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1 eling of follicular epithelium (also called 'patency').
2 RA was found to be patent in 24 cases (84.8% patency).
3 oups (67.4% versus 65.7%, P=0.92 for primary patency).
4 recurrent restenosis (100% rate of Secondary patency).
5 rements and implications for long-term graft patency.
6 conduit function and possibly improve graft patency.
7 he primary end point was 3-year angiographic patency.
8 significantly influenced long-term RA graft patency.
9 rinolysis to physiologically maintain vessel patency.
10 motoneurons important for maintaining airway patency.
11 nd/MRI were used subsequently to document PV patency.
12 e muscles of respiration and maintain airway patency.
13 c evidence of ostium patency and canalicular patency.
14 lesion revascularization and loss of primary patency.
15 activation of canonical Wnt causes PF-suture patency.
16 offers a promising target for modulating DA patency.
17 nical challenge in determining tibial artery patency.
18 r to LITA patency and is much better than SV patency.
19 ebs, may also have adverse effects on airway patency.
20 ent prognostic factors associated with stent patency.
21 xhibited a delay in the onset of blood-stage patency.
22 nt benefit of statin treatment on vein graft patency.
23 amages peri-infarct tissue, despite arterial patency.
24 y invasive method for reestablishing luminal patency.
25 s vein graft disease, and improve vein graft patency.
26 vein graft did not result in greater 1-year patency.
27 ntity; increased Eph-B activity improves AVF patency.
28 clot stability and maintaining blood vessel patency.
29 recoil, when it did occur, did not influence patency.
30 e showing obstruction and the second showing patency.
31 ic recoil and determine its effect on access patency.
32 associations are explained by reduced airway patency.
33 isted patency, and 89% (74-93) had secondary patency.
34 a improved medium-term arteriovenous fistula patency.
35 d a preservation of the entire vascular tree patency.
36 al and uterine morphology and fallopian tube patency.
40 , 63% (95% CI 47-72) of patients had primary patency, 73% (57-81) had primary assisted patency, and 9
42 (22.4% vs. 41.9%, p = 0.019), greater vessel patency (75.0% vs. 57.1%, p =0.025), and similar death,
43 TA per the Kaplan-Meier estimate for primary patency (89.0% versus 65.0% at 365 days; log-rank P<0.00
44 on to Inhibit Restenosis and Maintain Vessel Patency-A Pilot Study of Anti-Restenosis Treatment) was
49 f GpIbalpha-VWF interactions restores vessel patency after occlusive thrombosis by specifically disag
50 aphic (US) nephrostograms to assess ureteral patency after percutaneous nephrolithotomy (PCNL) in thi
53 us methods that can be used to measure nasal patency, airflow and resistance, mainly peak nasal inspi
55 in the poststenotic kidney, restoring vessel patency alone is insufficient to recover kidney function
56 ine associated with primary unassisted graft patency among participants in a randomized trial that co
57 llow-up, the incidence of primary unassisted patency among participants using aspirin at baseline was
58 use was also associated with improved lesion patency among patients undergoing infrapopliteal angiopl
60 mation exists on the intermediate-term graft patency and 5-year clinical outcomes of patients receivi
63 may be useful for predicting long-term graft patency and assessing grafts intraoperatively in patient
65 conducted to assess whether DES also improve patency and clinical outcome of infrapopliteal lesions.
66 propriate conduit to improve long-term graft patency and clinical outcomes of patients undergoing CAB
67 thrombi resulting in fast restoration of MCA patency and consequently reduced cerebral infarct sizes
69 ing GpIbalpha-VWF inhibitors restored vessel patency and improved outcome in a mouse model of ischemi
70 c arteries (BITA) have demonstrated superior patency and improved survival in patients undergoing cor
71 data may be helpful in predicting long-term patency and in the decision of whether to revise a quest
76 vened segments, both of which may jeopardize patency and lead to recurrent symptoms, functional impai
79 iker-Fuse nucleus (KF) controls upper airway patency and regulates respiration, in particular the ins
81 n angioplasty strategy has equivalent 1-year patency and should be preferred over primary stenting.
