戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ia purpura, and recovered after therapy with plasmapheresis.
2 ectomy plus eculizumab (n=5), in addition to plasmapheresis.
3 aving metalloprotease by plasma infusion and plasmapheresis.
4 may respond to intravenous immunoglobulin or plasmapheresis.
5 espite treatment with fresh-frozen plasma or plasmapheresis.
6 no deaths among the 13 patients who received plasmapheresis.
7 ofile of IVIg would appear to be superior to plasmapheresis.
8 lication of HIV infection and may respond to plasmapheresis.
9 sed (one of five), and one of five underwent plasmapheresis.
10 phosphamide, intravenous immunoglobulins, or plasmapheresis.
11 bserved after rituximab; no patient required plasmapheresis.
12 ith similar death-censored graft survival to plasmapheresis.
13 d retinopathy improved in all patients after plasmapheresis.
14 inal vein by laser Doppler, before and after plasmapheresis.
15 imab dose and 4 bortezomib doses preceded by plasmapheresis.
16 requiring thymoglobulin, IVIg, rituximab, or plasmapheresis.
17 s, 3 deceased), 21 of whom had pretransplant plasmapheresis.
18                  Systemic therapies included plasmapheresis (18), chemotherapy (30), blood transfusio
19 ravenous immune globulin, 3 of 4 treated and plasmapheresis, 3 of 4 treated).
20 lasmapheresis than among those who underwent plasmapheresis (50% compared with 24%; P < 0.05).
21                        Ten patients received plasmapheresis, 6 eculizumab, and 7 a combination of bot
22 llowed by a 2-week cycle on days 1-4-8-11 of plasmapheresis and 1.3 mg/m(2) bortezomib; then 0.5 mg/k
23 eracute rejection protocol applied including plasmapheresis and antithymocyte globulin treatment as w
24 essfully reversed with the implementation of plasmapheresis and cessation of clopidogrel and cyclospo
25 nimally beneficial, but after treatment with plasmapheresis and corticosteroids, she was still asympt
26 Past protocols to desensitize patients using plasmapheresis and cyclophosphamide have not been broadl
27                             We conclude that plasmapheresis and heme-albumin are of benefit in EPP co
28 ful treatment of the patient with additional plasmapheresis and heme-albumin with improvement of hepa
29                               Treatment with plasmapheresis and high-dose corticosteroids may be effe
30 ted a patient with EPP who was improved with plasmapheresis and i.v. heme-albumin before OLT.
31 techniques such as intravenous immunoglobin, plasmapheresis and immuno-adsorption.
32                        Other options include plasmapheresis and intravenous immunoglobulin (IVIg), co
33                 Perioperative treatment with plasmapheresis and intravenous immunoglobulin (IVIG), co
34                                         Both plasmapheresis and intravenous immunoglobulin may be emp
35 gated whether cyclophosphamide combined with plasmapheresis and intravenous immunoglobulins is an opt
36  significantly higher PRA, and received more plasmapheresis and IVIG at the time of transplant.
37 -blood compatible columns, double-filtration plasmapheresis and lipoprotein (a)-apheresis.
38                                              Plasmapheresis and low-dose CMV-Ig combined with traditi
39       During this time, experience with both plasmapheresis and renal replacement therapy has become
40                              Days 2-4: daily plasmapheresis and replacement of the shed plasma with 6
41 f bortezomib (1.3 mg/m(2)) over 2 weeks with plasmapheresis and rituximab.
42 cluded in a protocol involving pretransplant plasmapheresis and splenectomy at the time of transplant
43                                              Plasmapheresis and tacrolimus-mycophenolate mofetil resc
44                                              Plasmapheresis and the addition of cyclophosphamide led
45        The patient responded dramatically to plasmapheresis and the addition of high-dose corticoster
46             We used a protocol that included plasmapheresis and the administration of low-dose intrav
47 l antibodies and complement were depleted by plasmapheresis and the use of Gal alpha1-3Gal column ads
48 ter pretransplant conditioning regimen using plasmapheresis and/or intravenous immunoglobulin therapy
49 atients, for whom treatment with thymectomy, plasmapheresis, and conventional immunotherapeutic agent
50 levels and included thymoglobulin induction, plasmapheresis, and intravenous immunoglobulin in the hi
51   Immunomodulatory agents, such as steroids, plasmapheresis, and intravenous immunoglobulin, seem to
52 ol involved pretransplant immunosuppression, plasmapheresis, and low-dose intravenous immunoglobulin+
53 avenous heparin, intravenous gamma globulin, plasmapheresis, and/or antiproliferative agents.
