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1 echogenic intracardiac focus (ie, calcified papillary muscle).
2 on and lateral displacement of the posterior papillary muscle.
3 ocardial infarction, including the posterior papillary muscle.
4 t and no-flow ischemia in an isolated rabbit papillary muscle.
5 n of leaflet tissue attached to the anterior papillary muscle.
6 yocardium near the insertion of the anterior papillary muscle.
7 the wall of the left ventricle overlying the papillary muscle.
8 r LV free wall near the root of the anterior papillary muscle.
9 into the myocardium underlying the infarcted papillary muscle.
10 bundles isolated from mouse left ventricular papillary muscles.
11 annular dilatation with displacement of the papillary muscles.
12 he ventricle and improved orientation of the papillary muscles.
13 ional changes were also assessed in isolated papillary muscles.
14 fibre bundles prepared from left ventricular papillary muscles.
15 raction is described in 25 reperfused rabbit papillary muscles.
16 ule depolymerization in both control and PAB papillary muscles.
17 ed IGF-1-positive inotropic action in ferret papillary muscles.
18 aequorin-loaded rat whole hearts and ferret papillary muscles.
19 mRNA expression in stretched and unstretched papillary muscles.
20 nulus and its spatial relationship with both papillary muscles.
21 e stretch activation response of the cardiac papillary muscles.
22 on (MI), with leaflet tethering by displaced papillary muscles.
23 o displaced the posterior annulus toward the papillary muscles.
24 elaxation in both isolated hearts and intact papillary muscles.
25 strating enlarged interventricular septa and papillary muscles.
26 tion (61 %) or relaxation (59 %) of isolated papillary muscle, (2) fractional shortening (50 %), ampl
28 s (14% decrease in peak developed pressure), papillary muscles (53% decrease in maximum developed for
31 force recovered to 60 +/- 3 % (n = 7) in NTG papillary muscles, 98 +/- 2 % (n = 5) in muscles from TG
33 on the leaflets due to displacement of their papillary muscle and annular attachments, which restrict
34 lar cavity and the direct continuity between papillary muscle and anterior leaflet associated with a
35 lic mitral annulus dimensions, components of papillary muscle and leaflet displacement, were calculat
36 he tethering line connecting the annulus and papillary muscle and reflects limitation of anterior mot
37 of leaflet tissue attached to the posterior papillary muscle and restriction of leaflet tissue attac
38 ction potentials were recorded from isolated papillary muscle and sinoatrial node by microelectrode t
39 e that increases isometric force in isolated papillary muscle and the extent of shortening in isolate
41 osin in distinct areas such as at the tip of papillary muscles and at the base close to the valvular
43 s, with a wide array of malformations of the papillary muscles and chordae, that can be detected by t
47 x-ray microanalysis (EPMA) of rapidly frozen papillary muscles and trabeculae incubated with ryanodin
48 er in 6 of 6 cardiac arrest patients (4 from papillary muscle) and Purkinje origin of dominant VE was
49 function were assessed by echocardiographic, papillary muscle, and isolated cardiomyocyte studies.
50 quence similar to sinus rhythm or arose near papillary muscles, and (2) stable pattern, in which acti
51 oronary snare and marker placement (annulus, papillary muscles, and anterior and posterior leaflets).
52 impairment of lateral shortening between the papillary muscles, and not passive ventricular size, tha
53 rdium interface in areas of trabeculation or papillary muscles, and of the atrioventricular ring.
54 urements (perfused isolated hearts, isolated papillary muscles, and skinned fiber preparations), bioc
56 zing restrictive mitral annuloplasty (RA) or papillary muscle approximation with undersizing restrict
58 -dimensional relationship of the annular and papillary muscle attachments of the valve so as to incre
59 the anterior wall, one set at the tip of the papillary muscle (basal) and one at the site of papillar
60 , the force-frequency relationships of mouse papillary muscle bundles were measured in the presence o
61 ntegrin, depresses the force production from papillary muscle bundles, partly associated with changes
63 ted the hypothesis that repositioning of the papillary muscles can be achieved by injection of polyvi
64 roapical extension can mechanically displace papillary muscles, causing MR despite the absence of bas
65 erences were estimated at a tissue (isolated papillary muscle), cellular (isolated left ventricular c
67 ulted from maintenance of the mitral annular papillary muscle continuity during mitral valve repair.
