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1 es them impractical for surgical removal and autologous transplantation.
2 of patients with germ cell tumors undergoing autologous transplantation.
3 patients received melphalan 200 mg/m(2) with autologous transplantation.
4 tic syndromes (MDS) have been reported after autologous transplantation.
5  sufficient numbers of normal stem cells for autologous transplantation.
6 n chemotherapy and three after allogeneic or autologous transplantation.
7 amyloidosis who meet functional criteria for autologous transplantation.
8 normal PBSCs could be collected and used for autologous transplantation.
9 tute the hematopoietic compartment following autologous transplantation.
10 ocytic cells resistant to HIV-1 growth after autologous transplantation.
11 tation or use of ANK to purge CML marrow for autologous transplantation.
12  of pulp-dentin regeneration in vivo through autologous transplantation.
13 C expansion and lineage commitment following autologous transplantation.
14 rative medicine, given their feasibility for autologous transplantation.
15  prognostic impact of del(13) observed after autologous transplantation.
16 ration as consolidation therapy after double autologous transplantation.
17 cal to validate their in vivo fate following autologous transplantation.
18  experienced treatment failure with previous autologous transplantation.
19 plications, as these cells could be used for autologous transplantation.
20  tiuxetan was followed by high-dose BEAM and autologous transplantation.
21 ted with rituximab-induced neutropenia after autologous transplantation.
22 ed DLBCL should be considered for RIT versus autologous transplantation.
23 reviously experienced treatment failure with autologous transplantation.
24 ized to chemotherapy for 2.5 years versus an autologous transplantation.
25 was administered a median of 3 months before autologous transplantation.
26 ived allogeneic marrow and one had undergone autologous transplantation.
27 bination of ex vivo genetic manipulation and autologous transplantation.
28  who experience disease recurrence following autologous transplantation.
29 ts (56%) entered into the study proceeded to autologous transplantation.
30   There may be a benefit to graft purging in autologous transplantation.
31 worse for those who had previously undergone autologous transplantation.
32 3, and 48% of patients had undergone a prior autologous transplantation.
33 cies, and ex vivo purging of cancer cells in autologous transplantation.
34 ransplantations, whereas 162 (99%) performed autologous transplantations.
35  of intensive chemotherapy (117 patients) or autologous transplantation (115 patients).
36 her 5-year OS (46%) than those randomized to autologous transplantation (37%; P = .03).
37 remission therapies: intensive chemotherapy, autologous transplantation (ABMT), or allogeneic bone ma
38                                    Following autologous transplantation, all three patients exhibited
39                                Compared with autologous transplantation, allogeneic PBPC transplantat
40 allogeneic transplantation (auto/RICallo) to autologous transplantation alone (auto).
41 arrow function is similar to that seen after autologous transplantation and does not carry the risk f
42  be safely combined with high-dose BEAM with autologous transplantation and has the potential to be m
43 ing the potential utility of these cells for autologous transplantation and possible diagnostic testi
44 pse after disease recurrence following prior autologous transplantation, and 51 patients at high risk
45                              Allogeneic SCT, autologous transplantation, and consolidation chemothera
46 l transplantation, tumor cell purging before autologous transplantation, and ex vivo cultures used fo
47 tal of 36 patients were studied (29 received autologous transplantation, and seven received allogenei
48 g as the graft of choice in many centers for autologous transplantation, and with increasing frequenc
49              High-dose melphalan followed by autologous transplantation appears effective for improvi
50                                              Autologous transplantation appears to offer a modest sur
51 ith A + G had at least a 90% success rate of autologous transplantation as assessed by neutrophil eng
52 conventional chemotherapy support the use of autologous transplantation as salvage therapy if such pa
53 it from early treatment intensification with autologous transplantation, as indicated by the possibil
54 therapy and would not have been eligible for autologous transplantation at most centers.
55 d one (n = 13) or two or more (n = 17) prior autologous transplantations (ATs).
56 nts who were treated uniformly with a tandem autologous transplantation-based protocol and were evalu
57 ecome the preferred source of stem cells for autologous transplantation because of the technical adva
58         We conclude that both allogeneic and autologous transplantation can induce durable remissions
59                                              Autologous transplantation can prolong event-free and po
60                                              Autologous transplantation can prolong overall survival
61           There is no evidence that a single autologous transplantation can replace consolidation/mai
62 ant event-free survival advantage to upfront autologous transplantation compared with interferon main
63 erived haematopoietic stem cells followed by autologous transplantation could be used to cure beta-ha
64 eed for rapid disease control, candidacy for autologous transplantation, cytopenias, IgM-related comp
65   Only the four patients treated after prior autologous transplantation developed acute GVHD (P =.000
66                                        Prior autologous transplantation failed in five (28%) patients
67 y pure populations of CD34+ marrow cells for autologous transplantation feasible.
68                                              Autologous transplantation followed by treatment with CT
69 eukemic stem cells that may be beneficial in autologous transplantation for CML and perhaps other leu
70 e prove to be an extremely useful adjunct in autologous transplantation for CML.
71 les from 12 patients who developed TMN after autologous transplantation for Hodgkin lymphoma or non-H
72 focuses on recent advances in allogeneic and autologous transplantation for mantle cell lymphoma.
