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1 ogressive symptomatic heart failure and left ventricular dilation.
2 ic regurgitation complicated by extreme left ventricular dilation.
3 ile function, decreased work capability, and ventricular dilation.
4 h, associated with eccentric hypertrophy and ventricular dilation.
5 However, MMPi reduced ventricular dilation.
6 city and contractile function and attenuated ventricular dilation.
7 racterized by impaired systolic function and ventricular dilation.
8 Only L-NAME caused right ventricular dilation.
13 ized mice to cardiac decompensation and left ventricular dilation after long-term stimulation by pres
15 ed the clinical manifestation of human ARVC: ventricular dilation and aneurysm, cardiac fibrosis, car
16 ed CD34+ cells (CD34(Shh)) protected against ventricular dilation and cardiac functional declines ass
18 ar (LV) fractional shortening accompanied by ventricular dilation and decreased phosphocreatine to AT
19 c analysis demonstrated the presence of left ventricular dilation and decreased systolic function in
20 ion with 3 months follow-up resulted in left ventricular dilation and dysfunction in both wild-type a
21 systole, left ventricular dysfunction, right ventricular dilation and dysfunction, and a large perica
22 ardial iNOS expression, cardiac hypertrophy, ventricular dilation and dysfunction, and fibrosis, wher
26 ion of recombinant GDF15 protein, attenuated ventricular dilation and heart failure in muscle lim pro
30 re 85+/-1 versus 66+/-2 mm Hg; P<0.01), left ventricular dilation and hypertrophy (mass/body weight 4
31 iotensin-converting enzyme inhibition limits ventricular dilation and hypertrophy and improves surviv
33 mmunocomplexes followed by cardiomegaly with ventricular dilation and hypertrophy, ultimately succumb
34 athic dilated cardiomyopathy had evidence of ventricular dilation and hypokinesis, with a left ventri
35 Mutant G202R and A592E mice exhibited left ventricular dilation and impaired function with specific
37 more than wild type, along with greater left ventricular dilation and increased fibrosis, apoptosis,
39 nges were associated with reductions in left ventricular dilation and left ventricular mass measured
41 during atrial arrhythmia are those with left ventricular dilation and low atrial ejection fraction ac
43 3+, fibrillation (vs. type I flutter), left ventricular dilation and mitral valve area < 2.0 cm2.
44 hat IL-1beta and TNF-alpha may contribute to ventricular dilation and myocardial failure by promoting
46 hallium lung-to-myocardial ratio (L/M), left ventricular dilation and perfusion defect site were comp
48 The engrafted human myocardium attenuated ventricular dilation and preserved regional and global c
49 car with newly formed myocardium, attenuated ventricular dilation and prevented the chronic decline i
52 graphy of homozygous mutant mice showed left ventricular dilation and reduced contractile function at
53 Systolic heart failure is characterized by ventricular dilation and reduced ejection fraction, and
54 ted myocytes was depressed and preceded left ventricular dilation and reduced fractional shortening.
55 +cell hearts exhibited attenuation of global ventricular dilation and reduced septum-to-free wall dia
56 lso enhance late survival by preventing left ventricular dilation and reducing arrhythmias, independe
57 ath and low rate of reintervention for right ventricular dilation and residual outflow tract obstruct
59 s of afterload reduction for preventing left ventricular dilation and symptom onset in aortic regurgi
60 ilated cardiomyopathy, characterized by left ventricular dilation and systolic dysfunction with signs
63 endent increase in cardiac hypertrophy, left ventricular dilation, and adverse left ventricular remod
64 entricular ejection fraction <40%, mild left ventricular dilation, and no symptoms of heart failure (
65 developed greater cardiac hypertrophy, left ventricular dilation, and reduced contractile function.
66 eccentric hypertrophy, substantial fibrosis, ventricular dilation, and reduced fractional shortening,
67 r rates of cardiac rupture, more severe left ventricular dilation, and suppressed ejection fraction c
68 ascular-specific expression (vGOF) show left ventricular dilation as well as less-markedly increased
69 db/db animals, dbTSP mice had increased left ventricular dilation associated with mild nonprogressive
71 , congestive heart failure, and greater left ventricular dilation at diagnosis were independently ass
72 uld not be attributed to differences in left ventricular dilation because end-diastolic volumes incre
73 sion maintenance and increased resistance to ventricular dilation) but also for a potentially deleter
75 ice, loss of cMyBP-C has been linked to left ventricular dilation, cardiac hypertrophy, and systolic
76 age, heterozygous individuals developed left ventricular dilation, contractile dysfunction, and episo
77 decline in cardiac function, attenuated left ventricular dilation, decreased infarct size, and reduce
78 exacerbated, as indicated by increased left ventricular dilation, decreased ventricular function, in
80 ed in aortic regurgitation with extreme left ventricular dilation (diastolic dimension >/= 80 mm), bu
85 ks of pressure-overload stimulation, reduced ventricular dilation, enhanced ventricular performance,
86 erload developed less hypertrophy and showed ventricular dilation, impaired contractile function, inc
88 eart failure therapy indexed by reduced left ventricular dilation, improved left ventricular ejection
89 p to day 56 after MI revealed increased left ventricular dilation in CD4 KO compared with WT mice.
90 iction (TAC) for 6 weeks caused greater left ventricular dilation in G6PDX mice than wild-type mice.
91 iography showed significantly increased left ventricular dilation in male IL-13(-/-) compared with WT
93 Advanced age is a predictor of death and ventricular dilation in patients with MI; however, the c
94 -/-) animals lack a corpus callosum and show ventricular dilation indicating early hydrocephalus.
96 severe cardiac abnormalities, including left ventricular dilation, left ventricular mass reduction, a
98 viable myocardium after infarction, limiting ventricular dilation, myocardial loading, and cardiac hy
102 muscle disorder characterized by atrial and ventricular dilation often with relative wall thinning,
105 ntriculomegaly due to either posthemorrhagic ventricular dilation or periventricular white matter los
106 of increased wall thickness, local or global ventricular dilation, or dysfunction also involved the R
107 cular ejection fraction (p = 0.006) and left ventricular dilation (p = 0.015) at the follow-up evalua
108 tolic dimension >/= 80 mm), but extreme left ventricular dilation raises concern about irreversible l
109 protein composition, loss of cardiomyocytes, ventricular dilation, reduced pump function, and ultimat
110 particularly severe myocardial fibrosis with ventricular dilation, reminiscent of the dilated cardiom
112 ated cardiomyopathy is characterised by left ventricular dilation that is associated with systolic dy
113 d cellular hypertrophy, are concomitant with ventricular dilation, thinning of the wall and cardiac d
114 nd indicates severe symptoms (hydrocephalus, ventricular dilation), treatment is continued until deli
115 rapidly progressive cardiomyopathy with left ventricular dilation, wall thinning, and reduced systoli
123 sis of embryos revealed evidence of profound ventricular dilation, which likely resulted in embryonic
124 l infarction (MI) developed progressive left ventricular dilation with dysfunction and HF at 4 wk pos
126 infarction and exhibit significantly limited ventricular dilation with sustained and remarkably enhan
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