コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ged >=50 years (19 transplant candidates, 20 transplant recipients).
2 t live birth rate (defined as live birth per transplanted recipient).
3 istant Cytomegalovirus retinitis in a kidney transplant recipient.
4 nt, 1 heart transplant recipient, and 1 lung transplant recipient.
5 ded: infant ALL, relapsed ALL, and stem cell transplant recipients.
6 cted DDD was rare, occurring in 0.18% of all transplant recipients.
7 n uncommon opportunistic infection in kidney transplant recipients.
8 ence to immunosuppression in pediatric liver transplant recipients.
9 ression in the growing population of elderly transplant recipients.
10 urologic surgeries, and nonrenal solid-organ transplant recipients.
11 re illness and a high mortality rate in lung transplant recipients.
12 ns to support self-management in solid organ transplant recipients.
13 mmune-mediated kidney diseases and to kidney transplant recipients.
14 ials of eHealth interventions in solid organ transplant recipients.
15 prognosis of female compared with male heart transplant recipients.
16 re collected from the Scientific Registry of Transplant Recipients.
17 h moderate to severe AKI in pediatric kidney transplant recipients.
18 o fatal hyperammonemia syndrome (HS) in lung transplant recipients.
19 tify risk factors for stroke death in kidney transplant recipients.
20 ay 31, 2017 using the Scientific Registry of Transplant Recipients.
21 ders, patients with liver disease, and liver transplant recipients.
22 ics were gleaned from Scientific Registry of Transplant Recipients.
23 pulations, it has not been assessed in heart transplant recipients.
24 tory cells isolated from sex-mismatched lung transplant recipients.
25 edominated (51%) in kidney, liver, and heart transplant recipients.
26 prophylaxis for CMV prevention in D+R- liver transplant recipients.
27 re examined using the Scientific Registry of Transplant Recipients.
28 s with postreperfusion damage in human liver transplant recipients.
29 cells and B cells during ABMR in 105 kidney transplant recipients.
30 the potential to severely impact solid organ transplant recipients.
31 d organ donors, deceased donor families, and transplant recipients.
32 bruary 2017 using the Scientific Registry of Transplant Recipients.
33 vailed as digestive tract pathogens in liver transplant recipients.
34 arable to those previously reported in renal transplant recipients.
35 isk scores on a contemporary cohort of heart transplant recipients.
36 ll as reduction of CNIs for pediatric kidney transplant recipients.
37 es of secondary stroke prevention for kidney transplant recipients.
38 ong heart, lung, liver, pancreas, and kidney transplant recipients.
39 ere identified in the Scientific Registry of Transplant Recipients.
40 ic approach has never been reported in liver transplant recipients.
41 ant outcomes is highly variable among kidney transplant recipients.
42 ultimately improved the outcomes of infected transplant recipients.
43 are limited data describing COVID-19 in lung transplant recipients.
44 ed pathways that overlapped with diabetes in transplant recipients.
45 fever has never previously been reported in transplant recipients.
46 RS-CoV-2 and how it affects organ donors and transplant recipients.
47 ading cause of mortality in kidney and liver transplant recipients.
48 tation, rarely occurs in kidney and pancreas transplant recipients.
49 e involved in regulating lung injury in lung transplant recipients.
50 d outcomes of COVID-19 infection among organ transplant recipients.
51 y in solid organ and hematopoietic stem cell transplant recipients.
52 new opportunities to improve the outcomes of transplant recipients.
53 s retrospective study included 282 HCC liver transplant recipients.
54 unosuppression in a clinical trial of kidney transplant recipients.
55 as evaluated in 2055 biopsies from 775 renal transplant recipients.
56 r prophylaxis for 100 days in 205 D+R- liver transplant recipients.
57 tment of tacrolimus-induced hyperglycemia in transplant recipients.
58 s, and as digestive tract pathogens in liver transplant recipients.
59 costs compared to prophylaxis in D+R- liver transplant recipients.
60 n in immunosuppressed patients, specifically transplant recipients.
61 nts, and Pseudomonas aeruginosa (9%) in lung transplant recipients.
62 nancy that limit the health and longevity of transplant recipients.