54  Rapid diagnosis and treatment that includes plasmapheresis are critical for improved survival.
55 n we describe our center's experience with a plasmapheresis-based desensitization protocol for highly
56 des further evidence of the high efficacy of plasmapheresis-based desensitization protocols.
57  antigen antibodies (DSA) can be overcome by plasmapheresis-based strategies with some success in ren
58               In three patients who received plasmapheresis before bortezomib, plasmapheresis failed
59 ch case, the recipient had been treated with plasmapheresis before transplantation because of a posit
60 lowing two kinds of protein depletion: batch plasmapheresis (BP; n = 5) and thoracic duct drainage (T
61                                     Although plasmapheresis caused a similar reduction in alloreactiv
62  in 8 patients and were unchanged in 1 after plasmapheresis, chemotherapy, or both.
63 us renal replacement therapy, in addition to plasmapheresis, corticosteroids, cyclophosphamide, and r
64                    Treatment for HR included plasmapheresis, cyclophosphamide, and rituximab.
65 as higher in several other groups, including plasmapheresis donors (34.0%), intravenous drug users (8
66                          However, continuous plasmapheresis dramatically increased the tumor-to-backg
67                        All patients received plasmapheresis every other day with intravenous immune g
68 o received plasmapheresis before bortezomib, plasmapheresis failed to reduce DSA.
69 esensitization, after desensitization (using plasmapheresis followed by 100 mg/kg intravenous immunog
70 ts treated with alternate-day, single-volume plasmapheresis followed by low-dose cytomegalovirus (CMV
71  to October of 1998, five patients underwent plasmapheresis for PNF after other causes of immediate a
72 ee patients were treated with eculizumab and plasmapheresis for recurrent aHUS after kidney transplan
73 versity Medical Center for consideration for plasmapheresis for the presumed essential type III cryog
74 rolimus was discontinued, and treatment with plasmapheresis, fresh frozen plasma, steroids, and OKT3
75                 All recipients who underwent plasmapheresis had restoration of liver function.
76 ntravenous immunoglobulin is increasing, but plasmapheresis has not been shown to be of benefit.
77                         Intravenous heme and plasmapheresis have been proposed but not previously rep
78 ng steroids, intravenous immunoglobulin, and plasmapheresis have shown limited efficacy in IgM monocl
79            In spite of steroid treatment and plasmapheresis, his clinical status deteriorated rapidly
80                He was managed initially with plasmapheresis, hypertransfusion, and infusions of i.v.
81 ys after transplantation, which responded to plasmapheresis, i.v.IG, and rituximab.
82 efractory to aggressive treatment, including plasmapheresis, immunosuppression with prednisolone, and
83 ne to two cycles (1.3 mg/m(2) x 4 doses) and plasmapheresis in 2008 to remove HLA antibodies posttran
84 n 3, OKT3 for concurrent rejection in 3, and plasmapheresis in 5 patients.
85 ulinemia treated successfully with long-term plasmapheresis in conjunction with thalidomide and dexam
86                                  The role of plasmapheresis in liver failure and hepatic coma remains
87               This report reviews the use of plasmapheresis in primary hepatic allograft nonfunction
88 s of action, the efficacy, and the safety of plasmapheresis in rheumatic diseases demonstrates that t
89                                        After plasmapheresis in six patients with recurrences, the per
90 anisms that explain the efficacy of repeated plasmapheresis in this setting are suggested.
91  either intravenous immunoglobulin (IVIg) or plasmapheresis, in conjunction with cyclophosphamide.
92 e 3 hemolytic uremic syndrome, not requiring plasmapheresis, in two patients (6%).
