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1 ry at all US centers including our own (open kidney transplant).
2 (highest in liver transplants and lowest in kidney transplants).
3 ith quadrimembral amputations and a previous kidney transplant.
4 donor-derived KS in the recipient of a liver-kidney transplant.
5 ration decreasing the cost of pancreas after kidney transplant.
6 rate and odds of receiving a deceased donor kidney transplant.
7 t has a high propensity for recurrence after kidney transplant.
8 t, there are racial disparities in access to kidney transplant.
9 used by persistent hyperparathyroidism after kidney transplant.
10 y to CKD, which was followed by a preemptive kidney transplant.
11 ents who received their first deceased donor kidney transplants.
12 wn to trigger chronic allograft rejection in kidney transplants.
13 ual proportions of living donor, DBD and DCD kidney transplants.
14 differentiate rejection from other injury in kidney transplants.
15 8; P < 0.001) were associated with increased kidney transplants.
16 idates, and 1198 candidates (31.7%) received kidney transplants.
17 ld potentially improve graft survival in DCD kidney transplants.
18 ormed a total of 1553 adult first and second kidney transplants-1021 with a living donor, 532 with a
20 hundred sixty-five adults with PCKD received kidney transplants (303 tx alone, 161 simultaneous, 27 p
21 th children receiving a well HLA-matched DBD kidney transplant (83%, 95% CI, 80-86%, log rank test P
22 r children receiving a poorly HLA-matched LD kidney transplant (88%, 95% confidence interval [95% CI]
25 gdom, donation after circulatory death (DCD) kidney transplant activity has increased rapidly, but ma
28 recipient and the contralateral kidney to a kidney transplant alone (KTA) recipient (cohort from Feb
31 rolling hypercalcemia in these patients with kidney transplants and persistent hyperparathyroidism.
33 recipient is matched, or even in need of, a kidney transplant, and deceased donor initiated chains i
35 plement-dependent endothelial cell injury in kidney transplants, as assessed by expression of endothe
36 to treat study of 2587 candidates listed for kidney transplant at a single transplant center over 7 y
39 registry, patients who have received second kidney transplants between 1997 and 2009 were included.
40 an [SD] age, 49.6 [15.3] years) who received kidney transplants between 2004 and 2012, 488 (0.4%) had
41 neous pancreas and kidney and pancreas after kidney transplants between January 1994 and July 2013.
42 ing data, we identified first deceased donor kidney transplants between October 1, 1987, and December
44 ripts, and studied their expression in human kidney transplant biopsies with AMR and in an extended h
45 ion after donation after cardiac death (DCD) kidney transplants, but the impact of DGF on graft outco
47 haring data, we examined retrospectively all kidney transplant candidates (n = 369 103) and recipient
48 trospective cohort study in first-time adult kidney transplant candidates (N=161,308) using data from
49 odel to calculate likelihood of outcomes for kidney transplant candidates and demonstrate how this in
54 cross large areas of the United States, many kidney transplant candidates spend over 5 years waiting
56 a from 2003 to 2012 for adult deceased donor kidney transplant candidates was analyzed to evaluate pa
57 has limited efficacy for desensitization in kidney transplant candidates when up to 16 doses is give
58 f body surface area) in 10 highly sensitized kidney transplant candidates with alloantibodies against
59 es transplant eligibility by reducing BMI in kidney transplant candidates, but the effect of surgical
61 eater market competition was associated with kidney transplant center spatial clustering (P < 0.001).
