ライフサイエンスコーパス: platelet concentrate

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1 y reduced by preabsorption with pooled human platelet concentrate.

2 levels of GF suggested to be associated with platelet concentrate.

3 nological functions of leukocytes present in platelet concentrates.

4 g viruses, bacteria, and leukocytes in human platelet concentrates.

5 eloped to inactivate bacteria and viruses in platelet concentrates.

6 atter requires transfusion of HLA-compatible platelet concentrates.

7 telet-rich fibrin (PRF), a second-generation platelet concentrate, and atorvastatin (ATV), a potent m

8 PLA2 was measured in packed red blood cells, platelet concentrates, and fresh frozen plasma over the

9 tokines in the plasma fraction of transfused platelet concentrates, and leukodepletion prior to stora

10 powerful marker to determine the quality of platelet concentrates, because it reflects metalloprotei

11 study, it can be concluded that PRF and PRGF platelet concentrate failed to augment clinical effects

12 nt feasibility of using UVB-irradiated human platelet concentrates for prevention of HLA alloimmuniza

13 ns were found in transfused patients, pooled platelet concentrates, fresh frozen plasma, and packed r

14 A platelet concentrate graft (PCG) was applied underneath

15 The platelet concentrate graft may be an alternative graft m

16 rial were to assess the clinical efficacy of platelet concentrate grafts (PCG) in the treatment of Mi

17 anufacture of buffy coat whole-blood-derived platelet concentrate have convinced the Canadian Blood S

18 Platelet-rich fibrin (PRF) is a platelet concentrate having sustained release of various

19 Storage of platelet concentrates, however, is associated with a red

20 The topical use of platelet concentrates is recent, and its efficiency rema

21 eloped countries, bacterial contamination of platelet concentrates is the highest infectious risk in

22 Platelet concentrates may be prepared from whole blood o

23 Platelet concentrates (p = .004) were transfused less in

24 Platelet concentrate (PC) is known to contain growth fac

25 Both platelet concentrates (PC) derived from whole blood or s

26 40L were measured in blood components and in platelet concentrates (PCs) implicated in TRALI or contr

27 ve therapy for furcation defects, the use of platelet concentrates (PCs) in addition to open flap deb

28 hemorrhagic complications, administration of platelet concentrates, plasma, or coagulation factor con

29 or limitation, however, was the finding that platelet concentrates prepared from blood anticoagulated

30 In addition, platelet concentrates prepared from F-LR + MPR whole blo

31 gatively affect availability and activity of platelet concentrate-suggested growth factors (GF).

32 ferentiation after treatment with TGFbeta or platelet concentrate supernatant, assessed by alpha smoo

33 let-rich fibrin (PRF) is a second-generation platelet concentrate that releases various growth factor

34 sfusion of 2 fresh ABO blood group-identical platelet concentrates (therapeutic units), ongoing plate

35 Previous studies have shown that exposure of platelet concentrates to riboflavin and light (Mirasol P

36 Extracellular mitochondria are found in platelet concentrates used for transfusion and are prese

37 he detection of a bacterial contamination of platelet concentrates was assessed using samples spiked

38 crease with filter A after the first 5 mL of platelet concentrates was filtered that returned to pref

39 One hundred sixty-six of these platelet concentrates were then transfused to 120 patien

40 randomized to receive prophylactic apheresis platelet concentrates when the platelet count was either

41 ed by PCFIA, occurs during leukodepletion of platelet concentrates with either filter A or B.

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