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1 imilar with TacHexal and Prograf early after kidney transplantation.
2 on may be appropriate for all patients after kidney transplantation.
3 ct on HO-1 upregulation after deceased donor kidney transplantation.
4 cies that attempt to maximize survival after kidney transplantation.
5 d has a high propensity for recurrence after kidney transplantation.
6 s well as competition in improving access to kidney transplantation.
7 ising preconditioning strategies before ABOi kidney transplantation.
8 r reason for late allograft loss in clinical kidney transplantation.
9 of patients with AA nephropathy (AAN) after kidney transplantation.
10 usal chain surrounding racial disparities in kidney transplantation.
11 etter understanding of racial disparities in kidney transplantation.
12 esent a surgical challenge in the context of kidney transplantation.
13 - and 3-year mortality among dialysis versus kidney transplantation.
14 ss of kidney function requiring dialysis and kidney transplantation.
15 on with market competition in the conduct of kidney transplantation.
16 ney perfusion (NEVKP) in heart-beating donor kidney transplantation.
17 osis remains an important complication after kidney transplantation.
18 tized patients an opportunity for successful kidney transplantation.
19 rsistent hyperparathyroidism is common after kidney transplantation.
20 ograft may help realize the full benefits of kidney transplantation.
21 ith the compounding issues of CKD, ESRD, and kidney transplantation.
22 that decrease long-term graft survival after kidney transplantation.
23 ir suppressive function predictive of AKI in kidney transplantation.
24 lead to the recurrence of proteinuria after kidney transplantation.
25 be a potential intervention also in clinical kidney transplantation.
26 rt-term patient and allograft survival after kidney transplantation.
27 s were followed up from 1 to 36 months after kidney transplantation.
28 hange estimated racial/ethnic disparities in kidney transplantation.
29 uency of secondary hyperparathyroidism after kidney transplantation.
30 with an increased acute rejection rate after kidney transplantation.
31 herapeutic targets for improving outcomes of kidney transplantation.
32 arding the effect of stopping smoking before kidney transplantation.
33 ay to predict the long-term outcome of human kidney transplantation.
34 disease with a high rate of recurrence after kidney transplantation.
35 evel greater than 200 mumol/L at day 7 after kidney transplantation.
36 most concerned with the financial burden of kidney transplantation.
37 tched nondonors who underwent deceased donor kidney transplantation.
38 ffect social participation in patients after kidney transplantation.
39 sease about all treatment options, including kidney transplantation.
40 (n = 2) underwent full MHC-mismatched heart/kidney transplantation.
41 sfunction influences candidate selection for kidney transplantation.
42 in pathway on long-term graft survival after kidney transplantation.
43 o list for and receipt of simultaneous liver kidney transplantation.
44 s used as a criterion for simultaneous liver-kidney transplantation.
45 end-stage renal disease and recurrence after kidney transplantation.
46 oadsorption column reuse in ABO-incompatible kidney transplantation.
47 oes not improve delayed graft function after kidney transplantation.
48 ications of prescription narcotic use before kidney transplantation.
49 aking decisions regarding simultaneous liver-kidney transplantation.
50 Proteinuria occurs commonly after kidney transplantation.
51 med, with 4 of the 27 including simultaneous kidney transplantation.
52 se patients with ESRD have limited access to kidney transplantation.
53 8-year-old boy with previous living-related kidney transplantation.
54 total of 27 HIV-positive patients underwent kidney transplantation.
55 , no relevant literature exists on CRS after kidney transplantation.
56 ation, especially in patients considered for kidney transplantation.
57 patients on dialysis on the waiting list for kidney transplantation.
58 ir influence on the practice of living donor kidney transplantation.
59 o influence graft survival in deceased-donor kidney transplantation.
60 ter I/R injury of mice and in patients after kidney transplantation.
61 hrologists' attitudes to patients' access to kidney transplantation.
62 anocytic squamous cell carcinoma (SCC) after kidney transplantation.
63 verity of infections in the first year after kidney transplantation.
64 l gastrectomy was evaluated for living donor kidney transplantation.
65 hort of 538 patients in the first year after kidney transplantation.
66 kidney transplantation who received a second kidney transplantation.
67 adverse cardiovascular outcomes in pediatric kidney transplantation.
68 ing these core outcome domains for trials in kidney transplantation.
69 atients were excluded from consideration for kidney transplantation.
70 iated with increased risk of mortality after kidney transplantation.
71 tation of core outcome domains for trials in kidney transplantation.
72 nt cause of loss of allograft function after kidney transplantation.
73 ed protein 4 Ig) is an emerging treatment in kidney transplantation.
74 ies against mismatched donor HLA antigens in kidney transplantation.
75 clinical trials of Treg therapy in liver and kidney transplantation.
76 trolled NEVKP improves renal function in DCD kidney transplantation.
77 sed safely and effectively in patients after kidney transplantation.
78 e the consistency and relevance of trials in kidney transplantation.
79 ecision was to submit the patient to a liver-kidney transplantation.
