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1 the placebo group (one CMV; one EBV-related posttransplant lymphoproliferative disorder).
2 ft nephropathy or viral infection, including posttransplant lymphoproliferative disorder.
3 r virus (EBV)-associated disorders including posttransplant lymphoproliferative disorder.
4 cytochemistry findings are consistent with a posttransplant lymphoproliferative disorder.
5 antibody-mediated rejection, infection, and posttransplant lymphoproliferative disorder.
6 imary mediastinal B-cell, and 1 CR of 3 with posttransplant lymphoproliferative disorder.
7 plant overall, skin, solid malignancies, and posttransplant lymphoproliferative disorder.
8 nts, who also experience higher incidence of posttransplant lymphoproliferative disorder.
9 mphomas, including Burkitt lymphoma (BL) and posttransplant lymphoproliferative disorder.
10 anagement of serious EBV diseases, including posttransplant lymphoproliferative disorder.
11 with multiple human malignancies, including posttransplant lymphoproliferative disorder.
12 no evidence of cytomegalovirus infection or posttransplant lymphoproliferative disorder.
13 development of graft-versus-host disease or posttransplant lymphoproliferative disorder.
14 on, such as chronic active EBV infection and posttransplant lymphoproliferative disorders.
15 have a 45% rate of progression to late-onset posttransplant lymphoproliferative disorders.
16 pleen were also introduced to reduce risk of posttransplant lymphoproliferative disorders.
17 induced by human immunodeficiency virus, and posttransplant lymphoproliferative disorders.
18 decreased IRF-1 expression in cases of human posttransplant lymphoproliferative disorder, a malignant
19 is associated with B cell proliferation and posttransplant lymphoproliferative disorder after alloge
20 d four children in group II (7.8%) developed posttransplant lymphoproliferative disorder after conver
22 ectrum of EBV latent gene expression in most posttransplant lymphoproliferative disorders and from th
23 ession, and there was no association between posttransplant lymphoproliferative disorders and pretran
24 tt's lymphoma (BL), HIV-associated lymphoma, posttransplant lymphoproliferative disorder, and nasopha
25 ell, immunoblastic large B cell, follicular, posttransplant lymphoproliferative disorder, and periphe
26 Risk of transplant pancreatic insufficiency, posttransplant lymphoproliferative disorder, and postspl
27 notherapy, for example, renal impairment and posttransplant lymphoproliferative disorder, and the eff
32 rr virus- (EBV) related disorders, including posttransplant lymphoproliferative disorder, constitute
33 reased risk of Epstein-Barr virus-associated posttransplant lymphoproliferative disorder (EBV-PTLD) i
34 .2% at 12 months, and 99.1% of patients were posttransplant lymphoproliferative disorder-free through
35 n of other complications post-ITx, including posttransplant lymphoproliferative disorder, graft-versu
36 ipients were alive with no single example of posttransplant lymphoproliferative disorder, graft-versu
38 rus (EBV) DNAemia is a major risk factor for posttransplant lymphoproliferative disorder; however, im
39 After the diagnosis of posttransplant lymphoproliferative disorder, immunosuppr
40 iferative disorder was 10%; the incidence of posttransplant lymphoproliferative disorder in the last
43 iver failure (n=2), chronic rejection (n=3), posttransplant lymphoproliferative disorder (n=1), graft
44 deaths occurred from de novo cancer (n=13), posttransplant lymphoproliferative disorder (n=5), age-r
46 rvival and improved QALYs, without increased posttransplant lymphoproliferative disorder or cytomegal
47 urs in the context of immunosuppression (eg, posttransplant lymphoproliferative disorders or HIV [AID
48 on of the monoclonal clone or development of posttransplant lymphoproliferative disorders or other ma
49 [OR], 0.53; P <.001) but with the increased posttransplant lymphoproliferative disorder (OR, 1.75; P
50 s C virus or hepatitis B virus, disseminated posttransplant lymphoproliferative disorder, or late rej
51 wo reported cases of cyclosporine-associated posttransplant lymphoproliferative disorders presenting
52 outcome of Epstein-Barr virus (EBV)-related posttransplant lymphoproliferative disorder (PTLD) after
55 or to mortality, including two patients with posttransplant lymphoproliferative disorder (PTLD) and o
57 There were no new safety signals and no new posttransplant lymphoproliferative disorder (PTLD) cases
59 rus (EBV) and associated with development of posttransplant lymphoproliferative disorder (PTLD) follo
81 nosis of Epstein-Barr virus (EBV)-associated posttransplant lymphoproliferative disorder (PTLD) is re
82 on of immunosuppressive regimens (ISRs) with posttransplant lymphoproliferative disorder (PTLD) may b
87 ncidence of early Epstein-Barr virus-related posttransplant lymphoproliferative disorder (PTLD) was 9
90 pressants has raised the question of whether posttransplant lymphoproliferative disorder (PTLD), a co
93 children; in addition, 10 children developed posttransplant lymphoproliferative disorder (PTLD), whic
100 homa is a rare subtype of monomorphic B-cell posttransplant lymphoproliferative disorder (PTLD).
