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1 in waiting times persist for deceased donor kidney transplantation.
2 address geographic disparities in access to kidney transplantation.
3 derived, he proceeded to simultaneous liver-kidney transplantation.
4 ay contribute to disparities in living donor kidney transplantation.
5 r, often into older age, and commonly pursue kidney transplantation.
6 rding the type of CMV preventive strategy in kidney transplantation.
7 ma release assay to predict CMV infection in kidney transplantation.
8 ministration is unfeasible in deceased-donor kidney transplantation.
9 development of injury and cytoprotection in kidney transplantation.
10 t preservation fluid predictive of DGF after kidney transplantation.
11 , three of whom underwent simultaneous heart-kidney transplantation.
12 ism was intentionally induced at the time of kidney transplantation.
13 ng DSA monitoring may improve outcomes after kidney transplantation.
14 he T cell-mediated immune response following kidney transplantation.
15 tion of a dn DSA, 65.3 months (median) after kidney transplantation.
16 he incidence of delayed graft function after kidney transplantation.
17 th impaired long-term clinical outcome after kidney transplantation.
18 patients and in the allocation of organs for kidney transplantation.
19 associated with increased risk of DGF after kidney transplantation.
20 ly assess virus transmission in living-donor kidney transplantation.
21 eGFR, initiation of maintenance dialysis, or kidney transplantation.
22 clinical importance in intensive care and in kidney transplantation.
23 e value for delayed graft function following kidney transplantation.
24 as well as in the immunological response to kidney transplantation.
25 ading cause of morbidity and mortality after kidney transplantation.
26 ney disease (CKD) arose from observations in kidney transplantation.
27 KV) is a significant cause of nephropathy in kidney transplantation.
28 sure (eLAP), and mortality in candidates for kidney transplantation.
29 donors and recipients was a breakthrough in kidney transplantation.
30 can ancestry improves outcomes and safety in kidney transplantation.
31 ocioeconomic status (SES) and outcomes after kidney transplantation.
32 ction of a dnDSA, 65.3 months (median) after kidney transplantation.
33 r donor kidney quality and function in human kidney transplantation.
34 sitization, after desensitization, and after kidney transplantation.
35 asures, that improve long-term outcome after kidney transplantation.
36 ociated with a lower likelihood of accessing kidney transplantation.
37 ropriate to refer an affected individual for kidney transplantation.
38 atients were excluded from consideration for kidney transplantation.
39 clinical trials of Treg therapy in liver and kidney transplantation.
40 cies that attempt to maximize survival after kidney transplantation.
41 etter understanding of racial disparities in kidney transplantation.
42 tized patients an opportunity for successful kidney transplantation.
43 disease with a high rate of recurrence after kidney transplantation.
44 8-year-old boy with previous living-related kidney transplantation.
45 anocytic squamous cell carcinoma (SCC) after kidney transplantation.
46 verity of infections in the first year after kidney transplantation.
47 l gastrectomy was evaluated for living donor kidney transplantation.
48 hort of 538 patients in the first year after kidney transplantation.
49 kidney transplantation who received a second kidney transplantation.
50 adverse cardiovascular outcomes in pediatric kidney transplantation.
51 ing these core outcome domains for trials in kidney transplantation.
52 iated with increased risk of mortality after kidney transplantation.
53 lume, VA centers offer excellent outcomes in kidney transplantation.
54 tation of core outcome domains for trials in kidney transplantation.
55 nt cause of loss of allograft function after kidney transplantation.
56 ed protein 4 Ig) is an emerging treatment in kidney transplantation.
57 ht induce cross-dressing following liver and kidney transplantation.
58 titative assessment of microperfusion during kidney transplantation.
59 function in donation after circulatory death kidney transplantation.
60 d as a reason for organ refusal in pediatric kidney transplantation.
61 de novo donor-specific antibody (DSA) after kidney transplantation.
62 infection-related morbidity and mortality in kidney transplantation.
63 ng, we applied this novel technique to human kidney transplantation.
64 sociated with higher risk of mortality after kidney transplantation.
65 ling solution to improve equity in access to kidney transplantation.
66 ted with inferior posttransplant outcomes in kidney transplantation.