68 oss was substantially higher (deceased donor kidney transplant [DDKT] without delayed graft function
69 an influence diagram that models generalized kidney transplant decisions and show how the influence d
71 e recently established that HIV-1 can infect kidney transplant epithelial cells in the absence of det
75 ies have facilitated compatible living-donor kidney transplants for end-stage renal disease patients
76 a from 13,789 patients who received a second kidney transplant from 1995 to 2011, of which 3868 had o
78 e-center evidence that patients who received kidney transplants from HLA-incompatible live donors had
79 the survival benefit for 1025 recipients of kidney transplants from HLA-incompatible live donors who
80 r-specific antibody: 89.2% for recipients of kidney transplants from incompatible live donors who had
81 ved longevity of HIV-positive individuals, a kidney transplant has become a viable option for many wh
84 lysis and Transplant Registry who received a kidney transplant in Australia between January 1, 2000,
85 pplied minimally invasive surgery to perform kidney transplant in individuals with body mass index (B
87 time trends in average eGFR at 1 year after kidney transplant in the United States in a cohort of 18
89 s of HLA-matched and mismatched living donor kidney transplants in 3 medical centers using hematopoie
90 f a mutant strain in high-risk recipients of kidney transplants, including 168 seronegative recipient
91 hibitors (CNI) nephrotoxicity to progressive kidney transplant injury remains debated, with little lo
94 decline in eGFR between years 1 and 3 after kidney transplant is common and strongly associated with
100 ysiologic reserve, is associated with longer kidney transplant (KT) length of stay (LOS), and modifie
102 national case-control study that included 51 kidney transplant (KT) recipients diagnosed with early (
103 Prevalence and clinical outcomes of MGUS in kidney transplant (KT) recipients have been previously r
106 al studies have described ED use rates among kidney transplant (KTx) recipients, and the factors asso
108 ith DGF: 10.815.221.4, P < 0.001; live donor kidney transplant [LDKT]: 18.136.774.2, P < 0.001) and m
109 ta2(neg) gammadelta T cells in recipients of kidney transplants may predict CMV infection resolution
113 ormation was obtained from Organ Procurement Kidney Transplant Network/United Network for Organ Shari
114 ording to quartiles of risk of mortality and kidney transplant on the basis of multivariable Cox mode
115 tibodies (DSAs) are associated with impaired kidney transplant outcome; however, whether these antibo
123 e and approved by the health authorities for kidney transplant patients is belatacept (Nulojix), a fu
124 , and screening for urologic malignancies in kidney transplant patients is warranted, and as such, th
126 hormone levels were comparable in adolescent kidney transplant patients receiving low-exposure mTOR i
131 the US Renal Data System, we identified 3245 kidney transplant patients who underwent PCI between Apr
132 crovesicle concentration in the plasma of 95 kidney transplant patients with allograft dysfunction an
133 ults demonstrate a complex urinary virome in kidney transplant patients with multiple viruses with se
134 explored in a cross-sectional analysis in 59 kidney transplant patients with SCC on CNI (KT-CNI-SCC)
136 this study, we evaluate whether in tolerant kidney transplant patients, the increased IL-10 producti
147 utcomes, for which the proportion of DCD:DBD kidney transplants performed is lower (25%; p < 0.0001),
150 reappearance of anti-PLA2R antibodies after kidney transplant predicts development of recurrent dise
153 rt (CYP3A5, ABCB1, and PXR) were analyzed in kidney transplant recipients (1995-2005, Leiden cohort,
154 we identified all adult (>/=18 years) first kidney transplant recipients (1996-2011) with ESRD attri
155 here were 13 trials (n = 9850) that included kidney transplant recipients (6 trials), patients who ha
156 sured by flow cytometry in 76 deceased donor kidney transplant recipients (DGF, n = 18; SGF, n = 34;
157 l acute kidney injury (AKI) occurred in four kidney transplant recipients (KDIGO grade 1: n = 3, grad
158 ittent hemodialysis treatment (CKD 5D) and 8 kidney transplant recipients (KT) with severe aortic val
159 opathy (PVAN) after BK virus reactivation in kidney transplant recipients (KTR) can compromise graft
160 associated with baseline viral serostatus in kidney transplant recipients (KTR) on sirolimus have not
163 s (CMV)-specific T cells in CMV-seronegative kidney transplant recipients (KTRs) have been attributed
165 escribe the results in a cohort of 10 stable kidney transplant recipients (median of 4.3 years posttr
166 TV load in the peripheral blood and AMR, 715 kidney transplant recipients (median, 6.3 years posttran
168 s in pediatric and adolescent deceased donor kidney transplant recipients aged 21 years or younger us
169 evalence proportions of 10%, 11%, and 18% in kidney transplant recipients and 10%, 9%, and 13% in liv
170 spective longitudinal study, we enrolled 168 kidney transplant recipients and 69 matched donors.
173 interventions on death and graft failure in kidney transplant recipients are not feasible, because t
175 ologies performed between 1998 and 2014 from kidney transplant recipients at the University of Maryla
176 tive observational study of 1996 adult first kidney transplant recipients between 1991 and 2010 in th
177 re (proximal humerus, forearm, hip) in adult kidney transplant recipients between 1994 and 2009, stra
178 r prospective cohort study of 83 nondiabetic kidney transplant recipients between 2008 and 2011.
