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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 cularized cornea behaves like a vascularized solid organ transplant.
5 proved survival for patients with GVHD after solid organ transplant.
6 ective in reducing the incidence of GVD in a solid organ transplant.
7 typically related to immunomodulation during solid-organ transplant.
8 plants and show great promise for women with solid-organ transplant.
9 he most common opportunistic infection after solid-organ transplant.
10 s) were saved to date during the 25 years of solid-organ transplant.
11 the major obstacle for long-term survival of solid organ transplants.
12 nt recipients and may be applicable to other solid organ transplants.
13 plant are similar to those reported in other solid organ transplants.
14 antibodies in acute and chronic rejection of solid organ transplants.
15 on associated with chronic rejection (CR) of solid organ transplants.
16 of NKG2D and its ligands in the rejection of solid organ transplants.
17 BS has rarely been reported in recipients of solid organ transplants.
18 h chronic hepatitis E who were recipients of solid-organ transplants.
19 tion is associated with the deterioration of solid-organ transplants.
20 les for NK cells in reactivity to tissue and solid-organ transplants.
21 ion developed in two groups of recipients of solid-organ transplants.
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 f EBV-associated B-cell lymphomas is seen in solid organ transplant and bone marrow transplant recipi
28 tting, we report five new cases of GBS after solid organ transplant and summarize five other cases pr
29 apy for ESBL-producing Enterobacteriaceae in solid organ transplants and MCS device recipients are es
30 d 123 from the literature), 63 had undergone solid-organ transplant and 39 had human immunodeficiency
32 or neurologic illness, autoimmune disorders, solid organ transplant, and other significant comorbid c
34 to induce rejection compared with most other solid organ transplants, and simultaneous transplantatio
35 g transplantation is among the lowest of all solid-organ transplants, and current diagnostic tests of
39 omen of reproductive age who have received a solid-organ transplant are at risk for unplanned pregnan
41 ded patients with end-stage renal disease or solid organ transplants because very few are uninsured.
42 rejection (SCR) is a known entity in various solid organ transplants but not in intestinal transplant
45 w one of the most common bacterial causes of solid-organ transplant donor-derived infection reported
46 this retrospective analysis of UNOS data for solid-organ transplant during a 25-year period (Septembe
47 n 2 million life-years were saved to date by solid-organ transplants during a 25-year study period.
51 n the United States who received their first solid organ transplant from 1994 to 2005 (N = 210 763) u
52 tions have been shown to dramatically affect solid organ transplant graft survival in both human and
53 measurements as infection risk markers after solid organ transplant has not been fully investigated.
54 noninvasive methods to diagnose rejection in solid-organ transplants has been rejuvenated by recent o
60 partners, bridges research in the fields of solid organ transplant, hematopoietic cell transplant, a
61 lant failure or rejection (HR 3.2), previous solid organ transplant (HR 1.7), and several comorbiditi
62 duction and maintenance immunosuppression in solid organ transplants, including whole pancreas and ki
63 city and positive predictive value for other solid-organ transplants increased to 92.9% and 62.5%, re
64 ctious disease consultation in recipients of solid organ transplant is associated with increased LOS
66 ere sepsis in immunosuppressed recipients of solid-organ transplants is associated with a high mortal
67 nly associated with poor outcome after other solid organ transplants, it has not been studied in deta
68 thritis (n = 97), hematopoietic stem-cell or solid organ transplant (n = 26), or a general cohort of
69 deficiency virus coinfection, renal disease, solid-organ transplant, neuropyschiatric disease, autoim
71 erval, 1.1-14, P = 0.04), while preadmission solid organ transplant (odds ratio, 0.37; 95% confidence
73 sed by Nocardia thailandica in a 66-year-old solid organ transplant patient from Connecticut, which w
76 unoglobulin was identified in only 3% of all solid organ transplant patients pretransplant (n=34).