80 a scenario that is common in bone marrow and kidney transplantation.
81 were three main subgroups: 18 patients after kidney transplantation, 10 patients with gastrointestina
82 tudy period, there were 385,498 listings for kidney transplantation, 252 of which were prior donors.
84 ADPKD) than by lower rates of deceased donor kidney transplantation after waitlisting (rates were onl
86 val advantage for SPK recipients compared to kidney transplantation alone (KTA) is controversial.
87 ion treated with IIT and to 13 patients with kidney transplantation alone or simultaneous pancreas-ki
88 -related nephrotoxicity, and developments in kidney transplantation among HIV-positive individuals.
89 ur understanding of fracture incidence after kidney transplantation and how it compares to nontranspl
90 aimed to evaluate antibiotic prophylaxis in kidney transplantation and identify risk factors for SSI
92 frequent in immunosuppressed patients after kidney transplantation and may lead to allograft failure
93 l cytotoxic CD4(+) CD28(null) cell subset in kidney transplantation and points to strategies that may
94 ng clinical trial data on acute rejection in kidney transplantation and response to Infliximab in ulc
95 antibody (dnDSA) during the first year after kidney transplantation and the impact of early dnDSA on
96 term immunosuppressive drug treatment due to kidney transplantation and the second case is a malignan
97 d on historical practice patterns related to kidney transplantation and were never designed to minimi
98 cardinal causes of late allograft loss after kidney transplantation, and there is great need for noni
99 who had CKD stage 5 at presentation received kidney transplantation; and 1 patient required further h
100 nderwent haploidentical MHC-mismatched heart/kidney transplantation; and group 4 (n = 2) underwent fu
101 on SSIs were deceased donor, thin ureters at kidney transplantation, antithymocyte globulin induction
102 recurrence rate of AAGN within 5 years after kidney transplantation appeared slightly higher than in
103 The maternofetal outcomes in patients with kidney transplantation are comparable with those of nont
108 tive liver transplantations and living-donor kidney transplantations are also now on the horizon.
109 sease (ESRD) patients are not educated about kidney transplantation as a treatment option at the time
110 urine output at days 1, 7, 15, and 30 after kidney transplantation as well as at hospital discharge.
112 fied critically important outcome domains in kidney transplantation based on the shared priorities of
113 pation in patients 3 months to 6 years after kidney transplantation (baseline) and their impact on gr
115 ated in 240 patients who were waitlisted for kidney transplantation between 2008 and 2010, and patien
117 -inhibitor free immunosuppressive therapy in kidney transplantation but is associated with a higher a
119 with antibody-mediated rejection (AMR) after kidney transplantation by rituximab and plasmapheresis i
120 cular risk factor assessment in selection of kidney transplantation candidates for cardiac evaluation
122 issing in-hospital mortality, admission post kidney transplantation, chronic renal replacement therap
124 on of endogenous stem cells immediately post kidney transplantation combined with repeat therapy at 1
126 ion in the Reducing Disparities in Access to kidNey Transplantation Community Study (RaDIANT), a rand
127 Despite a significant survival advantage of kidney transplantation compared with dialysis, nearly on
128 antly worse graft and patient outcomes after kidney transplantation compared with nonindigenous Austr
130 t maintenance immunosuppression regimens for kidney transplantation, concerns about toxicity have mad
131 an aTreg percentage higher than 1.46% before kidney transplantation conferred an increased risk of AR
133 trategies to improve graft outcome following kidney transplantation consider information at the human
134 s) (95% confidence intervals [CI]) for first kidney transplantation, controlling for year, demographi
136 ents and increasing access to deceased donor kidney transplantation (DDKT) for highly sensitized pati
138 Patients in the United States waiting for kidney transplantation die in increasing numbers owing t
141 al study involving 95 children who underwent kidney transplantation due to NS, excluding congenital c
144 esity among children starting RRT may impede kidney transplantation, especially from living donors.
146 ining bone marrow transplantation (BMT) with kidney transplantation following non-myeloablative condi
148 llosensitization in two recipients following kidney transplantation from a highly sensitized donor.
151 tudy demonstrates that despite the fact that kidney transplantation from elderly deceased donors is a
155 group 1 (n = 3) underwent class I-mismatched kidney transplantation; group 2 (n = 3) underwent 2 sequ
156 3) underwent 2 sequential class I-mismatched kidney transplantations; group 3 (n = 2) underwent haplo
160 the incidence of cardiovascular events after kidney transplantation has changed from 1994 to 2009.
