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1 sed for studies of neointima hyperplasia and arterial stenosis.
2 for TAG functional assessment of a coronary arterial stenosis.
3 no benefit in suppressing the development of arterial stenosis.
4 CCR2 as a viable therapeutic target for NF1 arterial stenosis.
5 ial atherosclerosis increases with degree of arterial stenosis.
6 terial definition, venous contamination, and arterial stenosis.
7 nd progression of neointimal hyperplasia and arterial stenosis.
8 e to warfarin for patients with intracranial arterial stenosis.
9 n assessing the clinical importance of renal arterial stenosis.
10 ve a predisposition for premature and severe arterial stenosis.
11 assessed for location and extent of carotid arterial stenosis.
12 + cells did not correlate with the degree of arterial stenosis.
13 t contributes to the development of critical arterial stenosis.
14 nformation in vivo, we used a mouse model of arterial stenosis.
15 k patients with atherosclerotic intracranial arterial stenosis.
16 timal proliferation in a murine model of NF1 arterial stenosis.
20 diarrhea, sphincter of Oddi dysfunction and arterial stenosis; all responded to directed treatments.
21 mmunities relates to the correlation between arterial stenosis and acute ischaemic events, including
22 hologies associated with thrombosis, such as arterial stenosis and myeloproliferative neoplasms (MPNs
23 mild, transient graft damage due to gradual arterial stenosis and the development of arterial collat
24 for months to years; LMP causes progressive arterial stenosis and thrombosis and is composed of uniq
25 iovascular abnormalities, including pulmonic arterial stenosis and ventricular septal defects accompa
26 on individual "vulnerable plaque," coronary arterial stenosis, and inducible myocardial ischemia to
27 FMD is a systemic arteriopathy presenting as arterial stenosis, aneurysm, and dissection in virtually
29 l MR DSA improves the delineation of carotid arterial stenosis by virtually eliminating saturation ef
31 ozygous Nf1 (Nf1(+/-)) mice develop a marked arterial stenosis characterized by proliferating smooth
32 f renal transplant arteries and detection of arterial stenosis comparable with those at contrast-enha
33 grade and hemodynamic significance of renal arterial stenosis, diagnostic quality, and presence of a
34 VEC MR imaging at baseline, single coronary arterial stenosis, dipyridamole stress, and reactive hyp
35 PAD) is characterized by varying severity of arterial stenosis, exercise induced claudication, malper
36 tential novel therapeutic approach to reduce arterial stenosis following revascularization in CAD and
37 which is based on the concept that occlusive arterial stenosis generally provokes ischaemic events.
40 specificity (92%) for the detection of renal arterial stenosis, including all four distal stenoses en
45 hed definitions; FCA was defined as cerebral arterial stenosis not attributed to specific diagnoses s
48 multiphoton microscopy revealed that in vivo arterial stenosis of a damaged carotid artery markedly i
50 a non-lacunar brain infarct without proximal arterial stenosis or cardioembolic sources, with a clear
51 flow reserve and (a) assessments of coronary arterial stenosis severity by quantitative coronary angi
52 renal arterial stenosis, kidneys with renal arterial stenosis showed 50% (0.14/0.28) EF reduction (P
54 ry groups, an approximately 50% reduction in arterial stenosis was observed with targeted NP treatmen
56 0.44 to 3.57+/-0.65 and 3.45+/-0.58 mm2, and arterial stenosis was reduced from 58+/-11% to 37+/-8% a
58 icity of DSC CT for detecting 50% or greater arterial stenosis were calculated by using a bivariate s
60 ading to graft loss, whereas two episodes of arterial stenosis were successfully treated with percuta
61 sal status is a risk factor for intracranial arterial stenosis when compared with premenopausal statu
62 R 1.42, 95% CI 0.96 to 2.10) and ipsilateral arterial stenosis with 50%-99% narrowing (HR 1.54, 95% C