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1 essed, human immunodeficiency virus-negative renal transplant patient.
2 s and hemophagocytic syndrome in an asplenic renal transplant patient.
3 ng adult care is a vulnerable period for the renal transplant patient.
4 reviously unknown poxvirus rash illness in a renal transplant patient.
5 igen (HLA) antibodies (dnDSA) in the primary renal transplant patient.
6 ey allograft survival affecting up to 15% of renal transplant patients.
7 disease in immunosuppressed bone marrow and renal transplant patients.
8 spective study was undertaken in MMF-treated renal transplant patients.
9 alysis was used to estimate lymphoma risk in renal transplant patients.
10 ne and steroids as a maintenance regimen for renal transplant patients.
11 es and CNI toxicity after the first month in renal transplant patients.
12 L10 for detecting alloimmune inflammation in renal transplant patients.
13 , to cynomolgus monkeys and most recently to renal transplant patients.
14 netics of multiple doses of FTY720 in stable renal transplant patients.
15 for following the course of the infection in renal transplant patients.
16 iovascular risk attributable to BP burden in renal transplant patients.
17 he prevention of acute rejection episodes in renal transplant patients.
18 tilymphocyte antibody-resistant rejection in renal transplant patients.
19 ute to posttransplant bone loss in long-term renal transplant patients.
20 cause of renal allograft failure among adult renal transplant patients.
21 e in preventing acute rejection in cadaveric renal transplant patients.
22 uggest its use in the clinical management of renal transplant patients.
23 available than cyclosporine (CsA) in de novo renal transplant patients.
24 as a routine HLA antibody screening test for renal transplant patients.
25 t hypertension in cyclosporine (CsA)-treated renal transplant patients.
26 levels within the therapeutic range of human renal transplant patients.
27 osporine, in the postoperative management of renal transplant patients.
28 n cyclosporine A (CsA) bioavailability in 10 renal transplant patients.
29 stimating measured GFR (mGFR) changes in 110 renal transplant patients.
30 would guide immunosuppression management in renal transplant patients.
31 , and kidney biopsies were collected from 48 renal transplant patients.
32 d GC-MS-based metabolomic study on urines of renal transplant patients.
33 y of monitoring immunosuppressive therapy in renal transplant patients.
34 oming the standard of care for KS arising in renal transplant patients.
35 ion profile, a finding that was confirmed in renal transplant patients.
36 ociodemographic and clinical risk factors in renal transplant patients.
37 e vulgares and molluscum lesions in all four renal transplant patients.
38 reference tacrolimus (Prograf(R)) in stable renal transplant patients.
39 increased TNF-alpha when compared to stable renal transplant patients.
40 implications for the clinical management of renal transplant patients.
41 f the NFATc4 gene were genotyped in Hispanic renal transplant patients.
42 hr urine albumin excretion (n=189) in stable renal transplant patients.
43 ated with only two cases of disease, both in renal transplant patients.
44 dence and risk factors of NODAT in pediatric renal transplant patients.
45 irolimus (SRL) can improve graft function in renal transplant patients.
46 therapy is safe in immunologically high-risk renal transplant patients.
47 ons of new-onset diabetes mellitus (NODM) in renal transplant patients.
48 Hyperlipidemia affects the majority of renal transplant patients.
49 s or Neoral as primary immunosuppressant for renal-transplant patients.
51 se in control subjects (-19.8+/-3.0 bpm) and renal transplant patients (-23.9+/-4.9 bpm) (P<.001 vers
52 Viral DNA was present in the blood of some renal transplant patients (3/33 PCR-positive) but in non
53 titutions have reported favorable results in renal transplant patients after conversion from cyclospo
54 cyte antigen (HLA)-specific B lymphocytes in renal transplant patients after treatment with B-lymphoc
57 of human herpesvirus 8 (HHV-8) activation in renal transplant patients, an immunocompromised populati
58 Microscopic examination of stool from one renal transplant patient and of tracheal and gastric asp
59 idomic analysis of 70 unique samples from 50 renal transplant patients and 20 controls (n = 20), iden
60 ctive observational and database analysis of renal transplant patients and a physician questionnaire
61 ications of nonspecific immunosuppression in renal transplant patients and accounts for significant m
62 cytomegalovirus (CMV) disease in a group of renal transplant patients and assessed the role of viral
64 auses polyomavirus-associated nephropathy in renal transplant patients and hemorrhagic cystitis in bo
65 tion is associated with inferior survival in renal transplant patients, and ganciclovir (GCV) prophyl
67 ty-four urine samples were collected from 32 renal transplant patients at various stages posttranspla
68 d educators need to take explicit account of renal transplant patients' attitudes when evaluating ris
69 formulation is similar to Prograf in stable renal transplant patients, but data in de novo patients
70 idence of ischemic heart disease (IHD) among renal transplant patients can be attributed to the same
71 xpression data in 558 blood samples from 436 renal transplant patients collected across eight transpl
72 on does not offer a better GFR prediction in renal transplant patients compared with the MDRD Study e
74 dialysis patients is exceeded by that among renal transplant patients during the first 1 to 3 years
75 chocardiography) assessment were done in 165 renal transplant patients during the first year and afte
76 converting from Tac BID to Tac QD in stable renal transplant patients, especially in patients with t
77 open-label, parallel-group, 6-month study in renal transplant patients, FK778 (an investigational imm
80 changes after converting stable, maintenance renal transplant patients from CsA (once daily and twice
82 retrospective study of the first 75 primary renal transplant patients given alemtuzumab induction at
84 ion, whereas conventionally immunosuppressed renal transplant patients homozygous for a nonfunctional
