ライフサイエンスコーパス: peripheral vein

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

2 to continuously collect CTCs directly from a peripheral vein.

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

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

5 93 and 1998 who received Atgam induction via peripheral vein.

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

7 preeminent even when insulin is given into a peripheral vein.

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

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

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

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

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

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

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

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

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

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

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

19 7 proteins that significantly changed in the peripheral vein blood after PMI in a derivation cohort (

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

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

22 The pre-labelled MSCs were administrated via peripheral vein in a mouse (n = 1), rats (n = 4), rabbit

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

24 Peripheral vein infusion is safe, convenient, and econom

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

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

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

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

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

30 sertion) during caesarean section and from a peripheral vein on the same day and second day post-part

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

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

33 After MSC administration via peripheral vein, PET imaging revealed intense radiotrace

34 Bile acid levels decrease in the peripheral vein post-TIPS, and the abundances of three s

35 g hepatic vein (HV), peripheral artery (PA), peripheral vein (PV) and portal vein (PoV) using single-

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

37 Six sets of adrenal vein and peripheral vein samples were obtained: three baseline sa

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

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

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

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

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

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

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

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

46 evels were higher in the uterine than in the peripheral vein with a median difference of 52.2 (IQR 20

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