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1 quired immune deficiency states (e.g., after organ transplantation).
2 se of weight limits (ie, orthopedic surgery, organ transplantation).
3 treating hypoxic-ischemic human diseases and organ transplantation.
4 ted rejection and graft loss after all solid organ transplantation.
5 lograft survival and unmet clinical needs in organ transplantation.
6 he main obstacle in the long-term success of organ transplantation.
7 risk of skin cancer, particularly SCC, after organ transplantation.
8 A) is recommended in patients awaiting solid organ transplantation.
9 immunodeficiency virus (HIV)-caused AIDS and organ transplantation.
10 ental illness (SMI) a significant concern in organ transplantation.
11 enge limiting allograft survival after solid organ transplantation.
12  in myocardial infarction, stroke, and solid organ transplantation.
13 incidence of cancer is increased after solid organ transplantation.
14 gnificant role in graft survival after solid organ transplantation.
15 ytomegalovirus (CMV) replication after solid organ transplantation.
16 r controlling antibody-mediated rejection in organ transplantation.
17 ation, remains the major problem in clinical organ transplantation.
18 olved in post-I/R injuries as observed after organ transplantation.
19 infrequent but serious complication of solid organ transplantation.
20  been widely used to prevent rejection after organ transplantation.
21 ion of nitric oxide inhibition reduce IRI in organ transplantation.
22 Diarrhea is a frequent complication of solid organ transplantation.
23 t survival is a major challenge facing solid organ transplantation.
24 iseases and to prevent graft rejection after organ transplantation.
25 t important cutaneous complication following organ transplantation.
26 allograft injury and improve the outcomes of organ transplantation.
27 gs is one of the key research goals in solid organ transplantation.
28 ut allergy has been reported following solid organ transplantation.
29 s to allografts represent a major barrier in organ transplantation.
30 atopoiesis and to induce tolerance for solid organ transplantation.
31 ajor source of morbidity and mortality after organ transplantation.
32 DQ antigens and antibodies are evaluated for organ transplantation.
33 mpromised patients, particularly after solid organ transplantation.
34 he case of therapeutic immunosuppression for organ transplantation.
35 ch as IPoC can improve the outcomes of human organ transplantation.
36 therapeutic agents to improve the outcome of organ transplantation.
37 and immune control of replication post-solid organ transplantation.
38 e effect of aging and the immune response to organ transplantation.
39 hodology to reposition FDA approved drugs in organ transplantation.
40 phic variation in CMV management after solid organ transplantation.
41 tation monitoring of HLA antibodies in solid organ transplantation.
42  and substance abuse in the context of solid-organ transplantation.
43 cause of mortality and morbidity after solid organ transplantation.
44 d can mediate immune tolerance to subsequent organ transplantation.
45 imary cause of long-term graft failure after organ transplantation.
46 osis (ALS) are a viable source of tissue for organ transplantation.
47 HHV) are exacerbated by immunosuppression in organ transplantation.
48 s, it has received little attention in solid organ transplantation.
49 may also be associated with PRES after solid organ transplantation.
50 tis and can be transmitted through tissue or organ transplantation.
51 l research, tissue engineering research, and organ transplantation.
52 ansplantation, autoimmune disease, and solid organ transplantation.
53  (UNOS) and outcomes were compared to single-organ transplantation.
54 ly applicable refinement of Treg therapy for organ transplantation.
55 g therapy and their therapeutic potential in organ transplantation.
56    Skin cancer is a frequent complication of organ transplantation.
57 de in improving short-term outcomes in solid organ transplantation.
58 timal agent for tolerance induction in human organ transplantation.
59 s a well-recognized complication after solid-organ transplantation.
60 have raised concerns about medical errors in organ transplantation.
61 a common opportunistic infection after solid organ transplantation.
62 ased age, white race, male sex, and thoracic organ transplantation.
63 (IRI) remains unresolved problem in clinical organ transplantation.
64 he use of CD154 as a peripheral biomarker in organ transplantation.
65 ward personalized and predictive medicine in organ transplantation.
66 ut challenging type of rejection after solid organ transplantation.
67 d outcomes of colectomy for CDAD after solid organ transplantation.
68 d cancer, and to prevent rejection following organ transplantation.
69 eal transplantation is the most common solid organ transplantation.
70 s the most common malignancy occurring after organ transplantation.
71  improve chronic CNI nephrotoxicity in solid organ transplantation.
72 ion of cytomegalovirus (CMV) is essential in organ transplantation.