77 ill, oncologic or stem cell transplant, and solid organ transplant patients showed a relationship be
78 4 expression by cryptococcal strains from 24 solid organ transplant patients was associated with diss
81 We studied six cases of CMV replication in solid organ transplant patients whose genotypic testing
84 (Carbapenem-Resistant Enterobacteriaceae in Solid Organ Transplant Patients) has provided pivotal da
91 ed all cryptosporidiosis cases identified in solid organ transplanted patients between 2006 and 2010
93 trated efficacy in preventing CMV disease in solid-organ transplant patients as well as congenital di
94 ional markers aimed at identifying long-term solid-organ transplant patients at high risk of developi
95 We assessed kidney function and histology in solid-organ transplant patients during HEV infection.
96 24% of Cryptococcus neoformans isolates from solid-organ transplant patients exhibited altered sensit
97 strategy to prevent infection and disease in solid-organ transplant patients has not been evaluated b
99 th significant morbidity and mortality among solid-organ transplant patients, but approaches to diagn
102 g transplantation lags behind that for other solid organ transplants, primarily because of allograft
103 d trials and experience from other pediatric solid organ transplant recipient populations will contin
104 topathologic abnormalities are common in the solid organ transplant recipient with diarrhea, the find
106 even patients (10 with HIV infection and one solid-organ transplant recipient) developed tuberculosis
110 dverse outcomes are cytomegalovirus (CMV) in solid organ transplant recipients (causing rejection), C
113 The increased incidence of skin cancers in solid organ transplant recipients (OTR) has been well es
114 reported an increased risk of skin cancer in solid organ transplant recipients (OTRs), no study has e
115 ntibody response to the 2009-H1N1 vaccine in solid organ transplant recipients (SOTR) and its clinica
116 s on the use of generic immunosuppression in solid organ transplant recipients (SOTR) based on a revi
121 view available data on coccidioidomycosis in solid organ transplant recipients and candidates seeking
122 e multiple risk factors for CNS processes in solid organ transplant recipients and establishes a time
124 excess risk are similar to those observed in solid organ transplant recipients and patients with auto
125 tion of pretransplantation HLA antibodies in solid organ transplant recipients and, in particular, th
130 n addition, a significant number of nonrenal solid organ transplant recipients develop chronic kidney
133 ssociated cluster of febrile illness among 3 solid organ transplant recipients from a common donor.
135 TICIPANTS: Cohort study using linked data on solid organ transplant recipients from the US Scientific
141 nervous system (CNS) cryptococcal lesions in solid organ transplant recipients have not been fully de
142 ntified a Swedish population-based cohort of solid organ transplant recipients in the National Patien
143 ecipients, which contains information on all solid organ transplant recipients in the United States,
146 eatment outcomes during CMV infection in 291 solid organ transplant recipients receiving valganciclov
147 ction in almost all reported cases of GBS in solid organ transplant recipients suggest that CMV may h
148 ng Enterobacteriaceae and CRE carriage among solid organ transplant recipients to inform management o
149 Treatment failure or relapse is common in solid organ transplant recipients treated for cytomegalo
150 cancer was assessed among 118,440 Caucasian solid organ transplant recipients using multivariate Cox
155 ates that elevated osteoprotegerin levels in solid organ transplant recipients with CMV infection may
156 Patients were derived form a cohort of 122 solid organ transplant recipients with cryptococcosis in
158 75] days before ICU admission), 4 (10%) were solid organ transplant recipients, and 10 (27%) were inf
159 view the current status of CMV resistance in solid organ transplant recipients, and provide diagnosti
161 most common opportunistic viral infection in solid organ transplant recipients, is associated with su
162 erebral vasculature that occurs in 0.5-5% of solid organ transplant recipients, most commonly associa
164 ctivation can cause significant morbidity in solid organ transplant recipients, particularly BK virus
165 hough diarrhea is a frequent complaint among solid organ transplant recipients, the contribution of i
166 tors for invasive mold infections among 1101 solid organ transplant recipients, thereby strengthening
168 er phase II trial, 152 treatment-naive adult solid organ transplant recipients, with CD20(+) PTLD unr
169 D) is an increasingly important diagnosis in solid organ transplant recipients, with rising incidence
204 ant strains was examined in a large group of solid organ transplant recipients; drug-resistant CMV wa
206 umatoid arthritis (n = 199), 9.0 to 20.0% in solid-organ transplant recipients (n = 197), 0% to 5.8%
211 0 fresh CMV DNA-positive plasma samples from solid-organ transplant recipients (SOTRs) were tested.