69 display a predisposition for trabecular and papillary muscle defects, ventricular septal defects, co
70 valve replacement, the technical problems of papillary muscle dehiscence and mitral regurgitation app
71 -skinned fiber bundles from left ventricular papillary muscle demonstrated a significant inhibition o
73 mmetrical mitral annular (MA) dilatation and papillary muscle dislocation are implicated in the patho
74 e from infarction or cardiomyopathy produces papillary muscle displacement and annular dilatation, ca
76 over time with mechanical stretch created by papillary muscle displacement through cell activation, n
77 ateral annular dilatation, lateral posterior papillary muscle displacement, and apical PL restriction
78 stress, function, and sphericity) and local (papillary muscle displacements and regional wall motion
83 chanical stretch of the inferobasal wall and papillary muscles, eventually leading to myocardial hype
84 train relations in resting right ventricular papillary muscles exhibited 60% greater strains (P:<0.01
85 t rate and resonant frequency of the cardiac papillary muscles expressing the mutant essential light
88 ead morphology, can help distinguish between papillary muscle, fascicular, and mitral annular VAs.
89 Patients undergoing catheter ablation for papillary muscle, fascicular, or mitral annular VAs were
90 in detergent-treated mouse left ventricular papillary muscle fiber bundles where the endogenous trop
92 creased approximately 20% in Tg-E22K skinned papillary muscle fibers and intracellular [Ca2+] and for
93 f the ATPase and force in transgenic skinned papillary muscle fibers from mutated versus control mice
95 ients were significantly decreased in intact papillary muscle fibers from Tg-E22K compared to Tg-WT m
96 e were generated, and the skinned and intact papillary muscle fibers from the Tg-D166V mice were exam
99 gle myosins in relaxed permeabilized porcine papillary muscle fibers indicated slightly differently o
102 echanical coupling deficits, we compared the papillary muscle force generated by electrically stimula
103 on fraction, systolic blood pressure, and LV papillary muscle force while LV end-diastolic and systol
104 r dilatation, leaflet tethering by displaced papillary muscles frequently induces mitral regurgitatio
106 arction, total displacement of the posterior papillary muscle from the midseptal annulus ("saddle hor
107 ilarly, the contractile behavior of isolated papillary muscles from diabetic SERCA2a mice was not dif
108 ong the muscle fibers or in fiber tension in papillary muscles from heterozygous global Vcl null mice
109 gitation (MR) relates to displacement of the papillary muscles from ischemic ventricular distortion.
111 anical protocol to isometrically contracting papillary muscles from two rabbit heart populations: (1)
112 determine the mechanism by which annular and papillary muscle geometric alterations result in MR, we
115 mias (VAs) arising from the left ventricle's papillary muscles has been associated with inconsistent
118 transients in electrically stimulated intact papillary muscles; however, the R58Q mutation also resul
122 rane potential was recorded in 10 guinea pig papillary muscles in a tissue bath using a double-barrel
123 is was detected at histology at the level of papillary muscles in all patients, and inferobasal wall
124 arction (MI), leaflet tethering by displaced papillary muscles induces mitral regurgitation (MR), whi
126 In HCM, outflow obstruction due to anomalous papillary muscle insertion directly into anterior mitral
127 er in 1997 who demonstrated direct anomalous papillary muscle insertion into the anterior mitral leaf
128 on induces an unloading of myocardium at the papillary muscle insertion site and that the resulting h
130 m(2)), and lack of echocardiographic scar at papillary muscle insertion sites (all P<0.05) and, when
131 eline had a 106 +/- 74 ms time delay between papillary muscle insertion sites (p < 0.001 vs. normal).
132 ordinated timing of mechanical activation of papillary muscle insertion sites appears to be a mechani
133 ults from improved coordinated timing of the papillary muscle insertion sites, using the novel approa
134 argins of the mitral leaflet unencumbered by papillary muscle insertion, and in 1 patient probably re
137 lso determined the kinetics of relaxation of papillary muscles isolated from all four groups of anima
138 to the obstacle and another attaches to the papillary muscle, it may result in stable VT with figure
139 deling (apical and posterior displacement of papillary muscles) leads to excess valvular tenting inde
140 was created within the ventricular septum to papillary muscle level; also, in 1 patient, attachment o
141 ilization by an external patch device of the papillary muscle-LV wall complex that controls mitral va
142 al echocardiographic examination for erratic papillary muscle motion in all patients with suspected r
143 ersus 3.1+/-2.7 (P=0.02), with the posterior papillary muscle moving more laterally (6.8+/-3.4 versus
144 (32 [63%] male; mean age 61+/-15 years) with papillary muscle (n=18), fascicular (n=15), and mitral a
145 n=37; 38.1%), LV trabeculations (n=5; 5.2%), papillary muscle (n=3; 3.1%), and apical-septal bundle (
148 ation normalized myocardial contractility in papillary muscles of PAB cats but did not alter contract
149 ications of catheter ablation of VA from the papillary muscles of the left ventricle with either cryo
152 from the outflow tract alternating with the papillary muscle or fascicular region (7 of 9 [78%] vs.