73 ne of the most common infections after solid organ transplantation.
74 n the cellular and humoral response in solid organ transplantation.
75 oses of immunosuppression is a major goal in organ transplantation.
76 rder (PTLD) is a major complication of solid-organ transplantation.
77  pediatric with EBV (+) PTLD following solid-organ transplantation.
78 s cell biology, tissue engineering, and cell/organ transplantation.
79 als as a potential therapy in cell and solid organ transplantation.
80 henolate sodium, and it is widely used after organ transplantation.
81 matching improves graft survival rates after organ transplantation.
82  25-30 times greater in CF patients after an organ transplantation.
83 ng the organ supply/demand mismatch in solid organ transplantation.
84 s in HLA antibody responses and matching for organ transplantation.
85  regarding the use of social media to foster organ transplantation.
86 g those associated with bone marrow or solid organ transplantation.
87 ns of reducing allograft rejection following organ transplantation.
88 les in ocular surface immunity and allogenic organ transplantation.
89 s and opportunities in contemporary clinical organ transplantation.
90 s and solutions to the current challenges in organ transplantation.
91 ent and its effect on the immune response to organ transplantation.
92 potential uses of nanotechnology in cell and organ transplantation.
93 fted tissues are the major reason for failed organ transplantation.
94 , prenatal diagnosis, infectious diseases or organ transplantation.
95 ns of this novel MPS classification in solid organ transplantation.
96 tions for this malignancy-tumor resection or organ transplantation.
97 patients who are not considered eligible for organ transplantation.
98 outcomes associated with smoking after solid organ transplantation.
99 HHV-8)-related disease described after solid organ transplantation.
100 fter allogeneic hematopoietic cell and solid organ transplantation.
101 tious diseases, and it has also been used in organ transplantation.
102 ful monitoring tool in cancer, pregnancy and organ transplantation.
103  provides an alternative pathway to deceased organ transplantation.
104 cess of ischemia-reperfusion injury (IRI) in organ transplantation.
105 itions but has only recently been applied to organ transplantation.
106  is improving long-term outcomes after solid organ transplantation.
107 tems have successfully been applied in solid organ transplantations.
108 g transplantation are the lowest among solid organ transplantations.
109 50%, which is far behind that of other solid organ transplantations.
110 e prospective multicenter Clinical Trials in Organ Transplantation-04 study.
111                       The Clinical Trials in Organ Transplantation-09 Trial was a randomized, prospec
112 ated factors (hospital with <800 beds, solid organ transplantation activity, higher annual incidence
113 rrent immunosuppressive therapies applied to organ transplantations affect the wide array of Treg pop
114                                              Organ transplantation after cardiopulmonary resuscitatio
115                        Pregnancy after solid organ transplantation, although considered high risk for
116 ew discusses the nature of these triggers in organ transplantation and also potential mediators that
117  of specialized health care services such as organ transplantation and bariatric surgery is advocated
118 f a complex diagnosis especially after solid organ transplantation and can lead to difficulties in fi
119 l stem cells as a therapeutic agent in solid organ transplantation and emphasizes the issues (proper
120 rus (CMV) is the most common infection after organ transplantation and has a major impact on morbidit
121 imilar to those usually reported after solid organ transplantation and have prompted different strate
122  the prevention and treatment of TB in solid organ transplantation and hematopoietic stem cell transp
123 about the T cell response because it governs organ transplantation and hinders the discovery of disea
124 immunocompromised patients, in particular in organ transplantation and in stem cell therapy.
125 er used worldwide to evaluate the success of organ transplantation and is especially feasible after r
126  are common and may lead to a need for solid-organ transplantation and may also contribute to signifi
127 periocular region represents a risk of solid organ transplantation and may produce significant ocular
128      The disparity between patients awaiting organ transplantation and organ availability increases e
129 nhibitors (CNIs) revolutionized the field of organ transplantation and remain the standard of care 40
130 therapies to modulate the immune response in organ transplantation and repair tissues after acute or
131                               The demand for organ transplantation and repair, coupled with a shortag
132 iciency virus (HIV)-positive persons seeking organ transplantation and serving as organ donors for HI
133 VCA retrieval and transplantation is akin to organ transplantation and should be incorporated into th
134 to oral calcineurin inhibitors used in solid-organ transplantation and spontaneous reporting of malig
135 ption of a pathogenic role for NETs in solid organ transplantation and suggest that NETs are a promis
136 65 years are referred for and have access to organ transplantation, and an increasing number of older
137 hma, autoimmune diseases, tumor development, organ transplantation, and chronic infections during the
138 ver disease, lung disease, malignancy, other organ transplantation, and human immunodeficiency virus
139 njury (IRI) is common in general surgery and organ transplantation, and in the case of liver, it trig
140 e rejection remains a significant problem in organ transplantation, and lymphatic and blood vessels a
141 g from smoking cessation and healthy diet to organ transplantation, and most of all condemnation of h
142 irreversible end-stage organ failure undergo organ transplantation, and organs from obese donors are
143 revalent infectious complication after solid organ transplantation, and recipients of isolated intest
144  influenced by cardiovascular disease, other organ transplantation, and the total comorbidity scores.