85 TTP was inversely correlated with vascular patency and verteporfin uptake, suggesting interstitial
86 ts were evaluated with objective (anatomical patency) and subjective (symptomatic cure) success rates
88 ry patency, 73% (57-81) had primary assisted patency, and 97% (85-98) had secondary patency, with mos
89 , with late luminal enlargement, side-branch patency, and development of a signal-rich, low-attenuati
91 Cs displayed good attachment, stabilization, patency, and typical vascular structure when seeded on d
92 of aggressive statin treatment on vein graft patency are required, in order to safely translate this
94 and as good an indication of objective nasal patency as formal rhinomanometry and has the advantage t
95 or maturation of schistosomes in the host to patency, as we reproducibly recovered significantly fewe
96 mary efficacy assessment was change in nasal patency assessed by measuring the minimal cross-sectiona
98 ndary end points included angiographic graft patency at 1 week after CABG, myocardial infarction, str
99 was no significant difference in study graft patency at 1 year after CABG (radial artery, 238/266; 89
101 reated with the helical stent who maintained patency at 12 and 24 months was 80% and 72%, respectivel
103 coated balloon resulted in a rate of primary patency at 12 months that was higher than the rate with
105 dimensions and function, and aortic size and patency at 14.1 +/- 1.2 months and 33.6 +/- 9.6 months i
108 te (primary, primary assisted, and secondary patency at 6 and 12 months), (2) improvement of quality
109 nhibitor treatment effectively improved TEVG patency at 6 mo compared to the untreated control group
113 esions demonstrated significant clinical and patency benefits for heparin-bonded covered stents compa
117 x; (b) >50% patent but some reflux; (c) some patency but >50% reflux; or (d) nonpatent, 100% reflux.
122 study was to determine whether upper airway patency can be improved using chemogenetic approach by d
123 DES group exhibited superior 2-year primary patency compared with the provisional BMS group (83.4% v
126 The primary efficacy end point was primary patency, defined as freedom from restenosis or clinicall
127 e primary study end point was 1-year primary patency, defined as freedom from target-lesion restenosi
128 and cell seeding to investigate the vascular patency, degree of decellularization, and scaffold bioco
129 plete recovery, aesthetic, functional (nasal patency, eye closure, speech and swallowing) and psychol
132 reconstructed rat aorta confirmed equivalent patency, flow and burst strength, and histological analy
133 false lumen thrombosis (FLT) and false lumen patency (FLP) was determined and the effect on post-TEVA
134 resulted in significantly lower FitzGibbon A patency for arterial and saphenous vein graft conduits a
135 deled probabilities of primary and secondary patency for each access type, with success modified by a
136 tents and drug-coated balloons have improved patency for moderate-length lesions, whereas others allo
137 The 24-month assessments included primary patency, freedom from clinically driven target lesion re
139 ested EVH is associated with decreased graft patency, higher rates of cardiovascular complications (e
141 and CC angiographic imaging regarding graft patency in 114 of 115 grafts identified with CC angiogra
142 olysis In Myocardial Infarction flow grade 3 patency in 15% of patients with acute myocardial infarct
143 ate platelet-rich thrombi and restore vessel patency in acute thrombotic disorders such as ischemic s
147 the importance of including vascular access patency in future studies of BP management in hemodialys
148 CS CABG Patency Study showed excellent graft patency in patients assessed by 64-slice computed tomogr
149 bypass grafting because they have excellent patency in patients with and without diabetes even after
150 use in the assessment of allograft vascular patency in patients with graft dysfunction, either delay
151 creasingly used to maintain long-term venous patency in patients with iliofemoral venous outflow obst
154 eHAT is initially asymptomatic and arterial patency is monitored with percutaneous Doppler ultrasoun
155 n for the purpose of maintaining canalicular patency is not necessary when performing endonasal DCR i
157 artery stenosis, we hypothesized that graft patency is worse in patients with than without diabetes.
158 tion of liver burden and delayed blood-stage patency, leading to a disease outcome different from tha
159 sponse that influences vessel remodeling and patency, limiting long-term benefits of cardiovascular i
160 The Kaplan-Meier analysis for time to first patency loss was not significantly different (log rank =
161 versus PTA with significantly higher primary patency, lower CD-TLR, and similar functional status imp
163 ocardial infarction; superior infarct artery patency, no reocclusions, and 1% mortality resulted.
164 target-lesion revascularization and loss in patency, no significant differences prevailed between th
166 ]; Asp/Pla) therapy achieved nearly half the patency observed in the SCID/bg mouse (NK Ab: 0.356 +/-
174 uct cancer patients and results in prolonged patency of hilar bile ducts, a trend for longer survival
175 s, diabetes was associated with higher early patency of ITA grafts (odds ratio: 0.63; 95% confidence
176 e limits: 0.43 to 0.91; p = 0.013), but late patency of ITA grafts was similar in patients with and w
177 (ERDP/ASA) prolongs primary unassisted graft patency of newly created hemodialysis arteriovenous graf
178 ith a trend toward longer primary unassisted patency of newly placed hemodialysis grafts similar to t
182 oading based on the contractility state, the patency of the actin cytoskeleton, and the connections i
184 E(2)) plays a major role both in maintaining patency of the fetal ductus arteriosus and in closure of
187 The primary efficacy end point was primary patency of the target lesion at 12 months (defined as fr
188 dysfunction, it is critical to determine the patency of the transplant vasculature to guide clinical
189 hy, and ulnar frame count to investigate the patency of the ulnopalmar arches, as well as handgrip st
192 Primary end point was 6-month primary binary patency of treated lesions, defined as </=50% stenosis o
193 A follow-up after 12 and 24 months showed patency of treated vessels in 84% and 76% of patients, r
195 technical success and higher 1-year primary patency only if provisional stenting is considered targe
197 Morphologic parameters evaluated were IMA patency, origin of the IMA in relation to the aneurysm s
201 n important role in maintaining upper airway patency, particularly during sleep, and modulating upper
204 hronic obstructive pulmonary disease, airway patency problems, and prolonged mechanical ventilation.