153 oci being mapped at either the anterolateral papillary muscle or posteromedial papillary muscles of t
155 aim of this study was to define the role of papillary muscles (PAPs) in post-infarction ventricular
156 we sought to identify mitral valve (MV) and papillary muscle (PM) abnormalities that predisposed to
158 ) has been attributed to annular dilatation, papillary muscle (PM) displacement ("apical leaflet tent
163 cle, 8 on the mitral annulus (MA), 1 on each papillary muscle (PM) tip, and 1 on the anterior and pos
166 try and dynamics of the mitral annulus (MA), papillary muscle (PM), and the chordae tendineac, chorda
170 me was increased tethering distance from the papillary muscles (PMs) to the anterior annulus, especia
171 et tethering by displaced attachments to the papillary muscles (PMs), it is incompletely treated by a
173 implanted to silhouette the LV, annulus, and papillary muscles (PMs); 3 transmural bead columns were
175 veloped that allows independent variation of papillary muscle position, annular size, and transmitral
176 r dilatation increased regurgitation for any papillary muscle position, creating clinically important
178 igated in an isolated, blood-perfused rabbit papillary muscle preparation with a confined extracellul
182 ocardiograms of 21 consecutive patients with papillary muscle rupture (20 involved the left ventricle
184 The single patient with right ventricular papillary muscle rupture showed erratic motion as well a
185 ses include right ventricular infarction and papillary muscle rupture with acute severe mitral regurg
186 left ventricle is useful in the diagnosis of papillary muscle rupture, especially in those patients i
188 7 (35%) of 20 patients with left ventricular papillary muscle rupture, the ruptured head was not seen
190 e as the left ventricle (LV) dilated and the papillary muscles shifted posteriorly and mediolaterally
191 s force and [Ca(2+)]i measurements on intact papillary muscles show that enhancement of relaxation in
192 orce and [Ca(2+)]in measurements in isolated papillary muscles showed that the increased force and tw
193 s prominent erratic motion or flutter of the papillary muscle still attached to the left ventricular
195 nical properties of skinned left ventricular papillary muscle strips from mouse hearts bearing the R4
197 s study sought to investigate the benefit of papillary muscle surgery on long-term clinical outcomes
201 extending to the inferior apex displaces the papillary muscles, tethering the mitral leaflets to caus
202 ium while at the same time repositioning the papillary muscles that become apically tethered in MR.
204 ithin the body and to study the integrity of papillary muscles, the fibrous tissue of cardiac valve a
206 ps: 1) markedly increased r of the posterior papillary muscle tip (10.3 versus 6.4 mm, MR versus no-M
207 its attachments to the anterior annulus and papillary muscle tip (angular difference = 3 +/- 7 degre
208 the intercommissural dimension with anterior papillary muscle tip displacement toward the annulus is
209 a (MAA), anterior (APM), and posterior (PPM) papillary muscle tip distances to midseptal MA ("saddle
211 end-systole) and increased r of the anterior papillary muscle tip; 2) dilation (in the septal-lateral
212 anterior and posterior mitral leaflets, and papillary muscle tips and bases in 2 groups of sheep.
214 ETHODS AND Under cardiopulmonary bypass, the papillary muscle tips in 6 adult sheep were retracted ap
216 creasing the leaflet tethering distance from papillary muscle tips to the anterior mitral annulus (P<
217 markers were sutured to the mitral annulus, papillary muscle tips, and leaflet edges in 13 sheep.
218 ords at anterior mitral leaflet (S1 and S2), papillary muscle tips, fibrous trigones, mitral annulus,
219 illow height (P<0.0001), longer lengths from papillary muscles to coaptation (P<0.0001), and more fre
220 cTnC for the thin filament in reconstituted papillary muscles to provide evidence of an allosteric m
221 e with MR (>/= moderate) had higher systolic papillary muscle-to-annulus tethering length (P < 0.01).
222 was associated with a decrease in infarcted papillary muscle-to-mitral annulus tethering distance (2
225 thm, the accuracy rates for the diagnosis of papillary muscle VAs, fascicular VAs, and mitral annular
226 syndrome is characterized by fascicular and papillary muscle VE that triggers ventricular fibrillati
227 tion, the normal shortening of the posterior papillary muscle was obliterated to allow its tip to mov
228 n of isolated rat left ventricular posterior papillary muscle was virtually eliminated at the end of
230 and cryostat sections of rat left ventricle papillary muscles, we localized AKAP100 to the nucleus,
231 oporation and conduction block thresholds in papillary muscles were 281+/-64 V and 380+/-79 V, respec
235 transients in electrically stimulated intact papillary muscles were observed in Tg-R145G compared wit
238 o, in 1 patient, attachment of anterolateral papillary muscle with the lateral free wall was partiall
239 staining of transverse cross-sections of the papillary muscles with AKAP100 plus alpha-actinin-specif
240 0.75) and posterior (r=0.70) displacement of papillary muscle, with confirmation in multivariate anal
241 rated anterior displacement of hypertrophied papillary muscles within the left ventricular cavity and
242 or motion relative to the posteriorly placed papillary muscles without a decrease in total orifice ar
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