhythmic events and predictive tests (baroreflex sensitivity, heart rate turbulence, heart rat
78 mpathetic nerve activity and reduced cardiac baroreflex sensitivity heighten cardiovascular risk, alt
80 er, intravenous CV-11974 failed to alter the baroreflex sensitivities in area postrema-lesioned SHRs.
83 y 5959 affects the control of heart rate and baroreflex sensitivity in conscious dogs with pacing-ind
85 hough studies have examined resting arterial baroreflex sensitivity in older subjects, little attenti
86 mpathetic nerve activity and reduced cardiac baroreflex sensitivity in patients with RA compared to m
87 of ANA-12 into the dmNTS greatly diminished baroreflex sensitivity in sham rats, whereas it had less
89 s measurements of heart rate variability and baroreflex sensitivity in the neuromonitoring setting of
92 upled with impairments in renal function and baroreflex sensitivity, increased neuroinflammatory mark
94 eart rate variability, endothelial function, baroreflex sensitivity, inflammation, and platelet funct
96 Not only sympathetic but also cardiovagal baroreflex sensitivity is similar between sexes and mens
97 t, as measured by heart rate variability and baroreflex sensitivity, is significantly associated with
98 ns of physiological abnormalities: depressed baroreflex sensitivity low LF/HF low LF/(HF + LF) low al
101 function, including decreased cardiac vagal baroreflex sensitivity, may contribute directly to morta
102 ing age, left ventricular ejection fraction, baroreflex sensitivity, mean RR interval, standard devia
103 thetic nerve activity (MSNA) and sympathetic baroreflex sensitivity (MSNA-diastolic pressure relation
104 ivity (n=38), heart rate variability (n=34), baroreflex sensitivity (n=20), and ergoreflex activity (
107 No significant differences in cardiovagal baroreflex sensitivity or vascular transduction were obs
108 ent of heart rate variability (P<0.0001) and baroreflex sensitivity (P=0.03), and overactive ergorece
109 , it still decreased heart rate and restored baroreflex sensitivity (PI/SAP slope, 12.7+/-2.8 ms/mm H
110 central chemoreceptor sensitivity, arterial baroreflex sensitivity, plasma norepinephrine, epinephri
114 emetry), autonomic function, and spontaneous baroreflex sensitivity (SBRS) were not significantly dif
131 s measurements of heart rate variability and baroreflex sensitivity we aimed to test whether autonomi
133 y-four-hour ambulatory BP, SND, and arterial baroreflex sensitivity were measured before and after 8
134 t subjects, moderate ongoing fluctuations of baroreflex sensitivity were punctuated by brief major pe
138 art rate variability, heart rate turbulence, baroreflex sensitivity) were significant predictors of a
139 stiffness; (2) it is associated with reduced baroreflex sensitivity, which increases blood pressure v
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