145 cause of diabetic ketoacidosis, neutropenia, organ transplantation, and/or increased serum levels of
146    Cancer incidence is different among solid organ transplantations, and ratios may be higher than th
147                       The Clinical Trials in Organ Transplantation Antibody Core Laboratories investi
148 rms of routine exercise training after solid organ transplantation are unclear.
149 ene (1349/1350 nucleotides), thus confirming organ transplantation as the route of transmission.
150 s, including those for bone marrow and solid organ transplantation, autoimmune diseases, and tissue a
151 opoietic stem cell transplantation, or solid organ transplantation be screened for active or prior he
152     A total of 3489 patients underwent solid organ transplantation between 1990 and 2008.
153 shed with subject headings relating to solid organ transplantation between August 1, 2011, and July 3
154 ompted by the recent completion of the first organ transplantation between HIV-infected persons in Ca
155 nt demonstration of the short term safety of organ transplantation between HIV-infected persons promp
156 is of adult patients who underwent abdominal organ transplantation between January 1, 2008, and Decem
157 t public health measures associated with the organ transplantation, beyond those already in place.
158 ed with morbidity and mortality in abdominal organ transplantation but has not been examined in lung
159                      In the setting of solid-organ transplantation, calcineurin inhibitor (CNI)-based
160                Women with a history of solid-organ transplantation can be safely offered a wide range
161                 Although desensitization for organ transplantation carries an increased risk of antib
162           The study was conducted in a large organ transplantation center that serves the entire Norw
163 ons in the treatment of autoimmune diseases, organ transplantation, chronic infection, and cancer.
164 llergy, asthma, autoimmune diseases, tumors, organ transplantation, chronic infections, and pregnancy
165 ed for randomized controlled trials in solid organ transplantation comparing an mTOR-I with a non-mTO
166 reatment of cytomegalovirus disease in solid organ transplantation, confirmed genotypic drug resistan
167 wever, the number of patients awaiting solid organ transplantation continues to remain much higher th
168 undergoing immunosuppression following solid organ transplantation, contributing substantially to mor
169 itioning for tolerance induction until after organ transplantation could further decrease the efficac
170 pported by the NIH-funded Clinical Trials in Organ Transplantation (CTOT) Consortium.
171 withdrawal (ITN030ST) and Clinical Trials in Organ Transplantation (CTOT-03) studies.
172 at led to the multicenter Clinical Trials in Organ Transplantation (CTOT-04) study and the discovery
173  sepsis (CV = 1.37) and among the lowest for organ transplantation (CV </= 0.43).
174 PTLD or chronic high viral loads after solid organ transplantation exhibited no homogeneous EBV gene
175         T cell depletion is commonly used in organ transplantation for immunosuppression; however, a
176 Cell therapies are potential alternatives to organ transplantation for liver failure or dysfunction b
177 ions on necessary future studies to optimize organ transplantation for older people.
178 tely, will not consider manuscripts on human organ transplantation for publication unless appropriate
179 t common infectious complication after solid organ transplantation, frequently affecting the gastroin
180                                              Organ transplantation from ABO blood group-incompatible
181                  Existing legislation allows organ transplantation from an HIV-infected donor under e
182 y review considerations related to advancing organ transplantation from HIV-infected donors in Canada
183 em cell transplant cohort and excluded solid-organ transplantation from this cohort.
184              HIV-infected persons undergoing organ transplantation generally achieve comparable patie
185                         The Saudi Center for Organ Transplantation has been established in 1985 as a
186                                Their role in organ transplantation has been poorly defined due to con
187                        The risk of SCC after organ transplantation has declined significantly since t
188      Emerging knowledge regarding B cells in organ transplantation has demonstrated that these cells
189 gh short-term allograft survival after solid organ transplantation has improved during the past two d
190  biomarkers of acute rejection (AR) in solid organ transplantation have been addressed in multiple sm
191  mechanisms of colorectal carcinoma in solid organ transplantation have not been well characterized.