67 ies in CKD are reversible and normalize with kidney transplantation.
68 potentially improve CMV-related outcomes in kidney transplantation.
69 easures that improve long-term outcome after kidney transplantation.
70 sure (eLAP), and mortality in candidates for kidney transplantation.
71 invasively detect acute rejection (AR) after kidney transplantation.
72 on, graft rejection, and graft failure after kidney transplantation.
73 ciency and pharmacotherapy initiation before kidney transplantation.
74 reduce disparities and equilibrate access to kidney transplantation.
75 a risk factor for acute kidney injury after kidney transplantation.
76 However, little data are available on kidney transplantation.
77 ible approach to treat DGF in deceased donor kidney transplantation.
78 15 to October 2018, included 128 consecutive kidney transplantations.
79 aiting list was 0.54% (95% CI 0.40-0.67) for kidney transplantation, 0.49% (0.36-0.62) for heart, 0.1
80 n within a 2-year follow-up was higher after kidney transplantation (20%) than in KTCs (5.5%) (P = .0
83 equired reconstruction more often with right kidney transplantation (72.5% vs 27.5%, P < .001), and t
84 splantation was 93.5% (95% CI 81.0-97.9) for kidney transplantation, 80.6% (63.6-90.3) for heart, 27.
85 > 80%, DSA+ = 50 versus DSA- = 40) received kidney transplantation after DES with IVIG + rituximab +
86 ADPKD) than by lower rates of deceased donor kidney transplantation after waitlisting (rates were onl
87 stenosis are often considered ineligible for kidney transplantation, although kidney transplantation
88 -related nephrotoxicity, and developments in kidney transplantation among HIV-positive individuals.
89 oss is a primary endpoint in many studies in kidney transplantation and a broad spectrum of risk fact
91 e present the first reported experience with kidney transplantation and donation in transgender patie
92 eports of the application of NMP in clinical kidney transplantation and each uses different approach
93 inhibitors (PPIs) are frequently used after kidney transplantation and have been associated with inc
94 lain racial/ethnic disparities in receipt of kidney transplantation and may mask the actual magnitude
95 rt to follow up LTBI status in patients with kidney transplantation and shows its higher prevalence a
101 nal tolerance has been achieved in liver and kidney transplantation, and some intestinal transplant p
102 cardinal causes of late allograft loss after kidney transplantation, and there is great need for noni
103 who had CKD stage 5 at presentation received kidney transplantation; and 1 patient required further h
104 The maternofetal outcomes in patients with kidney transplantation are comparable with those of nont
110 fied critically important outcome domains in kidney transplantation based on the shared priorities of
111 -inhibitor free immunosuppressive therapy in kidney transplantation but is associated with a higher a
113 ds effectively combats acute rejection after kidney transplantation, but at the cost of substantial s
114 important in clinical decision-making around kidney transplantation, but is difficult using available
115 Tac) is an effective anti-rejection agent in kidney transplantation, but its off-target effects make
119 ipients (SRTR) data to identify 92 081 adult kidney transplantation candidates who were offered a DCD
120 f glomerulonephritis that often recurs after kidney transplantation causing severe graft injury and o
122 nosuppressive regimen for combined islet and kidney transplantation (CIKTx) in nonhuman primates.
126 ) and Hispanic patients have lower access to kidney transplantation compared to non-Hispanic whites (
127 e to antibody-mediated rejection (AMR) after kidney transplantation, compared to one desensitized ani
128 a donation after circulatory death model of kidney transplantation comparing standard cold storage w
130 t maintenance immunosuppression regimens for kidney transplantation, concerns about toxicity have mad
131 s) (95% confidence intervals [CI]) for first kidney transplantation, controlling for year, demographi
132 n the field of viral hepatitis and liver and kidney transplantation convened a meeting to review curr
133 hnic minorities have lower rates of deceased kidney transplantation (DDKT) and living donor kidney tr
135 d racial and sex disparities in living donor kidney transplantation do not appear to be related to ne
141 sEVs released shortly after liver, but not kidney, transplantation exhibit immunoinhibitory effects
142 tigen-matched, sibling donor bone marrow and kidney transplantation for ESRD due to multiple myeloma.
