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1 existing cardiovascular disease or calcific aortic valve stenosis.
2 tain high-risk surgical patients with severe aortic valve stenosis.
3 ctor for cardiovascular disease and calcific aortic valve stenosis.
4 mic and functional characteristics of severe aortic valve stenosis.
5 functional properties of severe degenerative aortic valve stenosis.
6 or cardiovascular disease (CVD) and calcific aortic valve stenosis.
7 for treatment of severe symptomatic calcific aortic valve stenosis.
8 e best approach to treat neonatal congenital aortic valve stenosis.
9 PPM and regression of SMR following AVR for aortic valve stenosis.
10 alve thickening to severe calcification with aortic valve stenosis.
11 enic signaling, and halts the progression of aortic valve stenosis.
12 entify therapeutic targets for prevention of aortic valve stenosis.
13 rdiographic findings in patients with severe aortic valve stenosis after transcatheter aortic valve r
18 ies that highlight Lp(a) in CVD and calcific aortic valve stenosis and propose pathways to clinical r
19 d Lp(a) is causally associated with calcific aortic valve stenosis and the need for aortic valve repl
21 tive cardiomyopathy (HOCM), 10 patients with aortic valve stenosis, and 14 healthy individuals using
22 nvasive diagnostic tool in the assessment of aortic valve stenosis, and how the results compare with
23 are clinical risk factors for development of aortic valve stenosis, and hypercholesterolemia is a put
24 nto the haemodynamic cardiac consequences of aortic valve stenosis (AS) and aortic valve regurgitatio
35 A region was associated with the presence of aortic valve stenosis (AVS), no prospective study has su
38 s assessed by FFR in 54 patients with severe aortic valve stenosis before and after transcatheter aor
39 ctor for cardiovascular disease and calcific aortic valve stenosis, but no approved specific therapy
42 f hypertrophy was also seen in patients with aortic valve stenosis: ERK(Thr188) phosphorylation was i
44 nts, and risk factors described for critical aortic valve stenosis have been shown to be inapplicable
45 en have a better prognosis when experiencing aortic valve stenosis, hypertrophic cardiomyopathy, or h
46 ortic valve sclerosis was present in 26% and aortic valve stenosis in 2% of the entire study cohort;
47 risk of cardiovascular disease and calcific aortic valve stenosis in patients with elevated Lp(a) co
52 or redo TAVR were moderate-severe prosthetic aortic valve stenosis (n=10, 21.7%), moderate-severe cen
54 aortic valve is frequently an antecedent to aortic valve stenosis or insufficiency and is often asso
55 ion of pathophysiological conditions such as aortic valve stenosis or insufficiency, making it possib
56 w-up measurements were performed in HOCM and aortic valve stenosis patients 4 months after surgery.
57 in FFR values was found before and after the aortic valve stenosis removal (0.89+/-0.10 versus 0.89+/
59 ons for diseases such as atherosclerosis and aortic valve stenosis, since it strongly suggests a gene
60 t to randomize all-comers with severe native aortic valve stenosis to either transcatheter aortic val
62 from the right sinus of Valsalva, congenital aortic valve stenosis (with bicuspid valve) and myocardi
64 tested the hypothesis that calcification and aortic valve stenosis would develop in genetically hyper
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