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1 event cytomegalovirus (CMV) infections after solid organ transplant.
2 s of primary cutaneous T-cell lymphoma after solid organ transplant.
3 the short- and long-term clinical outcome of solid organ transplant.
4 s) were saved to date during the 25 years of solid-organ transplant.
5 typically related to immunomodulation during solid-organ transplant.
6 plants and show great promise for women with solid-organ transplant.
7 he most common opportunistic infection after solid-organ transplant.
8 nd 2018 with a diagnosis of amyloidosis post solid-organ transplant.
9 gs) in both murine and human recipients of a solid-organ transplant.
10 the major obstacle for long-term survival of solid organ transplants.
11 nt recipients and may be applicable to other solid organ transplants.
12 plant are similar to those reported in other solid organ transplants.
13 antibodies in acute and chronic rejection of solid organ transplants.
14 ts with cancer or recipients of stem cell or solid organ transplants.
15 ansplantation of hematopoietic stem cells or solid organ transplants.
16 ffects on graft survival in several types of solid organ transplants.
17 h chronic hepatitis E who were recipients of solid-organ transplants.
18 tion is associated with the deterioration of solid-organ transplants.
19 ia among recipients of hematopoietic-cell or solid-organ transplants.
21 is the first description of amyloidosis post solid-organ transplant; 30 cases among 5112 amyloid pati
22 KP infections occurred more frequently among solid organ transplant (31%) and dialysis (17%) patients
23 he records of 59 patients who had received a solid-organ transplant (37 kidney-transplant recipients,
24 he registry linkages yielded data on 175,732 solid organ transplants (58.4% for kidney, 21.6% for liv
26 Four patients were immunosuppressed after solid organ transplant and all were receiving blood pres
27 plications for sensitized patients receiving solid organ transplants and antibody-mediated rejection
28 apy for ESBL-producing Enterobacteriaceae in solid organ transplants and MCS device recipients are es
29 d 123 from the literature), 63 had undergone solid-organ transplant and 39 had human immunodeficiency
34 the liver less prone to rejection than other solid organ transplants, and reaction to local injury, s
35 to induce rejection compared with most other solid organ transplants, and simultaneous transplantatio
36 g transplantation is among the lowest of all solid-organ transplants, and current diagnostic tests of
37 l infarction, stroke, hemorrhagic shock, and solid organ transplant are particularly prone to cause I
40 omen of reproductive age who have received a solid-organ transplant are at risk for unplanned pregnan
42 equirement for immunosuppression compared to solid organ transplants because of the inherent immune p
43 ded patients with end-stage renal disease or solid organ transplants because very few are uninsured.
46 w one of the most common bacterial causes of solid-organ transplant donor-derived infection reported
47 this retrospective analysis of UNOS data for solid-organ transplant during a 25-year period (Septembe
48 n 2 million life-years were saved to date by solid-organ transplants during a 25-year study period.
52 were seen in recipients receiving noncardiac solid organ transplants from simvastatin-treated donors.
53 ssessed graft survival through 1 year of all solid organs transplanted from 370 donors who had been r
54 d trial, recipients of hematopoietic-cell or solid-organ transplants (>=18 years of age, with CMV rea
55 measurements as infection risk markers after solid organ transplant has not been fully investigated.
58 partners, bridges research in the fields of solid organ transplant, hematopoietic cell transplant, a
59 lant failure or rejection (HR 3.2), previous solid organ transplant (HR 1.7), and several comorbiditi
60 ctious disease consultation in recipients of solid organ transplant is associated with increased LOS
62 on of continuous distribution models for all solid organ transplants may allow for minimization of th
63 thritis (n = 97), hematopoietic stem-cell or solid organ transplant (n = 26), or a general cohort of
65 e to ten-fold risk (25 to 30 fold risk after solid organ transplant) of colorectal cancer (CRC) than
67 sed by Nocardia thailandica in a 66-year-old solid organ transplant patient from Connecticut, which w
69 unoglobulin was identified in only 3% of all solid organ transplant patients pretransplant (n=34).