93 mplement has been treated by combinations of plasmapheresis, intravenous gamma-globulin and monoclona
94 mpatible recipients, and was reversible with plasmapheresis, intravenous immunoglobulin, and increasi
95 nti-human leukocyte antigen antibodies using plasmapheresis, intravenous immunoglobulin, and rituxima
96     All had received previous treatment with plasmapheresis, intravenous immunoglobulin, and rituxima
97 , and prednisone combined with pretransplant plasmapheresis, intravenous immunoglobulin, and splenect
98 ts treated with more than four pretransplant plasmapheresis/intravenous immunoglobulin (PP/IVIg) had
99  The immunosuppressive protocol consisted of plasmapheresis/intravenous immunoglobulin infusion befor
100 fter kidney transplantation by rituximab and plasmapheresis is ambiguous.
101                                              Plasmapheresis is effective in reversing HVS-related ret
102                                              Plasmapheresis is known to reduce serum viscosity (SV) a
103 ole of corticosteroids, immune globulin, and plasmapheresis is uncertain.
104                    Combinations that include plasmapheresis, IVIG, cyclophosphamide, and rituximab ha
105 , addition of mycophenolate mofetil (MMF) or plasmapheresis (L3); and anti-CD20 (Rituximab) (L4).
106 ine A, mycophenolate mofetil, gammaglobulin, plasmapheresis, LJP 394, flaxseed oil, bindarit, anti-CD
107                                    Patients' plasmapheresis material was tested for the presence of a
108                                     Although plasmapheresis may ameliorate acute allograft disease, s
109                         The long-term use of plasmapheresis may be a well-tolerated treatment option
110                                              Plasmapheresis may have a more consistent response rate
111                   It has been suggested that plasmapheresis may improve coagulopathy and prevent blee
112 ents treated with eculizumab (n = 11) and/or plasmapheresis (n = 13) during the acute phase of HUS ha
113 venous immunoglobulins (n = 71/74; 96%), and plasmapheresis (n = 17/74; 23%).
114 ytotoxic (CDC) crossmatch (XM) pretransplant plasmapheresis, nine had positive flow cytometric (FC) X
115 o halt the progression of CAPS, but repeated plasmapheresis not only halted the condition, but it led
116 this study was to investigate the effects of plasmapheresis on HVS-related retinopathy and retinal he
117 s/arm; range, 5-23), of which, four examined plasmapheresis (one suggested benefit) and one for immun
118                           We did not rely on plasmapheresis or anti-A titer determinations.
119 teinuria that may remit after treatment with plasmapheresis or immunoadsorption.
120          C4d deposition was not treated with plasmapheresis or intravenous immunoglobulin and was not
121    Eighteen patients (78%) were treated with plasmapheresis or low-dose IVIg+rituximab; 11 (49%) with
122  medications as needed, and consideration of plasmapheresis or use of immunoadsorption column in seve
123  lowering serum suPAR concentrations through plasmapheresis, or by interfering with the suPAR-beta(3)
124                                              Plasmapheresis, or TPE, removes monoclonal antibodies, i
125                    She responded to repeated plasmapheresis over 3 years.
126  in total plasma protein concentration after plasmapheresis (p < .05).
127 apy was administered per package insert with plasmapheresis performed immediately before each bortezo
128 t regimens commonly include a combination of plasmapheresis (PL) and intravenous immunoglobulin (IVIG
129                  The comparative efficacy of plasmapheresis (PLEX) vs immunoglobulin as maintenance t
130                                              Plasmapheresis (PP) and intravenous immunoglobulin (IVIg
131 t survival of patients with AHR treated with plasmapheresis (PP) and intravenous immunoglobulin (IVIG
132                    This patient received one plasmapheresis (PP) and intravenous immunoglobulin (IVIg
133                                              Plasmapheresis (PP) has been shown to remove HLA- specif
134                                              Plasmapheresis (PP) has been used in the treatment of va
135        Predicting recurrence and response to plasmapheresis (PP) or other interventions remains probl
136 97+/-3% vs. 76+/-20%, P=NS) and after 3 IVIg/plasmapheresis (PP) treatments but lower among responder
137 nts with anti-A1 titers > or = 1:8 underwent plasmapheresis (PP).