163 rategies to improve allograft survival after kidney transplantation have been directed to recipient-d
166 dinal follow-up of eight children undergoing kidney transplantation, HDL-induced production of endoth
167 ality of life (HRQOL) usually improved after kidney transplantation; however, a non-negligible number
168 h an increased morbidity and mortality after kidney transplantation; however, their clinical utility
169 multaneous islet-kidney (SIK) or islet-after-kidney transplantation (IAK) are rare and have never bee
170 desensitization and incompatible live donor kidney transplantation (ILDKT) constitute a unique subpo
175 plant BMI on the risk of graft failure after kidney transplantation in both unadjusted and adjusted m
176 ducted a prospective, nonrandomized study of kidney transplantation in HIV-infected patients who had
183 ents who started HHD with those who received kidney transplantation in the United States between 2007
185 pective trial including all ABO-incompatible kidney transplantations in Switzerland from 2005 to 2011
186 g of baseline serum creatinine, dialysis, or kidney transplantation) in the adjusted analyses (P<0.01
187 icentric Swiss protocol for ABO-incompatible kidney transplantation including immunoadsorption column
188 ced a national protocol for ABO-incompatible kidney transplantation including immunoadsorption column
189 assing a spectrum of renal dysfunction after kidney transplantation including those who may or may no
190 erence to immunosuppressive medication after kidney transplantation is a behavioral issue and as such
193 ng conditions, the need for midodrine before kidney transplantation is a risk marker for complication
195 mmalian target of rapamycin inhibitors after kidney transplantation is associated with a concentratio
198 epigenetic modifications on the outcomes of kidney transplantation is currently poorly understood an
206 usion until transplant: 69 with simultaneous kidney transplantation (KT) (at time of LT, group 1) and
207 ts reported in the literature that underwent kidney transplantation (KT) after a previous HSCT from t
208 ompleting the work-up (WU) and/or undergoing kidney transplantation (KT) but this has not been well d
209 The old-for-old allocation policy used for kidney transplantation (KT) has confirmed the survival b
213 s are affected by significant disparities in kidney transplantation (KT) in Veterans Affairs (VA) and
218 nsplant Research data, we compared access to kidney transplantation (KT), time from ESRD to listing,
222 in rates of preKT, focusing on living donor kidney transplantation (LDKT) and specifically recipient
223 he presence of sex disparity in living donor kidney transplantation (LDKT) remains controversial.
225 eceive disproportionately fewer living donor kidney transplantations (LDKTs) than non-Hispanic whites
227 We hypothesized that midodrine use before kidney transplantation may be a novel marker for posttra
230 ns for apparent disease-specific barriers to kidney transplantation might inform center-specific tran
233 importance of outcome domains for trials in kidney transplantation on a 9-point Likert scale and pro
234 econditioning therapies in living donor ABOi kidney transplantation on graft and patient outcomes.
236 history of pretransplant melanoma, previous kidney transplantation, or transplantation after 2012 or
243 ith adverse patient and graft outcomes after kidney transplantation, pilot data suggest that PH may i
245 rticosteroid withdrawal (CW) after pediatric kidney transplantation potentially improves growth while
246 igh levels of prescription opioid use before kidney transplantation predict increased risk of posttra
248 , blood group, renal replacement time, prior kidney transplantation, race, gender, diabetes, and tran
251 es for all clinical stakeholders to increase kidney transplantation rates, and reduce total costs of
254 own encouraging results for the treatment of kidney transplantation recipients with focal segmental g
255 of transplantation in 19 450 deceased donor kidney transplantation recipients with Medicare as prima
264 zation in pediatric blood group incompatible kidney transplantation results in excellent outcomes wit
266 t was best with the Rotterdam Comorbidity in Kidney Transplantation score compared to separate comorb
270 a therapy in patients on dialysis undergoing kidney transplantation should take into account the poss
271 viously described signatures of tolerance in kidney transplantation showing the differential expressi
272 ts who reach end-stage renal disease, single kidney transplantation (SKT) or combined kidney-pancreas
273 to determine the need for simultaneous liver kidney transplantation (SLK) versus liver alone transpla
275 alysis, pancreas after simultaneous pancreas-kidney transplantation/solitary pancreatic transplantati
276 ysis revealed that the risk factors for post-kidney transplantation SSIs were deceased donor, thin ur
277 unosuppression therapy, deceased donor, post-kidney transplantation SSIs, and delayed graft function.
278 national Standardized Outcomes in Nephrology-Kidney Transplantation stakeholder consensus workshops i
279 rge registry study comparing dialysis versus kidney transplantation survival outcomes of waitlisted a
280 n large registries, survival is longer after kidney transplantation than when remaining on dialysis.
282 0.31 to 0.93); with censoring of time after kidney transplantation, the relative hazard was 0.56 (95
286 eceased donors) and the risk of cancer after kidney transplantation using adjusted Cox proportional h
287 dren with steroid-resistant NS who underwent kidney transplantation using next-generation sequencing.
288 ibed the outcomes of adult living donor ABOi kidney transplantations using any form of preconditionin
293 Using a stringent mouse model of allogeneic kidney transplantation, we demonstrated that acute allog
295 ts chronic rejection changes in experimental kidney transplantation which indicates that sunitinib co
296 as do not properly reflect renal function in kidney transplantation, which makes their use in clinica
297 squamous cell carcinoma (SCC) after a first kidney transplantation who received a second kidney tran
299 T) and specifically recipients who underwent kidney transplantation within 1 year of initiating dialy
300 se patients and allowed them to benefit from kidney transplantation without an increased risk of oppo
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