63 antly associated with DGF in pediatric renal transplant recipients.
64 factor of urothelial carcinoma (UC) in renal transplant recipients.
65 ith allograft dysfunction in pediatric liver transplant recipients.
66 es of 7 renal transplant recipients, 1 liver transplant recipient, 1 heart transplant recipient, and
67 reatment modalities, and outcomes of 7 renal transplant recipients, 1 liver transplant recipient, 1 h
70 ng clinically and biochemically stable liver transplant recipients, a subset with histological and tr
71 R antibodies in 2 cohorts of pediatric liver transplant recipients: a stable control cohort with norm
73 ndings indicate that immunosuppressed kidney transplant recipients admitted to the hospital with acut
76 : NRP and HOPE in cDCD achieved similar post-transplant recipient and graft survival rates exceeding
77 cember 2018) comprising 4 transgender kidney transplant recipients and 2 transgender living donors wa
78 neumonia has dramatic consequences in kidney transplant recipients and a targeted prophylaxis based o
79 ccurred as urinary tract pathogens in kidney transplant recipients and as digestive tract pathogens i
81 of acute and cGVHD in pancreas after kidney transplant recipients and be able to recognize the clini
82 itus (PTDM) affects up to 50% of solid organ transplant recipients and compromises long-term outcomes
83 r retrospective cohort study of primary lung transplant recipients and examined risk factors for DSA
84 olitis [LB]) distribution, is common in lung transplant recipients and increases the risk for chronic
87 pairment in mice with dietary obesity and in transplant recipients and restored immunoquiescence in h
88 e how allergy testing should be performed in transplant recipients and to better understand the impac
89 ients, 1 liver transplant recipient, 1 heart transplant recipient, and 1 lung transplant recipient.
90 urinary pathogens in heart, lung, and kidney transplant recipients, and as digestive tract pathogens
91 s achievable and safe in living-donor kidney transplant recipients, and is associated with fewer infe
92 deficits in long-term potentiation (LTP) in transplant recipients, and LTP impairment in TRANSWT mic
93 ts and as digestive tract pathogens in liver transplant recipients, and Pseudomonas aeruginosa (9%) i
95 been shown to protect seronegative women and transplant recipients, and we should know soon whether t
96 PA(+/0) mice) and of SR-uPA(+/0) bone marrow transplant recipients, and we used bioinformatic tools t
101 with expanded T(regs) in T1D and solid-organ transplant recipients are limited by poor T(reg) engraft
105 ll summarize the physiology of acute pain in transplant recipients, assess the impact of opioid use o
106 ays during IRI, we treated syngeneic cardiac transplant recipients at 1-hour posttransplant with Anak
107 We identified hospitalized adult kidney transplant recipients at 12 transplant centers in the Un
108 A similar pattern was observed in heart transplant recipients at both elevated and standard risk
111 ttransplant among 445 consecutive intestinal transplant recipients at our institution since 1994.
113 egistry data from the Scientific Registry of Transplant Recipients between 2006 and 2017, we compared
115 hods: We enrolled 156 of the 209 double lung transplant recipients between December 2017 and March 20
118 l blood samples obtained from 67 human liver transplant recipients both pre- [portal vein (PV) sample
119 It is widely used in hematopoietic cell transplant recipients but is infrequently utilized after
120 tancy and refusal in the general population, transplant recipients can no longer rely on herd immunit
121 verage of immunosuppressant drugs for kidney transplant recipients ceases 36 months after transplanta
123 spective study that included 255 solid organ transplant recipients confirms that ribavirin is highly
126 Renal Data System and Scientific Registry of Transplant Recipient data to compare waitlist- and popul
134 d mortality using the Scientific Registry of Transplant Recipients database for all kidney transplant
137 ed mean difference in overall EF skills with transplant recipients demonstrating worse EF (g = 0.40;
138 el immunotherapy combinations in solid organ transplant recipients designed to uncouple antitumor and
139 ients to determine how many pediatric kidney transplant recipients developed delayed graft function (
142 ot be used in high-immunological risk kidney transplant recipients due to a perceived increased risk
143 ontroversy about the use of immunotherapy in transplant recipients due to the risk of rejection.
