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1 ivation and amplitude of release varied from beat to beat.
2 Ca(2+) release from these sites varied from beat to beat.
3 ts indicating a change in contractility from beat to beat.
4 s occur with durations varying randomly from beat to beat.
8 rm for addressing heart disease and enabling beat-to-beat adaptation of cardiac pacing in response to
10 ng, and were not merely passive responses to beat-to-beat alterations in AP; 3) the complex Ca(2+) dy
11 t modulation of stroke volume (SV) caused by beat-to-beat alterations in left ventricular filling, wh
14 own that small depolarizing pulses produce a beat to beat alternation in the amplitude of the systoli
17 tive trigger event for cardiac reentry, is a beat-to-beat alternation in membrane potential and calci
19 heart, in which rapid stimulation elicits a beat-to-beat alternation in the action potential duratio
21 aim of this work was to investigate whether beat-to-beat alternation in the amplitude of the systoli
23 Alternans, a condition in which there is a beat-to-beat alternation in the electromechanical respon
24 henomenon of T-wave alternans (TWA) (i.e., a beat-to-beat alternation in the morphology and amplitude
25 complementary mechanism, CTA is caused by a beat-to-beat alternation in the number of refractory RyR
27 n the surface ECG was explained primarily by beat-to-beat alternation in the time course of cellular
28 CLs of 300 to 250 ms caused more pronounced beat-to-beat alternation of action potential duration (A
30 uced mild to moderate TWA principally due to beat-to-beat alternation of repolarization of cells in t
31 +) alternans is a potentially arrhythmogenic beat-to-beat alternation of the amplitude of the action
32 ns (TWA), an ECG phenomenon characterized by beat-to-beat alternation of the morphology, amplitude, a
33 a period doubling bifurcation, manifest as a beat-to-beat alternation, or alternans, of cardiac actio
35 ICaCC played a decisive role in shaping the beat-to-beat alternations in AP morphology observed duri
36 ular level, cardiac alternans is observed as beat-to-beat alternations in contraction strength, actio
37 ular level, cardiac alternans is observed as beat-to-beat alternations in contraction strength, actio
38 the cellular level alternans is observed as beat-to-beat alternations in contraction, action potenti
39 Cardiac alternans, described as periodic beat-to-beat alternations in contraction, action potenti
41 At the cellular level alternans manifests as beat-to-beat alternations in contraction, action potenti
42 ever, it remains an unresolved issue whether beat-to-beat alternations in intracellular Ca(2+) ([Ca(2
45 propagation became completely variable from beat to beat and thus transformed into fibrillatory cond
46 Cardiac myocyte intracellular calcium varies beat-to-beat and calmodulin (CaM) transduces Ca2+ signal
48 of Ca(2+) -activated Cl(-) channels reduced beat-to-beat AP alternations, but prolonged APD and fail
50 as characterized by significant increases in beat-to-beat atrial CL, MAPD, and diastolic interval var
52 ction to increases in myocardial demand on a beat-to-beat basis and mitochondrial calcium release dep
53 eleration of conduction was compensated on a beat-to-beat basis by an equal degree of slowing in the
55 gesting that NCX is regulated by Ca(2+) on a beat-to-beat basis during excitation-contraction couplin
58 low probe placed around the aortic root on a beat-to-beat basis in seven anesthetized open-chested ca
61 regulates CL in cardiac pacemaker cells on a beat-to-beat basis, and suggest a more realistic numeric
62 ther mitochondria take up Ca2+ rapidly, on a beat-to-beat basis, or slowly, by temporally integrating
70 al Doppler ultrasound along with noninvasive beat-to-beat blood pressure (BP), heart rate, and transc
72 microneurography, 12 paired recordings), and beat-to-beat blood pressure (BP; photoplethysmography) d
74 ontinuous heart rate (electrocardiogram) and beat-to-beat blood pressure (finger plethysmography) wer
75 temporal sequence over 5 years by recording beat-to-beat blood pressure and R-R intervals over 10 mi
76 ension, and orthostatic hypotension based on beat-to-beat blood pressure methods in a population-repr
78 urements of heart rate (ECG) and noninvasive beat-to-beat blood pressure recording (Finapres), with 5
80 bility may be the most reliable and specific beat-to-beat blood pressure variability metric due to it
84 od leading to vasovagal syncope we monitored beat-to-beat blood pressure, heart rate (HR) and forearm
85 s were instrumented for electrocardiography, beat-to-beat blood pressure, respiratory rate, CO-Modelf
86 tic nerve activity (MSNA; microneurography), beat-to-beat BP (photoplethysmography) and heart rate (e
89 nd frequency domain HRV indices, BRS, office beat-to-beat BP, and heart rate (HR) were measured for 1
92 paucity of existing literature investigating beat-to-beat BPV in clinically stable post-stroke patien
94 ive stress, also have deleterious effects on beat-to-beat [Ca(2+)](c) handling and excitation-contrac
96 Compared with BsCaM-2, BsCaM-45 tracks the beat-to-beat Ca2+-CaM alterations more closely following
98 c resonance imaging of brain and noninvasive beat-to-beat cardiovascular monitoring, we show that sti
101 ially mediating the association with greater beat-to-beat cerebral pulsatility (average DeltaMCA-PI v
102 early afterdepolarizations (EADs) result in beat to beat changes in the origin and direction of the
103 phic ventricular arrhythmias may result from beat to beat changes in wave propagation patterns initia