205 hronic obstructive pulmonary disease; airway patency problems; or prolonged mechanical ventilation.
206 hways associated with neuromuscular junction patency (providing molecular evidence of sarcopenia-rela
208 imary aim of the trial is to compare (1) the patency rate (primary, primary assisted, and secondary p
212 elf-expanding nitinol stent has improved the patency rate of SFA after percutaneous transluminal angi
214 eved without surgical repair, with a carotid patency rate superior to published data after surgical c
216 TA, P=0.025 for superiority) and the primary patency rate was significantly higher with DCB (76.3% fo
217 ter-Society Consensus class D), the 12-month patency rate was significantly longer in VIA patients in
221 opliteal lesions, DES provide better 6-month patency rates and less amputations after 6 and 12 months
222 her the "best of both worlds": the excellent patency rates and survival benefits associated with the
226 rtery bypass graft surgery suffer from lower patency rates compared to left internal mammary artery.
229 ith thrombosis-free patency (thrombosis-free patency rates of 54%, 38%, and 26% for low, middle, and
230 nterior descending artery alongside the good patency rates of drug-eluting stents, which outlive saph
231 Off-pump CABG resulted in lower FitzGibbon A patency rates than on-pump CABG for arterial conduits (8
232 nstrated that it provides superior long-term patency rates to the saphenous vein in most situations.
234 mulative 1-, 2-, 3-, 5-, and 10-year primary patency rates were 64%, 59%, 54%, 45%, and 45%, respecti
236 me relevant secondary outcomes such as graft patency, rates of thrombosis, and interventions, other p
238 onal stent placement) and long-term (primary patency, repeat revascularization, major amputation, all
245 ent prolongation of primary unassisted graft patency that approached statistical significance (adjust
247 s were fractional flow reserve during vessel patency, the quantitative intracoronary ECG ST-segment e
248 a negative association with thrombosis-free patency (thrombosis-free patency rates of 54%, 38%, and
251 Blood contacting surfaces maintain their patency through physico-chemical properties of a functio
252 ee vaccinees (3/14, 21%), and delays time to patency through substantial reduction of liver-stage par
257 grafts had similar and acceptable long-term patency to support their use as a coronary artery bypass
259 of halofuginone dramatically increased lumen patency via adaptive remodeling and selective inhibition
261 - 1.8 months, the success rate of anatomical patency was 100% (27/27) and the success rate of symptom
264 ly (p = 0.0004); the median duration of SEMS patency was 24 w and 29 w for unilateral and bilateral p
269 (n=287 grafts including 9 sequential grafts) patency was 85% and right internal thoracic artery (n=15
275 tive anticoagulation was standard and venous patency was assessed by routine computed tomographic sca
276 iation of variables with the risk of loss of patency was assessed by using a Cox proportional hazards
280 red TTF and/or PI in 2738 grafts, and 1-year patency was determined in 1710 (62.5%) of these grafts.
283 US and fluoroscopic assessments of ureteral patency was evaluated by using a Clopper-Pearson exact b
288 d after 48 (11%) regular pDUS where arterial patency was questioned: 32 extra pDUS, 14 computed tomog
290 Immediate and long-term postoperative vein patency was similar to patients without hypercoagulabili
292 durations of the primary and secondary stent patency were 114.7+/-15.1 and 146.4+/-21.2 days, respect
294 cation rates and a superior cumulative stent patency when compared with PS placement in all Bismuth c
295 with DCB showed significantly higher primary patency when compared with PTA (78.9% vs. 50.1%; p < 0.0
296 iod, during which we analyzed hepatic artery patency with Doppler ultrasound at 1, 3, 6, and 12 month
298 isted patency, and 97% (85-98) had secondary patency, with most loss of primary patency because of th
300 ompared with portal veins, and only arterial patency within an ablation zone was related to local tum
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