212 oad after preemptive therapy with VGCV in 22 solid-organ transplant recipients (T1/2=2.16 days), comp
213 Ad infections are a serious problem for solid-organ transplant recipients and AIDS patients as w
214 itution of antifungal therapy among non-lung solid-organ transplant recipients and helped to rule out
215 ted to occur during transitions of care, and solid-organ transplant recipients are at an increased ri
219 isted of a retrospective chart review of all solid-organ transplant recipients from 1990 to 2000.
220 he circulations of 16 asymptomatic pediatric solid-organ transplant recipients from Children's Hospit
221 ta of pandemic influenza A H1N1 infection in solid-organ transplant recipients have been described, b
222 tein-Barr Virus (EBV) infection in pediatric solid-organ transplant recipients often leads to an asym
224 e aspects that are more specific to nonrenal solid-organ transplant recipients with a focus on liver,
227 the effects of ribavirin as monotherapy for solid-organ transplant recipients with prolonged HEV vir
228 compares the present case to those of other solid-organ transplant recipients with the same infectio
229 use serious complications in bone-marrow and solid-organ transplant recipients, and current therapies
230 inhibitors, patients receiving hemodialysis, solid-organ transplant recipients, and patients with can
231 fluence susceptibility to CMV replication in solid-organ transplant recipients, particularly in patie
232 onmelanoma skin cancer is well recognized in solid-organ transplant recipients, the risk of skin canc
233 CMV) disease remains an important problem in solid-organ transplant recipients, with the greatest ris
246 er, the role of TNF-R1-mediated signaling in solid organ transplant rejection has not been defined.
248 iew is to discuss the current and historical solid organ transplant-related disruptions in the supply
249 nd long-term graft survival (like with other solid organ transplants) remains a challenge, the future
251 cause of morbidity and mortality among both solid organ transplant (SOT) and hematopoietic stem cell
252 cal and molecular pretransplant screening in solid organ transplant (SOT) donors and recipients in no
254 s a potentially fatal disorder arising after solid organ transplant (SOT) or hematopoietic stem cell
260 ic T lymphocytes (CTLs) for the treatment of solid organ transplant (SOT) recipients at high risk for
261 ecific cytotoxic T lymphocytes (EBV-CTLs) to solid organ transplant (SOT) recipients has been shown s
262 ence of invasive fungal infections (IFIs) in solid organ transplant (SOT) recipients has increased du
264 e of immune reconstitution syndrome (IRS) in solid organ transplant (SOT) recipients with cryptococco
265 We sought to determine whether a subset of solid organ transplant (SOT) recipients with high likeli
266 ical characteristics, risks, and outcomes in solid organ transplant (SOT) recipients with zygomycosis
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
278 gained over the years shows that, similar to solid organ transplants (SOT), human VCA can also develo
283 econstitution inflammatory syndrome (IRS) in solid-organ transplant (SOT) recipients are not known.
284 Immunological parameters that distinguish solid-organ transplant (SOT) recipients at risk for life
286 ding bacteremia caused by these organisms in solid-organ transplant (SOT) recipients is lacking.
288 derlying illnesses were as follows: 13 (29%) solid-organ transplant (SOT), 11 (24%) BMT, and 7 (13%)
291 tudy was to assess the periodontal status of solid-organ transplant subjects compared to systemically
292 jection, which is in sharp contrast to other solid organ transplants, such as kidney, lung, and heart
294 inking hematopoietic chimerism induction and solid organ transplant tolerance, the mechanistic requir
295 how preexisting autoreactive T cells affect solid-organ transplants under these conditions is unknow
296 ividuals with inflammatory bowel diseases or solid-organ transplants, virome dynamics in allogeneic h
298 ransplants and reduced long-term survival of solid organ transplants, we hypothesized that convention
300 Animal organs could satisfy the demand for solid organ transplants, which currently exceeds the lim
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