143 trategies involving combined bone marrow and kidney transplantation for patients with and without an
144 Disparities that affect equity in access to kidney transplantation for patients with kidney failure
146 d enrolled 63 patients, of whom 30 underwent kidney transplantation from an HCV-viremic deceased dono
147 tal-body irradiation, underwent combined HCT/kidney transplantation from haploidentical donors; graft
148 neered simultaneous hematopoietic cell (HCT)/kidney transplantation from HLA-identical related donors
149 eactive antibody (cPRA) >=50% that underwent kidney transplantation from June 2013 to December 2016 i
150 s with a baseline cPRA >= 50% that underwent kidney transplantation from June 2013 to December 2016 i
154 in consideration the possibility of a living-kidney transplantation, had experienced persistent micro
155 in consideration the possibility of a living-kidney transplantation, had experienced persistent micro
157 ligible for kidney transplantation, although kidney transplantation has been acknowledged as the best
158 the incidence of cardiovascular events after kidney transplantation has changed from 1994 to 2009.
160 redict poorer 2-year survival outcomes after kidney transplantation have been identified in this larg
162 ge renal disease who require dialysis and/or kidney transplantation, have some of the highest rates o
164 zation has enabled incompatible living donor kidney transplantation (ILDKT) across HLA/ABO barriers,
165 unosuppression and underimmunosuppression in kidney transplantation, impacting short- and long-term o
167 NT-proBNP on arrival at the hospital before kidney transplantation in 658 KTR between January 1995 a
168 day -7 (n = 4, group C) before living donor kidney transplantation in addition to post-transplantati
169 cts of HOPE on the immune response following kidney transplantation in an allogeneic rodent model.
170 aim of this study was to examine outcomes of kidney transplantation in APRT deficiency patients.
171 site for dialysis-treated patients to access kidney transplantation in Canada, is a subjective proces
177 the circulation shortly after liver, but not kidney, transplantation in association with the release
178 assing a spectrum of renal dysfunction after kidney transplantation including those who may or may no
180 mmalian target of rapamycin inhibitors after kidney transplantation is associated with a concentratio
181 segmental glomerular sclerosis (FSGS) after kidney transplantation is challenging with unpredictable
184 alovirus (CMV) immune-risk stratification in kidney transplantation is highly needed to establish gui
185 mediated rejection (ABMR) classification for kidney transplantation is interpreted in practice and af
190 usion until transplant: 69 with simultaneous kidney transplantation (KT) (at time of LT, group 1) and
193 with end-stage renal disease is longer after kidney transplantation (KT) compared with those remainin
194 African Americans (AA) have lower rates of kidney transplantation (KT) compared with Whites (WH), e
195 The old-for-old allocation policy used for kidney transplantation (KT) has confirmed the survival b
196 mmalian target of rapamycin inhibitors after kidney transplantation (KT) have not been fully addresse
197 tandard of care immunosuppressive regimen in kidney transplantation (KT) includes a combination of my
205 Subclinical rejection (SCR) screening in kidney transplantation (KT) using protocol biopsies and
206 needed to monitor stable patients following kidney transplantation (KT), as subclinical rejection, c
207 to understand the impact of the epidemic on kidney transplantation (KT), at both the national and ce
208 actors for invasive aspergillosis (IA) after kidney transplantation (KT), we conducted a systematic s
212 onveterans, the impact of rurality status on kidney transplantation (KTP) access among veterans is un
213 e of BK polyomavirus (BKPyV) infection after kidney transplantation (KTx), including development of B
215 dney transplantation (DDKT) and living donor kidney transplantation (LDKT) in the United States.
216 he presence of sex disparity in living donor kidney transplantation (LDKT) remains controversial.
