ライフサイエンスコーパス: cadaveric renal transplant

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1 n Sharing status and LKT after failed OLT or cadaveric renal transplant.

2 nd subsequently received a successful second cadaveric renal transplant.

3 haplotype-identical LRDs, 379 SPKs, and 296 cadaveric renal transplants.

4 ion (DGF) and reduced graft survival (GS) of cadaveric renal transplants.

5 DGF) is frequently observed in recipients of cadaveric renal transplants.

6 ection, and graft survival in 37,216 primary cadaveric renal transplants (1985-1992).

7 aft failure rate in those patients receiving cadaveric renal transplants after a period of peritoneal

8 6363 primary cadaveric renal transplants carried out in 23 centres in

9 ients who were administered no induction and cadaveric renal transplant (CRT) recipients who were adm

10 idney survival results for 3642 SPK and 2374 cadaveric renal transplants (CRT) in type I diabetic pat

11 pediatric, 37 live donor adult, and 87 adult cadaveric renal transplants (CRT).

12 el, in 90 unsensitized recipients of primary cadaveric renal transplants (from a total of 1442 betwee

13 unction was significantly more common in the cadaveric renal transplant group.

14 D groups but was significantly lower for the cadaveric renal transplant group.

15 as significantly lower for recipients in the cadaveric renal transplant group.

16 13 highly sensitised patients underwent cadaveric renal transplants immediately after immunoadso

17 Eighteen patients underwent cadaveric renal transplant in the face of a historic IgG

18 Of a total of 78 cadaveric renal transplants in fiscal year 1995, there w

19 The cadaveric renal transplant median waiting time for non-A

20 from all diabetic patients receiving LRD or cadaveric renal transplants or SPKs from January 1986 th

21 yclosporine in preventing acute rejection in cadaveric renal transplant patients.

22 After cadaveric renal transplant, patients were randomized to

23 as merged to Medicare claims data for 42,868 cadaveric renal transplants performed between 1991-1996

24 We analyzed 786 consecutive primary cadaveric renal transplants performed by transplant cent

25 graft recipients to the level of our primary cadaveric renal transplant population.

26 A cadaveric renal transplant recipient given pretransplant

27 This effect is dominant enough that a cadaveric renal transplant recipient with an ESRD time l

28 risk factors for DGF in adult (age >/=16 yr) cadaveric renal transplant recipients by means of a mult

29 Graft survival in 163 cadaveric renal transplant recipients for whom molecular

30 rical cohort study was conducted of US adult cadaveric renal transplant recipients from January 1, 19

31 Network for Organ Sharing data of all adult cadaveric renal transplant recipients receiving kidneys

32 ween January 2001 and January 2002, 58 adult cadaveric renal transplant recipients were randomized to

33 vival up to 3 years posttransplant for first cadaveric renal transplant recipients were stratified by

34 ative Thymoglobulin administration, in adult cadaveric renal transplant recipients, is associated wit

35 of Thymoglobulin induction therapy in adult cadaveric renal transplant recipients.

36 Adult cadaveric renal-transplant recipients who received trans

37 allograft survival, we studied 31,600 first cadaveric renal transplants that were functional on the

38 th end-stage renal disease registered on the cadaveric renal transplant waiting list between January

39 A cadaveric renal transplant was performed on a 63-year-ol

40 h 1997 for the care of recipients of a first cadaveric renal transplant were analyzed according to th

41 ent survival rates in diabetic recipients of cadaveric renal transplants were significantly lower tha

42 rds to identify those patients who underwent cadaveric renal transplant, with a historic IgG positive

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