144 for the development of de novo DSA in kidney transplant recipients during the first-year posttranspla
146 tudy conducted a serial study of human heart transplant recipients evaluating cardiac effects of diab
147 In the largest national series of EVLP lung transplant recipients, EVLP is associated with early rec
149 effective in treating CMV-infections in lung transplant recipients failing on currently available ant
150 ere obtained from the Scientific Registry of Transplant Recipients for adults listed and removed from
151 ticenter Deceased Donor Study of 2430 kidney transplant recipients from 1298 donors, we assessed the
153 atabase was reviewed to identify adult liver transplant recipients from 2002 through 2016 with MELD s
154 g data, HCV-infected adult first-time kidney transplant recipients from 2014 to 2017 were examined.
155 TR) to study 141 661 Medicare-primary kidney transplant recipients from January 1, 1999 to December 3
157 ted 296 807 adult (age > 17) solitary kidney transplant recipients from the Scientific Registry of Tr
159 ipient survival (as reported for other organ transplant recipients), graft survival, and uterus trans
160 dosis (group 1) and propensity score-matched transplant recipients (group 2, n = 81) with nonamyloido
162 d treatment of CMV infections and disease in transplant recipients has been further improved with the
163 f viruses that cause important infections in transplant recipients has been the standard of care for
166 ctors of obesity among pediatric solid-organ transplant recipients (heart, lung, liver, kidney, multi
167 an be safely withdrawn in a subset of kidney transplant recipients, immune mechanisms that underlie s
168 st reported case of yellow fever in a kidney transplant recipient in Brazil and the re-emergence of a
170 and recipient CMV-seronegative (D+R-) liver transplant recipients in the current era are incompletel
171 IV-positive to HIV-positive kidney and liver transplant recipients in the USA were examined for evide
172 or allo-sensitization in previously tolerant transplant recipients in whom tolerance maintenance is d
173 report four cases of COVID-19 in solid organ transplant recipients including recipients of kidney, li
176 lmonary disease or interstitial lung disease transplant recipients is associated with alterations in
178 Currently, 1 in 6 pediatric solid organ transplant recipients is hospitalized with a vaccine-pre
179 ving this, we studied Scientific Registry of Transplant Recipients kidney offer data for 3642 pediatr
181 n therapy is frequently prescribed to kidney transplant recipients (KTRs) for prevention and treatmen
183 n D (1,25D) predict renal outcomes in kidney transplant recipients (KTRs), with conflicting results.
186 munosuppression Medicare coverage for kidney transplant recipients led to lower costs of -$3077 and 0
187 tory syncytial virus (RSV) infection in lung transplant recipients (LTRs) causes mortality rates of 1
197 etween 2006 and 2017, we compared 2048 liver transplant recipients of steatotic livers with 69 394 re
199 disease treatment in hematopoietic stem cell transplant recipients often results in prolonged or inde
200 he clinical course and management of a liver transplant recipient on hemodialysis, who presented with
205 study in pediatric (>=1 to <18 years) kidney transplant recipients randomized at 4 to 6 weeks posttra
206 the randomized SCHEDULE trial, de novo heart transplant recipients received (1) everolimus with reduc
207 ysis suggests that in hypersensitized kidney transplant recipients receiving tacrolimus-based immunos
209 (+) T cells-in blood samples from 284 kidney transplant recipients recruited 1 year post-transplant a
210 sure immune function in the immunosuppressed transplant recipient relative to infectious risk and all
214 ommunication shares a protocol for donor and transplant recipient selection during the coronavirus di
215 linical picture is seen, teams managing lung transplant recipients should be aware of this potential
218 s, we used 2010-2018 Scientific Registry for Transplant Recipients (SRTR) data to identify 92 081 adu
219 e actual DDs from the Scientific Registry of Transplant Recipients (SRTR) data, simulations extend ov
220 S) data linked to the Scientific Registry of Transplant Recipients (SRTR) to study 141 661 Medicare-p
224 and confidence in managing HCV infection in transplant recipients that in turn has impacted the soli
227 a regarding the risk of cancer recurrence in transplant recipients, the goal of the AST-sponsored con