192 Current immunosuppression regimens for solid-organ transplantation have shown disappointing efficacy
193 is exceptionally high for all patients after organ transplantation; however, predictors of the HRQoL
194 ntibody can be a major barrier to successful organ transplantation; however, therapy to control antib
195 se of a novel procedure called ischemia-free organ transplantation (IFOT) for patients with end-stage
196                                  After solid organ transplantation, immune-mediated rejection mandate
197 cytomegalovirus (CMV) management after solid organ transplantation in 2010, which provide recommendat
198 e oral cavity, which may develop after solid organ transplantation in children.
199 he National Institutes of Health (NIH) Solid Organ Transplantation in HIV Trial, reflecting experienc
200 ent of India has established laws to conduct organ transplantation in India.
201 cohort study of patients who underwent solid-organ transplantation in Ontario, Canada, between 1991 a
202 produced functional bioengineered livers for organ transplantation in preclinical studies.
203                                              Organ transplantation in the KSA has made great strides
204 n, introduced in 2013, will further increase organ transplantation in the UK.
205  donor-derived HTLV-1-associated death after organ transplantation in the world.
206 T-cell responses occurring in mismatched HLA organ transplantation in which the drug in effect create
207  treatment may improve recipient outcomes in organ transplantation; in this analysis, we aimed to det
208  numerous immunomodulatory therapies used in organ transplantation, including depletional antibody in
209                       Studies in other solid-organ transplantations indicate that low levels of serum
210  significant source of late graft loss after organ transplantation.Induction of mixed hematopoietic c
211 one of immunosuppressive therapy after solid organ transplantation, inhibits calcineurin activation.
212                                              Organ transplantation into sensitized patients with pree
213                                        Solid organ transplantation is a curative therapy for hundreds
214           The high risk of skin cancer after organ transplantation is a major clinical challenge and
215 ndary to infectious aortitis following solid organ transplantation is a rare event that in the absenc
216          Immunosuppression therapy following organ transplantation is a significant factor in the dev
217                                              Organ transplantation is a victim of its own success.
218                                        Solid organ transplantation is a vital therapy for end stage d
219                                     Although organ transplantation is an effective therapy for older
220                                              Organ transplantation is an eminent case in which the ev
221     Cytomegalovirus (CMV) infection in solid-organ transplantation is associated with increased morbi
222     Acute kidney injury after nonrenal solid organ transplantation is associated with prolonged lengt
223 ocyte antigen (HLA) class I antibodies after organ transplantation is associated with subsequent acut
224                                        Solid organ transplantation is encumbered by an increasing num
225           Its use as an induction therapy in organ transplantation is increasing.
226  but the role of the innate immune system in organ transplantation is just emerging.
227 -stage chronic kidney disease, the option of organ transplantation is limited because of the scarce a
228                      ABO-incompatible (ABOi) organ transplantation is performed owing to unremitting
229                             Saudi Center for Organ Transplantation is playing a central role in all a
230     The role of natural killer (NK) cells in organ transplantation is poorly understood because studi
231                                              Organ transplantation is the most successful treatment f
232                                        Solid organ transplantation is the preferred treatment for pat
233                           The field of solid organ transplantation is unique in the breadth of the st
234  of generic immunosuppressive drugs in solid organ transplantation is warranted.
235 wine influenza could be transmitted by solid organ transplantation led to the publication of guidance
236                                    Following organ transplantation, lifelong immunosuppressive therap
237            Severe B-lineage PTLD after solid organ transplantation may be classified as SR or HR and
238 xperience in developing the laws that govern organ transplantation may be of value for others underta
239 plotype B from viral replication after solid organ transplantation may extend beyond CMV to other her
240 eting of the Mesenchymal Stem Cells in Solid Organ Transplantation (MiSOT) Consortium took place in B
241 loning will bring enhanced possibilities for organ transplantation, nerve cells and tissue healing, a
242  chronic kidney disease after nonrenal solid organ transplantation (NRSOT), although there are little
243 ing strategy to induce tolerance after solid-organ transplantation or prevent graft-versus-host disea
244 an important opportunistic pathogen in solid organ transplantation, particularly in lung transplant r
245 erum samples obtained from nonselected solid-organ transplantation patients suffering from probable,
246  support exclusion of pulmonary IFI in solid-organ transplantation patients, the low positive predict
247        Current immunosuppression regimens in organ transplantation primarily inhibit T cells.
248                                     In solid organ transplantation recipients, exercise is able to im
249 have reported EBV(-) PTLD in pediatric solid-organ transplantation recipients.