138 been removal of donor-specific antibodies by plasmapheresis (PPH) in conjunction with intravenous imm
139 ansplant using an intravenous immunoglobulin/plasmapheresis preconditioning regimen with interleukin-
140 body-mediated rejection and graft loss using plasmapheresis preconditioning, low-dose intravenous imm
141 Apart from drastic measures such as extended plasmapheresis, pretargeting selectivity was neither sen
142                       DSAs were removed with plasmapheresis pretransplant, and patients did not routi
143         These patients underwent two to five plasmapheresis procedures during which one plasma volume
144                                              Plasmapheresis provides an effective treatment option fo
145 antibody and a more intensive posttransplant plasmapheresis regiment aimed at maintaining low levels
146         All patients treated with bortezomib/plasmapheresis resulted in a primary DSA reduction of mo
147                                              Plasmapheresis resulted in significant reductions in ser
148             Treatment interventions included plasmapheresis, resulting in functional improvement: the
149 ata indicate that proteasome inhibitors plus plasmapheresis results in prolonged reduction of HLA ant
150 erapy (steroids, intravenous immunoglobulin, plasmapheresis), second-line immunotherapy (rituximab, c
151 A median (interquartile range) of 15 (10-23) plasmapheresis sessions was administered; 13 of the subj
152                                              Plasmapheresis should be considered for symptomatic hype
153                                     Repeated plasmapheresis should be considered in the most refracto
154                                              Plasmapheresis should be used for patients with symptoma
155 cannot give a simple answer to the question: plasmapheresis-take it or leave it?
156 , intravenous immunoglobulins, cyclosporine, plasmapheresis, thalidomide, cyclophosphamide, hemoperfu
157 her among patients who were not treated with plasmapheresis than among those who underwent plasmapher
158          Pretransplant the patients received plasmapheresis three times weekly for a planned maximum
159                It is postulated that perhaps plasmapheresis, through removal of cytokines or other me
160                   Patients were treated with plasmapheresis, thymoglobulin/OKT3, and corticosteroids.
161 the failure of corticosteroid, rituximab and plasmapheresis to attenuate the rate of decline in allog
162 bbit (r) ATG can be used in combination with plasmapheresis to effectively treat antibody-mediated re
163 recipient cross-match were desensitized with plasmapheresis to permit live donor (LD) transplantation
164 Attempts to deal with this problem have used plasmapheresis to remove antibodies or high-dose pooled
165 ma IgM levels were measured before and after plasmapheresis treatment.
166 bulin cross-match-negative after one to five plasmapheresis treatments and underwent LD transplantati
167 a pretransplant conditioning regimen of four plasmapheresis treatments followed by intravenous immuno
168                 An initial short course of 5 plasmapheresis treatments improved the patient's cutaneo
169 y-four patients had a median of 2 additional plasmapheresis treatments to reach the preoperative targ
170 nts with non-antigen-specific IA, additional plasmapheresis treatments were necessary for recipient d
171 x treatments with antigen-specific IA and 12 plasmapheresis treatments, one patient with a starting i
172 us immunoglobulin therapy, a 3-day course of plasmapheresis was administered.
173                                    Moreover, plasmapheresis was associated with an unacceptably high
174                                         Once plasmapheresis was initiated, she required no further tr
175 versible hemolytic uremic syndrome requiring plasmapheresis was observed in one patient with NHL duri
176                                              Plasmapheresis was performed for severe cases (n = 10).
177                                              Plasmapheresis was planned for up to 3 months after LDLT
178 persistence of the woman's ulcers, intensive plasmapheresis was resumed and continued 3 to 4 times pe
179                         Rejections requiring plasmapheresis were found only among patients with T-pos
180 he fifth postoperative day and completion of plasmapheresis when a repeated retrospective cross-match
181 eaths occurring in patients not treated with plasmapheresis, whereas there were no deaths among the 1
182 esistant to steroids, cyclophos-phamide, and plasmapheresis who responded to the addition of anti-CD2
183 ntinuation of FK506, anticoagulation, and/or plasmapheresis with fresh-frozen plasma exchange, resolv
184 ipients continued to receive every other day plasmapheresis with intravenous immune globulin for the
185 of a desensitization protocol also involving plasmapheresis) with specimens obtained in 91 patients w
186             He was treated with steroids and plasmapheresis, with mild improvement in vision.
187  the offending antibody may be possible with plasmapheresis, without the expectation for significant

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top