70 ill, oncologic or stem cell transplant, and solid organ transplant patients showed a relationship be
72 We studied six cases of CMV replication in solid organ transplant patients whose genotypic testing
74 (Carbapenem-Resistant Enterobacteriaceae in Solid Organ Transplant Patients) has provided pivotal da
80 ed all cryptosporidiosis cases identified in solid organ transplanted patients between 2006 and 2010
81 trated efficacy in preventing CMV disease in solid-organ transplant patients as well as congenital di
82 ional markers aimed at identifying long-term solid-organ transplant patients at high risk of developi
83 We assessed kidney function and histology in solid-organ transplant patients during HEV infection.
85 th significant morbidity and mortality among solid-organ transplant patients, but approaches to diagn
88 g transplantation lags behind that for other solid organ transplants, primarily because of allograft
89 ew will discuss key studies in the different solid organ transplants, recent reports of adverse event
91 even patients (10 with HIV infection and one solid-organ transplant recipient) developed tuberculosis
95 The increased incidence of skin cancers in solid organ transplant recipients (OTR) has been well es
96 reported an increased risk of skin cancer in solid organ transplant recipients (OTRs), no study has e
97 ntibody response to the 2009-H1N1 vaccine in solid organ transplant recipients (SOTR) and its clinica
98 s on the use of generic immunosuppression in solid organ transplant recipients (SOTR) based on a revi
106 view available data on coccidioidomycosis in solid organ transplant recipients and candidates seeking
107 iabetes mellitus (PTDM) affects up to 50% of solid organ transplant recipients and compromises long-t
108 e multiple risk factors for CNS processes in solid organ transplant recipients and establishes a time
110 excess risk are similar to those observed in solid organ transplant recipients and patients with auto
111 tion of pretransplantation HLA antibodies in solid organ transplant recipients and, in particular, th
116 -scale retrospective study that included 255 solid organ transplant recipients confirms that ribaviri
118 testing novel immunotherapy combinations in solid organ transplant recipients designed to uncouple a
119 n addition, a significant number of nonrenal solid organ transplant recipients develop chronic kidney
122 ssociated cluster of febrile illness among 3 solid organ transplant recipients from a common donor.
124 TICIPANTS: Cohort study using linked data on solid organ transplant recipients from the US Scientific
130 ntions to prevent nonmelanoma skin cancer in solid organ transplant recipients have not been summariz
131 ntified a Swedish population-based cohort of solid organ transplant recipients in the National Patien
132 ecipients, which contains information on all solid organ transplant recipients in the United States,
137 eatment outcomes during CMV infection in 291 solid organ transplant recipients receiving valganciclov
138 n-resistant Enterococcus faecium (LR-VRE) in solid organ transplant recipients remain uncommon, they
139 ng Enterobacteriaceae and CRE carriage among solid organ transplant recipients to inform management o
140 Treatment failure or relapse is common in solid organ transplant recipients treated for cytomegalo
141 cancer was assessed among 118,440 Caucasian solid organ transplant recipients using multivariate Cox
145 high-throughput gene expression datasets of solid organ transplant recipients were retrieved from th
149 andemic of SARS-CoV-2, there is concern that solid organ transplant recipients will be particularly v
151 ates that elevated osteoprotegerin levels in solid organ transplant recipients with CMV infection may
152 ms, clinical severity, and disease course in solid organ transplant recipients with COVID-19, includi
153 We herein report our initial experience with solid organ transplant recipients with SARS-CoV-2 infect
154 75] days before ICU admission), 4 (10%) were solid organ transplant recipients, and 10 (27%) were inf
155 view the current status of CMV resistance in solid organ transplant recipients, and provide diagnosti
156 ears to be safe and immunogenic in pediatric solid organ transplant recipients, but there are few dat
158 erebral vasculature that occurs in 0.5-5% of solid organ transplant recipients, most commonly associa
160 ctivation can cause significant morbidity in solid organ transplant recipients, particularly BK virus
161 hough diarrhea is a frequent complaint among solid organ transplant recipients, the contribution of i
162 tors for invasive mold infections among 1101 solid organ transplant recipients, thereby strengthening
164 er phase II trial, 152 treatment-naive adult solid organ transplant recipients, with CD20(+) PTLD unr
165 D) is an increasingly important diagnosis in solid organ transplant recipients, with rising incidence
198 and risk factors of obesity among pediatric solid-organ transplant recipients (heart, lung, liver, k
199 and risk factors of obesity among pediatric solid-organ transplant recipients (heart, lung, liver, k
200 umatoid arthritis (n = 199), 9.0 to 20.0% in solid-organ transplant recipients (n = 197), 0% to 5.8%
204 0 fresh CMV DNA-positive plasma samples from solid-organ transplant recipients (SOTRs) were tested.