250                                        Solid organ transplantation reduces both morbidity and mortali
251                            We used the Dutch Organ Transplantation Registry to include recipients (>/
252                               From the Dutch Organ Transplantation Registry, we selected 3597 recipie
253 Mitigating therapies, aside from impractical organ transplantation, remain limited and the possibilit
254 e relationship of CTLA4Ig and IDO in in vivo organ transplantation remains unclear.
255 ne of the most common infections after solid-organ transplantation, resulting in significant morbidit
256                                              Organ transplantation results in the activation of both
257 valuation in autoimmune and allogeneic solid organ transplantation settings, data supporting the immu
258                                In most solid organ transplantation settings, the role of NK cells is
259  preclinical models and experiences in human organ transplantation should allow for optimization of t
260 acteristics, and outcomes of SAB after solid organ transplantation (SOT) and compare these features w
261   Immune measurements that distinguish solid organ transplantation (SOT) recipients who control cytom
262 tion is an ongoing clinical problem in solid-organ transplantation (SOT).
263 nd mortality among patients undergoing solid organ transplantation (SOT).
264 e net state of immunosuppression after solid organ transplantation (SOT).
265 poieitc cell transplantation (HCT) and solid organ transplantation (SOT).
266 ors, in regulating the alloresponse to solid organ transplantation (SOT).
267              Incidences may vary among solid organ transplantations (SOTs) and may take to particular
268                                              Organ transplantation started in the Kingdom of Saudi Ar
269 sion as part of the NIAID Clinical Trials in Organ Transplantation Study.
270 and infectious challenges accompanying solid organ transplantation, susceptibility to post-transplant
271 icle, we will consider some of the topics in organ transplantation that were discussed by the attende
272 out hematologic malignancy or previous solid organ transplantation) that were collected for routine m
273                                           In organ transplantation, the composition of the B-cell com
274 prevalence of diabetes mellitus, cancer, and organ transplantation, the number of patients at risk fo
275 ch are similar to those reported after solid organ transplantation, the patient is satisfied of her n
276 s of rabies virus transmission through solid organ transplantation, there was a long incubation perio
277                     KS can develop following organ transplantation through reactivation of the recipi
278 bservation, we sought to model neonatal ABOi organ transplantation to allow mechanistic studies of to
279 extensively by investigators in the field of organ transplantation to study the rejection process, te
280 rdiac surgery with cardiopulmonary bypass or organ transplantations to reduce excessive blood loss.
281 ve helped to shape the ethical boundaries of organ transplantation today.
282                              In experimental organ transplantation, tolerance is induced by administr
283 icity because of congenital and blood and/or organ transplantation transmissions and the reactivation
284 IRI) can occur in clinical scenarios such as organ transplantation, trauma and cardio-pulmonary bypas
285 s in modern medicine, such as major surgery, organ transplantation, treatment of preterm babies, and
286                             ABO-incompatible organ transplantation typically induces hyperacute rejec
287 on-based cancer cohort, we evaluated whether organ transplantation was associated with worse prognosi
288         The SMR for cancer death after solid-organ transplantation was higher in children (SMR, 84.61
289                                        Solid-organ transplantation was identified using the national
290 ccurring in a kidney recipient shortly after organ transplantation was identified.
291               In previous decades, access to organ transplantation was restricted to academic medical
292       The relevance of this pathway to solid-organ transplantation was then confirmed by the demonstr
293 n, haematological malignancies, and previous organ transplantation were excluded).
294 xciting advances in the clinical sciences in organ transplantation were presented at the American Tra
295                                 Unlike solid organ transplantation, which is potentially life-saving,
296        Balamuthia can be transmitted through organ transplantation with an observed incubation time o
297 ow) regulatory T cells (Tregs) in a model of organ transplantation with CD40Ig could be abrogated by
298  and everolimus, are increasingly used after organ transplantation with potential advantages in virus
299       Seventy-four cases of PTLD after solid organ transplantation with sufficient material for furth
300 virus (HTLV)-1 has been reported after solid-organ transplantation, with a related fatal outcome in l

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