87 mocystis isolates from 3 outbreaks of PCP in renal transplant patients in Germany, Switzerland, and J
88 Furthermore, analysis of data from 46,691 renal transplant patients in the United Network for Orga
91 l 20, 2004 and December 26, 2007 we enrolled renal transplant patients into a prospective, randomized
93 reactivation in immunosuppressed patients or renal transplant patients is the primary cause of polyom
94 tation, it is not known whether their use in renal transplant patients leads to excessive suppression
95 or precise in reflecting real GFR decline in renal transplant patients, making them unreliable for cl
96 common disease in most transplant patients, renal transplant patients more commonly experience urina
99 reteral ulceration with ureteral stenosis in renal transplant patients or hemorrhagic cystitis in bon
103 s that need special attention in the care of renal transplant patients, particularly modifiable facto
107 atory, randomized, 6-month study, 92 de novo renal transplant patients received everolimus, steroids,
108 -center, retrospective analysis of pediatric renal transplant patients receiving 24 weeks valganciclo
110 of predicted alloimmune quiescence in stable renal transplant patients receiving long-term immunosupp
113 chronic rejection by analyzing data from 245 renal transplant patients receiving Tacrolimus-based imm
114 suggest that steroid withdrawal in pediatric renal transplant patients receiving tacrolimus-based imm
115 group (P < 0.001) compared with nondiabetic renal transplant patients receiving the same immunosuppr
116 al of steroid withdrawal was conducted among renal transplant patients receiving triple immunosuppres
117 survival for both cadaveric and living-donor renal-transplant patients receiving either Neoral or tac
118 trospective cohort study of Medicare primary renal transplant patients reported in the United States
123 monitoring (ABPM) for risk stratification in renal transplant patients still remains poorly defined.
125 We present a case of CMV vasculitis in a renal transplant patient that caused middle and left col
129 We evaluated antibody binding of waitlisted renal transplant patients to 3 glycan knockout (KO) pig
130 actic ganciclovir (GCV) is used in high-risk renal transplant patients to prevent acute cytomegalovir
131 randomized, exploratory 6-month study of 92 renal transplant patients treated de novo with concentra
132 predisposing factors for dyslipidemia among renal transplant patients treated for up to 6 years with
134 t doses up to 5.0 mg/day for 28 days, stable renal transplant patients treated with FTY720 in combina
137 vivo kinetics of lymphocytes in CMV-infected renal transplant patients using longitudinal samples com
138 roach to regulatory T-cell (Treg) therapy in renal transplant patients, using a delayed infusion prot
139 unosuppression for immunologically high-risk renal transplant patients usually involves antithymocyte
146 Tacrolimus dose requirements of 206 stable renal transplant patients were related to MDR-1 genotype
151 rapamycin, we have occasionally encountered renal transplant patients who develop unexpected severe
155 and HLA-DQ antigens were determined for 703 renal transplant patients who had no detectable donor-sp
157 ose was to determine the compliance rates of renal transplant patients who received their immunosuppr
159 ment, by allograft autotransplantation, of a renal transplant patient with an invasive carcinoma of t
161 m was used to study 37 serum samples from 15 renal transplant patients with (n=10) and without (n=5)
162 In this single-center study, 26 living-donor renal transplant patients with a positive level of de no
163 is associated with higher serum IL-17A among renal transplant patients with acute rejection, linking
164 levels were significantly elevated in human renal transplant patients with acute VR (n = 16) compare
165 l study to compare serum LG3 levels in human renal transplant patients with acute VR, tubulo-intersti
168 inct condition which should be considered in renal transplant patients with ascites, after all other
169 y and safety of sofosbuvir and ledipasvir in renal transplant patients with chronic HCV infection.
170 s of maintenance immunosuppressive agents in renal transplant patients with chronic viral hepatitis.
171 determine changes in anti-HLA antibodies in renal transplant patients with COVID-19 and compare the
174 ipid profiles in stable cyclosporine-treated renal transplant patients with established hyperlipidemi
175 longitudinal, open-label trial, MMF-treated renal transplant patients with gastrointestinal symptoms
176 non-smokers were included (40 CsA-medicated renal transplant patients with GO [GO+; n = 20] or witho
177 tocellular carcinoma, and hepatic failure in renal transplant patients with HCV infection are scarce.
179 y, no guidelines exist for the management of renal transplant patients with impaired glucose toleranc
181 proposed as ways to prolong the survival of renal transplant patients with ischemic heart disease.
183 gree of unnoticed tacrolimus overexposure in renal transplant patients with mild diarrhea while on tr
184 flow reactivity with clinical outcome among renal transplant patients with negative preoperative cyt
185 iopsies of a well-characterized cohort of 28 renal transplant patients with no rejection (Ctrl), dela
186 that have the ability to distinguish between renal transplant patients with no rejection and those wi
188 determine if any aspects of the treatment of renal transplant patients with pancreatitis were of part
189 transcripts in biopsy samples from 42 stable renal transplant patients with posttransplant hypertensi
190 hat co-infection with BKV and SV40 occurs in renal transplant patients with PVN, suggesting that SV40
192 the largest single medical center series of renal transplant patients with SLE, recurrent LN was mor
193 om a prospective, observational cohort of 59 renal transplant patients with surveillance or indicatio
194 udy, we assessed the outcome of all (n = 95) renal transplanted patients with pretransplant cancer di
195 uperior immunosuppressive agent in pediatric renal transplant patients, with excellent short- and med
196 n activity, was measured in stable pediatric renal transplant patients, with healthy children used as