233 omes, and chemokine and cytokine response in transplant recipients to immunocompetent, nontransplant
234 9 study in which we randomized stable kidney transplant recipients to Tac withdrawal or maintenance o
235 single-center cohort of 64 orthotopic heart transplant recipients transplanted between 1994 and 2014
236 study was conducted across all single kidney transplant recipients, transplanted between 2011 and 201
237 In view of the recent literature, kidney transplant recipients treated by belatacept immunosuppre
238 e compared with a cohort of Medicare-insured transplant recipients, using multivariable survival anal
239 fer of circulating sEVs harvested from human transplant recipients varies depending on the type of tr
240 The impact of these therapies in solid organ transplant recipients was not assessed in clinical trial
242 Data System, and the Scientific Registry of Transplant Recipients, we compared population-level char
243 ighly phenotyped prospective cohort of heart transplant recipients, we identified 4 CAV trajectories
246 In an observational pilot study, 28 lung transplant recipients were enrolled in a novel postdisch
247 itive to HIV-positive kidney and eight liver transplant recipients were followed from March, 2016, to
248 IV-positive to HIV-positive kidney and liver transplant recipients were followed in three hospitals i
253 hput gene expression datasets of solid organ transplant recipients were retrieved from the Gene Expre
254 iorgan recipients compared with single-organ transplant recipients, which raise ethical questions reg
255 rt, we presented a 63-year-old female kidney transplant recipient who presented with dyspnea and coug
256 port, we present a dual-organ (heart/kidney) transplant recipient who was found to have COVID-19 and,
258 HR: (1.84) 1.91(1.98) , P < .001) for kidney transplant recipients who developed an infection, althou
260 estimated from a cohort of privately insured transplant recipients who receive lifelong immunosuppres
261 r retrospective study of stem cell and organ transplant recipients who received letermovir for the tr
262 proximately 33.6% of nondiabetic solid organ transplant recipients who received tacrolimus developed
263 is retrospective study included 28 pediatric transplant recipients who underwent a total of 32 (18)F-
265 ARS-CoV-2, there is concern that solid organ transplant recipients will be particularly vulnerable to
266 sessed cost-effectiveness between cohorts of transplant recipients willing and unwilling to receive H
267 e reporting the first case of CG in a kidney transplant recipient with kidney disease of unknown caus
268 -PD-1) for ~9 months to a 57-year-old kidney transplant recipient with metastatic cutaneous squamous
273 ong with serum antibody testing in 18 kidney transplant recipients with active coronavirus disease 20
274 in immunosuppressive therapy for all kidney transplant recipients with active COVID-19 may not be re
280 ion of the effects of immunomodulators among transplant recipients with COVID-19 infection will be im
281 severity, and disease course in solid organ transplant recipients with COVID-19, including two hospi
283 There are limited data on the outcome of transplant recipients with familial Mediterranean fever
284 Retrospective cohort study evaluating renal transplant recipients with first AMR episodes treated wi
286 e conducted a retrospective review of kidney transplant recipients with metastatic cancer who receive
288 lantation (CLKT) improves survival for liver transplant recipients with renal dysfunction; however, t
289 port our initial experience with solid organ transplant recipients with SARS-CoV-2 infection at two c
290 ood mononuclear cells were collected from 30 transplant recipients with self-limiting EBV DNAemia (SL
291 al prophylaxis in 205 CMV-seronegative liver transplant recipients with seropositive donors aged olde
292 hylaxis for high-risk CMV-seronegative liver transplant recipients with seropositive donors, high rat
294 olled trial involving 130 nondiabetic kidney transplant recipients with stable function between 3 and
296 aimed to compare the stroke deaths in kidney transplant recipients with the general population and id
297 recommend for or against screening of renal transplant recipients within 1 month, patients with high
298 ces rates of acute rejection in adult kidney transplant recipients, yet little is known about its eff
299 Comorbidity is increasingly common in kidney transplant recipients, yet the implications for transpla
300 ounty-level County Health Ranking data using transplant recipient zip code, and nationwide County Hea