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1 oons in patients undergoing femoro-popliteal percutaneous transluminal angioplasty.
2 was smaller in the medical group versus the percutaneous transluminal angioplasty and stenting (PTAS
3 roke that is increasingly being treated with percutaneous transluminal angioplasty and stenting (PTAS
5 and D lesions are not randomized and receive percutaneous transluminal angioplasty and stenting or fe
6 to receive either femoropopliteal bypass or percutaneous transluminal angioplasty and stenting; pati
9 porary studies (2005-2015) on the effects of percutaneous transluminal angioplasty for the treatment
13 treatment of peripheral artery disease with percutaneous transluminal angioplasty is limited by the
14 ctory angina pectoris when bypass surgery or percutaneous transluminal angioplasty is not indicated.
15 oved the likelihood of technical success for percutaneous transluminal angioplasty of dialysis access
17 f patients with critical limb ischemia using percutaneous transluminal angioplasty (PTA) and bail-out
18 l restenosis and reintervention rates versus percutaneous transluminal angioplasty (PTA) and improve
20 treatment with a low-dose DCB or an uncoated percutaneous transluminal angioplasty (PTA) balloon.
21 dy of mature accesses that underwent balloon percutaneous transluminal angioplasty (PTA) between Janu
22 el drug-eluting balloons versus conventional percutaneous transluminal angioplasty (PTA) for the redu
23 We compared a paclitaxel-coated balloon with percutaneous transluminal angioplasty (PTA) for the trea
24 eserved for lesions that are not amenable to percutaneous transluminal angioplasty (PTA) or for recur
25 runs were higher (all P<.001) than those for percutaneous transluminal angioplasty (PTA), as were rad
26 e 1-year outcomes compared with conventional percutaneous transluminal angioplasty (PTA), yet durabil
29 gned to DCB (n=200) or standard angioplasty (percutaneous transluminal angioplasty [PTA]) (n=100).
31 (2 with subclavian-carotid bypass and 5 with percutaneous transluminal angioplasty stenting of the su
32 , and reinterventions after femoro-popliteal percutaneous transluminal angioplasty up to 1 year of fo
33 o has successfully undergone angiography and percutaneous transluminal angioplasty using CO2 as the s
35 popliteal atherosclerotic disease undergoing percutaneous transluminal angioplasty were randomized to
36 c femoropopliteal peripheral artery disease, percutaneous transluminal angioplasty with a paclitaxel-
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