205 ted to occur during transitions of care, and solid-organ transplant recipients are at an increased ri
207 ical trials with expanded T(regs) in T1D and solid-organ transplant recipients are limited by poor T(
209 ta of pandemic influenza A H1N1 infection in solid-organ transplant recipients have been described, b
212 the effects of ribavirin as monotherapy for solid-organ transplant recipients with prolonged HEV vir
213 inhibitors, patients receiving hemodialysis, solid-organ transplant recipients, and patients with can
214 fluence susceptibility to CMV replication in solid-organ transplant recipients, particularly in patie
215 onmelanoma skin cancer is well recognized in solid-organ transplant recipients, the risk of skin canc
216 CMV) disease remains an important problem in solid-organ transplant recipients, with the greatest ris
223 drug-resistant/recurrent cytomegalovirus in solid-organ transplant recipients.METHODSIn the present
227 iew is to discuss the current and historical solid organ transplant-related disruptions in the supply
230 economics willingness-to-pay threshold to a solid organ transplant setting by coining a new metric:
232 Data describing antibiotic allergies among solid organ transplant (SOT) and hematopoietic cell tran
233 cause of morbidity and mortality among both solid organ transplant (SOT) and hematopoietic stem cell
234 ous diseases physicians in persons receiving solid organ transplant (SOT) between May 2008 and Decemb
236 for exercise training in adult and children solid organ transplant (SOT) candidates and recipients a
238 cal and molecular pretransplant screening in solid organ transplant (SOT) donors and recipients in no
240 s a potentially fatal disorder arising after solid organ transplant (SOT) or hematopoietic stem cell
246 Hematopoietic cell transplant (HCT) and solid organ transplant (SOT) recipients are at increased
250 tis jirovecii pneumonia (PJP) prophylaxis in solid organ transplant (SOT) recipients at increased ris
251 ause severe infections in seronegative adult solid organ transplant (SOT) recipients but can be preve
254 ecific cytotoxic T lymphocytes (EBV-CTLs) to solid organ transplant (SOT) recipients has been shown s
256 , and immune responses in HIV-infected adult solid organ transplant (SOT) recipients on antiretrovira
257 ological response (SVR) in a large cohort of solid organ transplant (SOT) recipients with chronic HEV
258 e of immune reconstitution syndrome (IRS) in solid organ transplant (SOT) recipients with cryptococco
259 We sought to determine whether a subset of solid organ transplant (SOT) recipients with high likeli
260 ical characteristics, risks, and outcomes in solid organ transplant (SOT) recipients with zygomycosis
261 enteritis can cause intractable diarrhea in solid organ transplant (SOT) recipients, for which there
262 D-19 among immunosuppressed patients such as solid organ transplant (SOT) recipients, who are at pres
272 utcomes associated with histoplasmosis after solid organ transplant (SOT), we report a large series o
273 med a multicenter, International analysis of solid organ transplant (SOT)-related primary central ner
279 ad immunosuppression (120; 82.8%), including solid organ transplant (SOT; 33.8%), autoimmunity (15.9%
281 Patients waitlisted for and recipients of solid organ transplants (SOT) are perceived to have a hi
282 gained over the years shows that, similar to solid organ transplants (SOT), human VCA can also develo
287 econstitution inflammatory syndrome (IRS) in solid-organ transplant (SOT) recipients are not known.
288 ding bacteremia caused by these organisms in solid-organ transplant (SOT) recipients is lacking.
293 jection, which is in sharp contrast to other solid organ transplants, such as kidney, lung, and heart
294 ng a significant clinical problem across all solid organ transplants, there are limited therapeutics
295 inking hematopoietic chimerism induction and solid organ transplant tolerance, the mechanistic requir
296 how preexisting autoreactive T cells affect solid-organ transplants under these conditions is unknow
297 ividuals with inflammatory bowel diseases or solid-organ transplants, virome dynamics in allogeneic h
299 ransplants and reduced long-term survival of solid organ transplants, we hypothesized that convention