101 ost important risk factor for development of posttransplant lymphoproliferative disorder (PTLD).
102 e recently included in the classification of posttransplant lymphoproliferative disorder (PTLD).
103 as been associated with an increased risk of posttransplant lymphoproliferative disorder (PTLD).
104 an transplant recipients with EBV-associated posttransplant lymphoproliferative disorder (PTLD).
105 lassified into skin cancer, solid tumor, and posttransplant lymphoproliferative disorder (PTLD).
106 plicating withdrawal of immunosuppression in posttransplant lymphoproliferative disorder (PTLD).
107 ype of cancer with the highest incidence was posttransplant lymphoproliferative disorder (PTLD, 1.58%
108 se The Sequential Treatment of CD20-Positive Posttransplant Lymphoproliferative Disorder (PTLD-1) tri
109 10 to 406), non-Hodgkin's lymphoma including posttransplant lymphoproliferative disorder (PTLD; SIR =
116 gic differences between patients who develop posttransplant lymphoproliferative disorders (PTLD) earl
117 y was not associated with increased risk for posttransplant lymphoproliferative disorders (PTLD) in l
120 oreticular malignancies, collectively called posttransplant lymphoproliferative disorders (PTLD), eve
121 xamine the incidence of and risk factors for posttransplant lymphoproliferative disorders (PTLD).
122 children and is associated with the risk of posttransplant lymphoproliferative disorders (PTLD).
123 prior solid organ transplantation (SOT) and posttransplant lymphoproliferative disorders (PTLD).
124 mals with prolonged graft survival developed posttransplant lymphoproliferative disorders (PTLD).
125 was plagued with high risk of rejection and posttransplant lymphoproliferative disorders (PTLD).
126 tion (BMT) is linked to an increased risk of posttransplant lymphoproliferative disorders (PTLD); how
127 The genetic mechanisms that give rise to posttransplant lymphoproliferative disorders (PTLDs) are
132 of lymphomas, but knowledge of their role in posttransplant lymphoproliferative disorders (PTLDs) is
136 munosuppressive agents foster development of posttransplant lymphoproliferative disorders (PTLDs), th
137 expressed in the majority of EBV-associated posttransplant lymphoproliferative disorders (PTLDs).
138 is also a known factor in the development of posttransplant lymphoproliferative disorder (PTLPD) in a
139 inhibitors (tacrolimus or cyclosporine) and posttransplant lymphoproliferative disorders related to
146 cytomegalovirus disease was 13%, and that of posttransplant lymphoproliferative disorder was 10%; the
148 skin, solid posttransplant malignancies, and posttransplant lymphoproliferative disorder were 3.2 (1.
151 omes, including opportunistic infections and posttransplant lymphoproliferative disorder, were studie
152 ugh plasma cell neoplasms are a rare form of posttransplant lymphoproliferative disorder, which could
153 recipient who developed relapsed/refractory posttransplant lymphoproliferative disorder with CD19-di