217 sought to assess likelihood of living donor kidney transplantation (LDKT) within a single-center kid
218 ociated with worse outcomes after live donor kidney transplantation (LDKT), and prior work suggests t
219 dress patient-level barriers to living-donor kidney transplantation (LDKT), centers have implemented
223 g these brain abnormalities before and after kidney transplantation may identify potential reversibil
224 sponses and graft pathology, we used a mouse kidney transplantation model that subjected MHC-mismatch
227 ents of the United States who are in need of kidney transplantation occasionally contract with living
229 importance of outcome domains for trials in kidney transplantation on a 9-point Likert scale and pro
230 erial spin labeling to assess the effects of kidney transplantation on cerebral blood flow and magnet
232 ienced progressive CKD (defined as dialysis, kidney transplantation, or a 40% decline from postnephre
233 e (defined as dialysis for at least 90 days, kidney transplantation, or confirmed sustained eGFR <15m
234 r >=90 days, chronic dialysis for >=90 days, kidney transplantation, or death from kidney failure) in
235 history of pretransplant melanoma, previous kidney transplantation, or transplantation after 2012 or
238 titutes of Health-sponsored "APOL1 Long-term Kidney Transplantation Outcomes" Network will determine
244 phic disparities in access to deceased donor kidney transplantation persist in the United States unde
245 n the adjusted probability of deceased donor kidney transplantation persist under KAS, even between c
246 aphics, comorbidities, dialysis vintage, and kidney transplantation, PH was associated with twice the
247 raphics, comorbidities, dialysis vintage and kidney transplantation, PH was associated with twice the
248 ith adverse patient and graft outcomes after kidney transplantation, pilot data suggest that PH may i
249 lude that, in this nonhuman primate model of kidney transplantation, PRCL-02 demonstrated evidence of
250 liver transplantation or combined liver and kidney transplantation prior to the visit revealing a wi
251 , blood group, renal replacement time, prior kidney transplantation, race, gender, diabetes, and tran
254 es for all clinical stakeholders to increase kidney transplantation rates, and reduce total costs of
255 lysis facilities have historically had lower kidney transplantation rates, but it is unknown if the p
256 use a large cohort of Veterans Affairs (VA) kidney transplantation recipients to assess the risk of
257 own encouraging results for the treatment of kidney transplantation recipients with focal segmental g
258 of transplantation in 19 450 deceased donor kidney transplantation recipients with Medicare as prima
260 CKD, liver retransplantation associated with kidney transplantation (ReLT-KT) might be necessary.
265 disease leads to a growing waiting list for kidney transplantation resulting from the scarcity of ki
266 zation in pediatric blood group incompatible kidney transplantation results in excellent outcomes wit
267 une responses, clinical use of belatacept in kidney transplantation revealed a substantially high inc
268 uture efforts aimed to improve outcome after kidney transplantation should align with the relative we
270 mented, the proportion of simultaneous liver-kidney transplantation (SLKT) has increased significantl
275 national Standardized Outcomes in Nephrology-Kidney Transplantation stakeholder consensus workshops i
277 s a leading cause of allograft failure after kidney transplantation, the cellular and molecular proce
278 e countries, thus enabling them to receive a kidney transplantation they otherwise could not afford.
279 are new trials in autoimmunity and heart and kidney transplantation to determine effectiveness of inh
280 ildren were randomized at 4 to 6 weeks after kidney transplantation to switch to everolimus with redu
283 dren with steroid-resistant NS who underwent kidney transplantation using next-generation sequencing.
284 luation processes to determine candidacy for kidney transplantation, variability in graft failure exi
285 rn holds for living donor and deceased donor kidney transplantation, varies by facility ownership, or
286 dialysis to placement on the deceased donor kidney transplantation waiting list, receipt of a living
289 requent, some restrictions to deceased donor kidney transplantation were reported by 84.0% and deceas
291 HD occurring in recipients of pancreas after kidney transplantation, which were diagnosed at 5.5 and
293 squamous cell carcinoma (SCC) after a first kidney transplantation who received a second kidney tran
295 (NSAID) use is recommended to be avoided in kidney transplantation, with a paucity of studies assess
296 mulative percentage of patients referred for kidney transplantation within 1 year of dialysis at the
297 calculated the probability of deceased donor kidney transplantation within 3 years of wait listing us
298 chronic dialysis) and listing or receipt of kidney transplantation within 5 years was examined in in
299 se patients and allowed them to benefit from kidney transplantation without an increased risk of oppo
300 e agent mycophenolate is used extensively in kidney transplantation, yet dosing strategy applied vari