ライフサイエンスコーパス: intrapericardial

コーパス検索結果 (１語後でソート)

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1 VAT (-22%), intrahepatic (-29%), and intrapericardial (-11%) fats declines were higher than p

2 With x-ray/MR imaging, successful intrapericardial access and delivery were achieved in al

3 Intrapericardial administration allows investigation of

4 age, hypertrophied animals were treated with intrapericardial administration of recombinant VEGF prot

5 nt and fifty percent of neurons responded to intrapericardial algogenic chemicals (0.2 ml) in male an

6 We compared the effects of intrapericardial and intracoronary nitroglycerin on coro

7 the low-fat diet in decreasing intrahepatic, intrapericardial, and pancreatic fats (P<0.05 for all).

8 Intrapericardial bradykinin (IB) altered activity of 58/

9 The number of cuneate neurons responding to intrapericardial bradykinin (IB, 15.6%, 17/109) was sign

10 We compared a newer LVAD design (a small intrapericardial centrifugal-flow device) against existi

11 eligible for heart transplantation, a small, intrapericardial, centrifugal-flow LVAD was found to be

12 /311 (31%) neurons responded to both TED and intrapericardial chemicals (IC) and 48/177 (27%) neurons

13 f 55 (27%) superficial neurons responsive to intrapericardial chemicals were compared to 80/169 (47%)

14 nd for 77/95 (81%) neurons that responded to intrapericardial chemicals.

15 ular exposure of coronary arteries to NO via intrapericardial D-BSA administration reduced flow-restr

16 Ablation was limited by intrapericardial defibrillator patches adherent to the l

17 With x-ray/MR imaging guidance, intrapericardial delivery can be performed safely in the

18 Intrapericardial delivery of angiogenic factors may offe

19 Intrapericardial delivery of BaCaps with hMSCs leads to

20 d coronary vasodilation can be achieved with intrapericardial delivery of nitroglycerin without syste

21 The data suggest that intrapericardial delivery of NO donors for which NO rele

22 onatal mice (age, 2 days; n = 131) underwent intrapericardial delivery of recombinant adenoviruses en

23 imaging 1 week after x-ray/MR imaging-guided intrapericardial delivery showed no evidence of pericard

24 obilization are sparse.We sought to evaluate intrapericardial-fat (IPF) and extrapericardial-fat (EPF

25 Intrapericardial injection of D-BSA immediately before 3

26 creased in six out of six neurons excited by intrapericardial injections.

27 s with steroids (13.2%, 10.0%, and 29.4% for intrapericardial, intravenous or oral, and none, respect

28 G with steroids (36.8%, 30.0%, and 41.2% for intrapericardial, intravenous or oral, and none, respect

29 Catheter-based intrapericardial (IPC) delivery of therapeutic agents ha

30 nd histopathology of a percutaneously placed intrapericardial lead (IPL).

31 Intrapericardial nitroglycerin (200 microg) was administ

32 e investigated the antiarrhythmic effects of intrapericardial nitroglycerin (NTG) during acute myocar

33 Intrapericardial nitroglycerin was associated with a mea

34 ved at 3 min with intracoronary but not with intrapericardial nitroglycerin.

35 icular pressure by dobutamine was blunted by intrapericardial NTG (from 3,999 +/- 196 mm Hg/s before

36 Intrapericardial NTG exerts a robust antifibrillatory ac

37 Intrapericardial NTG suppressed VF at 45 min in all six

38 ctions in pump size, centrifugal design, and intrapericardial positioning may reduce complications an

39 ompliance, which are exacerbated by elevated intrapericardial pressure.

40 are more effective when administered by the intrapericardial rather than intravascular route.

41 eparations, the device was inserted into the intrapericardial space through a subxiphoid approach.

42 last 38 procedures (44.7%) were followed by intrapericardial steroid injection.

43 itic chest pain was significantly reduced by intrapericardial steroids (58.8% versus 21.1%; P=0.006)

44 tic chest pain is significantly decreased by intrapericardial steroids.

45 sed for c-fos immunohistochemistry following intrapericardial stimulation with mechanical, chemical,

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