179 ith an increased risk of graft loss in adult kidney transplant recipients but the association remains
180 y must be added to the current monitoring of kidney transplant recipients due to its relationship wit
181 sion analyses were performed on adult, first kidney transplant recipients during 1991 to 2010 (n = 14
182 lyomavirus (BKPyV) frequently reactivates in kidney transplant recipients during immunosuppressive th
183 al and transplant history from 977 prevalent kidney transplant recipients enrolled in the Malnutritio
186 e relevance of these cells in 100 unselected kidney transplant recipients followed prospectively for
187 udy 56 076 adult Medicare-primary first-time kidney transplant recipients from December 1999 to Octob
188 etrospective cohort study of 948 nondiabetic kidney transplant recipients from January 1, 2000, to De
191 enal Data System records of Medicare-insured kidney transplant recipients in 2000 to 2011 to determin
193 tment of IL-2RAb in pediatric and adolescent kidney transplant recipients is associated with at least
194 lthough current immunosuppressive therapy in kidney transplant recipients is effective, dosing is con
195 chronic hepatitis C virus (HCV) infection in kidney transplant recipients is limited because of the r
196 chronic hepatitis C virus (HCV) infection in kidney transplant recipients is limited because of the r
198 educing the risk of acute rejection in adult kidney transplant recipients is well established, a simi
202 er prospective randomized study in which 288 kidney transplant recipients receiving tacrolimus and pr
204 undertaken using single-antigen beads in 131 kidney transplant recipients returning to the transplant
205 his clinical trial, we randomized 90 de novo kidney transplant recipients shortly after transplantati
207 y were to describe the evolution of HRQOL in kidney transplant recipients to search for subgroups wit
208 records, and Medicare claims data for 16 308 kidney transplant recipients transplanted 2006 to 2008,
209 opensity score matched cohort study of adult kidney transplant recipients transplanted between May 1,
210 timal use, we describe the largest series of kidney transplant recipients treated with prophylactic e
213 denosumab to prevent bone loss in first-year kidney transplant recipients was associated with more fr
216 -two heart, 34 liver, 79 kidney, and 5 liver-kidney transplant recipients who completed treatment for
217 tched cohort study of 52 of 1476 consecutive kidney transplant recipients who developed postoperative
218 lected crossmatch positive living donor HLAi kidney transplant recipients who received their transpla
221 registry was reviewed for adult living donor kidney transplant recipients with BMI of 40 kg/m or grea
223 avirin-free regimen ledipasvir-sofosbuvir in kidney transplant recipients with chronic genotype 1 or
224 Patients: Treatment-naive or -experienced kidney transplant recipients with chronic genotype 1 or
225 avirin-free regimen ledipasvir-sofosbuvir in kidney transplant recipients with chronic genotype 1 or
231 d to have an acceptable safety profile among kidney transplant recipients with HCV genotype 1 or 4 in
232 d to have an acceptable safety profile among kidney transplant recipients with HCV genotype 1 or 4 in
233 human immunodeficiency virus/HCV coinfected kidney transplant recipients with ledipasvir-sofosbuvir
234 A group) with (i) 104 matched HLA-sensitized kidney transplant recipients with No DSA at D0 (No DSA g
236 with No DSA at D0 (No DSA group) and (ii) 47 kidney transplant recipients with preformed A, -B, -DR,
237 findings in the current study indicate that kidney transplant recipients with PV replication and smo
242 eded to identify the optimal DAA regimen for kidney transplant recipients, accounting for efficacy, t
243 R-146a in both allografts and urine of human kidney transplant recipients, and unilateral IRI in mice
244 e general population and in HCV-monoinfected kidney transplant recipients, but there are no data to g
246 de novo donor-specific antibodies (dnDSA) in kidney transplant recipients, especially in those with s
248 al to become clinically useful surrogates in kidney transplant recipients, including functional T cel
251 lyomavirus (BKV) in urinary tract cancers in kidney transplant recipients, suggesting that BKV could
252 rvational study involving 319 deceased-donor kidney transplant recipients, we assessed variations in
253 risk of acute rejection and graft loss in AA kidney transplant recipients, whereas neither baseline n
274 n, particularly within African American (AA) kidney transplant recipients; little is known about intr
277 on increased referral and improved equity in kidney transplant referral for patients on dialysis in G
278 al (the Bortezomib in Late Antibody-Mediated Kidney Transplant Rejection [BORTEJECT] Trial), we inves
280 d to those on maintenance dialysis or with a kidney transplant, RRs attenuated substantially, but ADP
282 a South Africa study involving 27 HIV-to-HIV kidney transplants showed promise, with 3- and 5-year pa
283 abase records for 9916 simultaneous pancreas-kidney transplants (SPKT) performed between 2000 and 201
284 d IRDs later received non-IRD deceased donor kidney transplants; the median KDPI of these non-IRD kid
286 rge cohort of children and young adults with kidney transplant to estimate the prevalence of abnormal
288 ent of donors was undertaken in a specialist kidney transplant unit in Pakistan to identify risk and
292 f death and higher likelihood of receiving a kidney transplant, we performed a cohort study of 469,57
294 al failure, especially at the early phase of kidney transplant when ischemia-reperfusion injury and c
295 e cohort analysis of pairs of deceased donor kidney transplants where 1 kidney was allocated to a sim
296 ctive treatment for most is a combined liver-kidney transplant, which requires life-long immune suppr
297 PrEdiction (ESCAPE) Study in 75 consecutive kidney transplants who received 6-month protocol biopsie
298 e patient who presented for a deceased donor kidney transplant with incidental finding of complete in
299 ared survival of patients opting for an HLAi kidney transplant with that of similarly sensitised pati
300 Over 100 000 patients are waiting for a kidney transplant, yet 3159 kidneys were discarded in 20
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