104 ith AF, no current models can both replicate beat-to-beat changes during AF and be fitted to individu
106 lts in acceleration and amplification of the beat-to-beat changes in cytosolic Ca(2+) in cardiomyocyt
108 Spectral transfer function gain between beat-to-beat changes in left ventricular end-diastolic p
109 2 (n = 2 out of 5) showed persistent complex beat-to-beat changes in nodal line formation of DA assoc
116 and exchangers, but are actively involved in beat to beat control of cardiac function by neural and h
118 t fluctuations in heart rate responsible for beat-to-beat control of heart activity, both at rest and
120 e oscillations are irregular and change from beat to beat due to the sensitivity of voltage repolariz
122 or blood pressure, quantification of complex beat-to-beat dynamics using multiscale entropy was able
123 frequency, kurtosis, and higher degree of a beat-to-beat electrogram similarity than areas without o
124 I sequences (RT-PC) can provide a continuous beat-to-beat flow signal that makes it possible to quant
127 veloped a computational model that simulates beat-to-beat haemodynamic changes resulting from the unc
128 e lacking the capabilities to both replicate beat-to-beat haemodynamic variations during AF at the sa
135 tion of the instantaneous variability of the beat-to-beat heart rate): spontaneous swallowing 12.02 +
140 al contractility is constantly changing from beat to beat in atrial fibrillation because of the influ
141 At 13 minutes, hemodynamics was analyzed beat-to-beat in the end-inspiratory and end-expiratory c
142 In these cardiomyocytes, which produce NO beat-to-beat, inhibition of mtNOS increased myocyte shor
145 multiscale complexity dynamics) measures of beat-to-beat interval variability were analyzed in two m
146 including standard deviation of the average beat to beat intervals over a 5-minute period, percentag
147 he NOX4 embryos displayed much more variable beat-to-beat intervals (mean S.D. of beat-to-beat interv
148 , the distributions of the variations in the beat-to-beat intervals for all healthy subjects are desc
150 nces and sample entropy, calculated from the beat-to-beat intervals of the PPG signal, to distinguish
151 ariable beat-to-beat intervals (mean S.D. of beat-to-beat intervals was 0.027 s/beat in control embry
152 fraction </= 45%) and sleep apnea underwent beat-to-beat measurement of SV by digital photoplethysmo
153 based techniques are less invasive and offer beat-to-beat measurements and excellent trending ability
154 ed neck chamber that was developed to enable beat-to-beat measurements of stroke volume using pulse-d
156 namics of the Starling mechanism, namely the beat-to-beat modulation of stroke volume (SV) caused by
157 a short, regular cycle length with identical beat-to-beat morphology, and the rest of the atria were
160 val and nonlinear analyses (newly developed, beat-to-beat nonlinear measurement of the repetitiveness
163 arization instability, manifested by TWA and beat-to-beat oscillations of T-wave amplitudes at other
170 udy was to determine the predictive value of beat-to-beat QT variability in heart failure patients ac
172 n the heart and the brain is pivotal for the beat-to-beat regulation of cardiac function and the clos
178 ctuations is reduced, and the time series of beat-to-beat RR intervals (RRIs) become highly non-stati
179 the fibrillatory cycle lengths with varying beat-to-beat sequences suggestive of unstable trajectori
181 rnative mechanisms, we measured simultaneous beat-to-beat stroke volume (flow) using Doppler echocard
186 2+) uniporter catalyzes Ca(2+) uptake during beat-to-beat transients of mitochondrial free Ca(2+), wh
188 phase to the DD later part, which exhibited beat-to-beat V(m) fluctuations with an amplitude of appr
191 mal culture conditions, MFS CMs show a lower beat-to-beat variability compared to corrected CMs using
193 surface lead electrocardiograms by analyzing beat-to-beat variability in ECG morphology using a smart
196 horter effective refractory periods, greater beat-to-beat variability of action potential durations,
197 horter effective refractory periods, greater beat-to-beat variability of action potential durations,
198 max boundaries was associated with increased beat-to-beat variability of conduction velocity and dire
200 d afterdepolarizations (DADs) and has a high beat-to-beat variability of repolarization (BVR) during
201 ease the action potential duration (APD) and beat-to-beat variability of repolarization (BVR) of APD
202 e of delayed afterdepolarizations (DADs) and beat-to-beat variability of repolarization (BVR) was hig
204 assessed by spectral analysis of spontaneous beat-to-beat variability of RR and QT intervals from sta
205 fidence interval, 1.7 to 9.3), and decreased beat-to-beat variability of the heart rate (odds ratio,
206 heir effect on the beating frequency and the beat-to-beat variability seemed largely independent of t
207 ery near the pulmonary vein ostia, and their beat-to-beat variability was greater than control (1.93+
209 28S abbreviated refractoriness and increased beat-to-beat variability, leading to early afterdepolari
210 ice insertion, transmitral flow showed rapid beat to beat variation in each patient, from abnormal re
211 nchronous LV assistance produced significant beat to beat variation in filling indexes, but overall a
220 whereas ERP restitution underlies temporal, beat-to-beat variations in refractoriness during rapid p
224 ibility study by 2 leadless pacemakers using beat-to-beat, wireless communication, achieving a succes
226 hat varied its location and orientation from beat to beat, with the majority of ventricular myocardiu