73 , from $36 000 to $88 000 (USD) for a single autologous transplantation for the initial hospitalizati
74  the chemotherapy group as compared with the autologous-transplantation group was 0.81 (P = 0.20 by t
75  as compared with 38 +/- 6.4 percent for the autologous-transplantation group; and the relative risk
76 ymphoma who experience a recurrence after an autologous transplantation has been considered a hazardo
77 reduce relapse of non-Hodgkin lymphoma after autologous transplantation have included ex vivo stem ce
78 an of five lines of prior therapy, including autologous transplantation in 69%, and 17% of patients w
79 ontribute to multilineage repopulation after autologous transplantation in a clinically relevant larg
80 dopamine neurons for up to 2 years following autologous transplantation in a Parkinson's disease (PD)
81 rgue that CD44 blockade may be beneficial in autologous transplantation in CML.
82 Particular emphasis is placed on the role of autologous transplantation in first complete remission,
83 dies comparing allogeneic transplantation to autologous transplantation in multiple myeloma is few an
84                To improve survival of tandem autologous transplantation in multiple myeloma, the seco
85                                              Autologous transplantation in myeloma can prolong surviv
86 te the outcome of high-dose chemotherapy and autologous transplantation in patients with diffuse B-ce
87 ell (PBC) rescue has become the mainstay for autologous transplantation in patients with lymphoma, mu
88 primitive progenitors to hematopoiesis after autologous transplantation in the rhesus macaque model.
89 tem cells in up to 10% of donors, precluding autologous transplantation in those donors or substantia
90 use of a short consolidation treatment after autologous transplantation increases the complete respon
91                                              Autologous transplantation is increasingly used to treat
92 rrow (BM), followed by ex vivo expansion for autologous transplantation may be less morbid, and more
93 om had progression of disease after previous autologous transplantation (median age 32 years [range 1
94 ended our observations to a nonhuman primate autologous transplantation model.
95                                     Although autologous transplantation obviates the risk of graft-ve
96                                              Autologous transplantation of 10(7) NA/CD31+ MNCs, 10(7)
97                                              Autologous transplantation of bone marrow stem cells tha
98 itical aspects of vascular repair, including autologous transplantation of bone marrow-derived stem c
99 ironment poses additional challenges for the autologous transplantation of cells.
100                                              Autologous transplantation of conjunctiva and limbus are
101                        Here we show that the autologous transplantation of EGCs into the brain of Abe
102 key that developed T-cell lymphoma following autologous transplantation of enriched bone marrow stem
103 replacement therapy (ERT) is withheld before autologous transplantation of gamma-retroviral vector-tr
104 logeneic HSCT from CCR5-deficient donors and autologous transplantation of genetically modified hemat
105           In search for a better therapy, an autologous transplantation of hematopoietic progenitor c
106                                              Autologous transplantation of hematopoietic stem and pro
107 tients receiving high dose chemotherapy with autologous transplantation of hematopoietic stem cell pr
108 ere is considered to be a high potential for autologous transplantation of human dental pulp stem cel
109 ctions of impaired IP-DPSCs, suggesting that autologous transplantation of IFN-gamma-accelerated IP-D
110 st that an HIV vaccine might be delivered by autologous transplantation of in vitro-programmed HSPCs,
111           In this study, we report the first autologous transplantation of iPSCs in a large animal mo
112 underwent total body irradiation followed by autologous transplantation of marrow CD34 cells.
113 contribute to HIV cure through allogeneic or autologous transplantation of naturally occurring or eng
114 proach shows definitive engraftment by using autologous transplantation of noninjured recipients, our
115 total pancreatectomy were candidates for the autologous transplantation of pancreatic islet.
116                                              Autologous transplantation of patient-specific induced p
117 py has been developed as a method to perform autologous transplantations of a patient's own stem cell
118 cells (HSPCs) from FA patients, either after autologous transplantation or infusion into immunodefici
119 ent anti-inflammatory protocols for clinical autologous transplantation (P < 0.01).
120 al (P = .04) and specifically benefited from autologous transplantation (P = .006).
121 ing in 1994, based on encouraging results in autologous transplantation, patients (n = 81) were treat
122                The results of allogeneic and autologous transplantation preparative regimens, includi
123 patient cost in 1997 dollars was $55,500 for autologous transplantation (range, $28,200 to $148,200)
124 ped leukemia at an average of 16 months post-autologous transplantation (range, 11 to 21 months).
125 loma refractory to standard chemotherapy and autologous transplantation received a matched unrelated
126                                              Autologous transplantation should be considered in young
127  closer to their use in disease analysis and autologous transplantation strategies.
128 sing parameters derived from the analysis of autologous transplantation studies in glucose-6-phosphat
129                                              Autologous transplantation studies in non-human primates
130 imulation were applied to limiting-dilution, autologous-transplantation studies in cats heterozygous
131                           In a retrospective autologous transplantation study conducted on 706 patien
132 ercent, P = 0.005) in the group treated with autologous transplantation than in the intensive-chemoth
133 e a potential source of expandable cells for autologous transplantation to treat Parkinson's Disease
134                                        Prior autologous transplantation was associated with late chim
135 tients may receive intensive chemotherapy or autologous transplantation; we undertook this randomised
136 non-Hodgkin's lymphoma who were eligible for autologous transplantation were randomized to receive r-
137 honate use, and myeloma therapy, except more autologous transplantations were performed on patients i
138 ted poor outcomes with immunochemotherapy or autologous transplantation will be important in determin
139                          Four years earlier, autologous transplantation with a higher melphalan dose
140 reated patients, 9 are currently alive after autologous transplantation with a minimum follow-up of 1
141                                              Autologous transplantation with peripheral blood stem ce
142 ute lymphoblastic leukemia (ALL) and compare autologous transplantation with standard chemotherapy.
143 cells by use of antibodies in the setting of autologous transplantation, with emphasis on the emergin
144 generating unlimited quantities of cells for autologous transplantation, with potential application i
145             We report the ability to perform autologous transplantation without blood-product support

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