ライフサイエンスコーパス: peripheral vein

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1 ere safely administered to the patient via a peripheral vein.

2 rtal vein, hepatic vein, and an arterialized peripheral vein.

3 usion was switched from the portal vein to a peripheral vein.

4 93 and 1998 who received Atgam induction via peripheral vein.

5 administered into the portal vein or into a peripheral vein.

6 d drawn from the internal jugular vein and a peripheral vein.

7 asured vitamin C and cortisol in adrenal and peripheral veins.

8 njected with repeated doses of ADHLSCs via a peripheral vein (35 million In-oxine-labeled cells, foll

9 with preexisting immunity to AAV8 following peripheral vein administration of 1x10(12) vg/kg AAV5-ps

10 Within 48 hours after peripheral vein administration of the vector to FVIII-de

11 matic VTE (two involving the deep veins, one peripheral vein and one pulmonary embolism).

12 l procedures included US localization of the peripheral vein and postprocedural chest radiograph to a

13 of exercise, somatostatin was infused into a peripheral vein, and insulin and glucagon were infused i

14 portal vein (4 mg x kg(-1) x min(-1)) and a peripheral vein, as needed, to maintain arterial plasma

15 energic agonist dobutamine was infused via a peripheral vein before and during concurrent intracorona

16 ial blood sampling of the coronary sinus and peripheral vein before, during, and after infusion allow

17 7 proteins that significantly changed in the peripheral vein blood after PMI in a derivation cohort (

18 ive simultaneous central venous catheter and peripheral vein blood cultures were included.

19 erventions, such as coronary angioplasty and peripheral vein grafting.

20 X (FIX) transgene (scAAV2/8-LP1-hFIXco) in a peripheral vein in six patients with severe hemophilia B

21 Peripheral vein infusion is safe, convenient, and econom

22 Peripheral vein infusion of 1x10(12) vg/kg scAAV-LP1-hFI

23 Equine ATG can be safely administered via peripheral vein infusion.

24 Peripheral-vein infusion of scAAV2/8-LP1-hFIXco resulted

25 In adult macaques, a single peripheral vein injection of 2 x 10(11) vg/kg of the hFV

26 an ultrasound contrast agent injected into a peripheral vein is accelerated in patients with cirrhosi

27 ence of thrombotic events in visceral and/or peripheral veins or arteries (HR 7.66, 95% CI 2.13-27.51

28 Pulmonary vein (PV) and peripheral vein (Pe) blood specimens from patients with

29 The jugular vein/peripheral vein ratio was 1.4 in patients with MS vs. 1.

30 drawn through either the central catheter or peripheral vein shows excellent negative predictive valu

31 e safely administered equine ATG (Atgam) via peripheral veins since 1978.

32 res from the central venous catheter and the peripheral vein to become positive, as well as other rel

33 a fourfold basal rate (PoI, n = 6), or via a peripheral vein to create a selective increase in the ar

34 Glucose was infused through a peripheral vein to create hyperglycemia (12.5 mmol/l pla

35 omol/L at 1-4 min, whereas the corresponding peripheral vein vitamin C concentrations were 35 +/- 15

36 e stimulation increases adrenal vein but not peripheral vein vitamin C concentrations.

37 normal saline during 20 to 30 minutes into a peripheral vein with a high-pressure bag.

38 tures should be performed, preferably from a peripheral vein, without interval between samples to avo

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