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1 been shown to be as effective as intravenous pamidronate.
2  renal function before the administration of pamidronate.
3 site in men treated with both leuprolide and pamidronate.
4 ng thalidomide (THAL, 200 mg/d) with monthly pamidronate.
5  in cultures treated with the bisphosphonate pamidronate.
6  also increased in osteoblasts cultured with pamidronate.
7  controlled, randomized, nonblinded trial of pamidronate (30 mg intravenously every 3 mo) with vitami
8 ve either leuprolide alone or leuprolide and pamidronate (60 mg intravenously every 12 weeks).
9 ults of two randomized trials that evaluated pamidronate 90 mg administered intravenously every month
10                             Intravenous (IV) pamidronate 90 mg delivered over 1 to 2 hours every 3 to
11 ession fracture from osteopenia, intravenous pamidronate 90 mg delivered over at least 2 hours or zol
12 mg subcutaneously every 4 weeks, intravenous pamidronate 90 mg over no less than 2 hours, or zoledron
13  one lytic lesion received either placebo or pamidronate (90 mg) as a four-hour intravenous infusion
14 tic bone lesion were given either placebo or pamidronate (90 mg) as a two-hour intravenous infusion m
15 sumab, 120 mg subcutaneously, every 4 weeks; pamidronate, 90 mg intravenously, every 3 to 4 weeks; or
16 is directly, we injected postnatal rats with pamidronate, a bisphosphonate that reduces bone resorpti
17 of infected, reconstituted hu-SCID mice with pamidronate, a human V gamma 2V delta 2 T cell-specific
18 dy that treatment of murine macrophages with pamidronate, a second generation aminobisphosphonate, in
19                                              Pamidronate, a second-generation bisphosponate, has been
20 2H NMR measurements of side-chain 2H-labeled pamidronate, alendronate, zoledronate, and risedronate o
21                                              Pamidronate, an aminobisphosphonate, has been shown to l
22 icacy could be evaluated in 198 who received pamidronate and 179 who received placebo.
23 tment could be evaluated in 196 who received pamidronate and 181 who received placebo.
24 One hundred eighty-two patients who received pamidronate and 189 who received placebo were assessable
25 80 of 382 randomized patients, 185 receiving pamidronate and 195 receiving placebo.
26             Other bisphosphonates, including pamidronate and clodronate, seem to be ineffective in th
27  oxyalkyl, and sulfanylalkyl) derivatives of pamidronate and one alendronate, a molecular field analy
28                                              Pamidronate and other bisphosponates, used as supportive
29 ustained significant differences between the pamidronate and placebo groups in self-reported pain mea
30 nly used in bone resorption therapy, such as pamidronate and risedronate.
31 nitrogen-containing bisphosphonates, such as pamidronate and risedronate.
32 after lung transplant and improved with both pamidronate and time.
33 ng free divalent ion concentrations, whereas pamidronate and zoledronate appear to act on the hFOB ce
34                                              Pamidronate and zoledronate decreased hFOB cell prolifer
35                                         Both pamidronate and zoledronate increase hFOB cell bone form
36                           Intravenous use of pamidronate and zoledronic acid is associated with most
37 ed treatment with the potent bisphosphonates pamidronate and zoledronic acid seems to be well tolerat
38                           The choice between pamidronate and zoledronic acid will depend on choosing
39 t supports that oral clodronate, intravenous pamidronate, and intravenous zoledronic acid are superio
40 decreased with monthly infusions of 90 mg of pamidronate, and this effect was maintained for at least
41 t and prostate cancer patients (ibandronate, pamidronate, and zoledronic acid).
42 sphosphonates, particularly the potent agent pamidronate (Aredia), will relieve metastatic bone pain
43 t, the only agent common to all patients was pamidronate (Aredia).
44                      Treatment with 90 mg of pamidronate as a 2-hour intravenous infusion every 4 wee
45                         Monthly infusions of pamidronate as a supplement to chemotherapy can protect
46               Long-term monthly infusions of pamidronate as an adjunct to chemotherapy are superior t
47                                              Pamidronate at an intraperitoneal dose of 10 mg/kg/day f
48                  Patients began therapy with pamidronate at or below the recommended dose of 90 mg, i
49                                              Pamidronate-augmented TNF-alpha production by macrophage
50 ore, pretreatment of murine macrophages with pamidronate before stimulation with IFN-gamma significan
51 all-cell lung, 183; other, 168) and 362 with pamidronate (breast, 254; myeloma, 108).
52                           The bisphosphonate pamidronate decreases skeletal complications and improve
53                                  Intravenous pamidronate disodium (90 mg) or placebo was administered
54                                              Pamidronate disodium failed to demonstrate a significant
55                      Bisphosphonates such as pamidronate disodium inhibit osteoclast-induced bone res
56 the effect of an intravenous bisphosphonate, pamidronate disodium, on pain control in metastatic pros
57 s were treated with docetaxel, docetaxel and pamidronate disodium, or docetaxel and cyclophosphamide.
58 ard dosing regimen of zoledronic acid and/or pamidronate disodium.
59                                              Pamidronate does increase the size of the osteoclasts, i
60                                     However, pamidronate does not increase survival and is associated
61                                              Pamidronate does not inhibit the gene expression of the
62 hat clinicians consider reducing the initial pamidronate dose in patients with pre-existing renal imp
63 ed 9 or more doses of zoledronic acid and/or pamidronate during the first 10 to 15 months of therapy.
64 ned the effects of alendronate, risedronate, pamidronate, etidronate, and clodronate on apoptosis and
65 dronate (n = 34) or pamidronate (n = 17) and pamidronate followed by zoledronate (n = 33).
66                            Patients received pamidronate for 15 to 48 mo before presentation with ren
67                    The patients treated with pamidronate gained 8.8 +/- 2.5% and 8.2 +/- 3.8% in spin
68 eletal events was significantly lower in the pamidronate group (24 percent) than in the placebo group
69 had any skeletal complication was 56% in the pamidronate group and 67% in the placebo group (P = .027
70 ne resorption markers were suppressed in the pamidronate group compared with placebo.
71 rst skeletal complication was greater in the pamidronate group than in the placebo group (13.1 vs. 7.
72 ation of performance status (P=0.027) in the pamidronate group than in the placebo group.
73  of skeletal events per year was less in the pamidronate-group (1.3) than in placebo-treated patients
74 eveloped any skeletal event was lower in the pamidronate-group (P = .015).
75 nd six fractures occurred in the control and pamidronate groups, respectively (p > 0.2).
76                    The patients who received pamidronate had significant decreases in bone pain and n
77  synthase inhibitors, such as risedronate or pamidronate, had little or no activity.
78 ogen-containing bisphosphonates alendronate, pamidronate, homorisedronate, and risedronate but was le
79 nsplantation, all patients received 90 mg of pamidronate i.v. every 12 weeks, regardless of pretransp
80 fety of continued treatment with intravenous pamidronate infusions for up to 2 years.
81                      Bisphosphonates such as pamidronate inhibit osteoclastic activity and reduce bon
82 trial was conducted using the bisphosphonate pamidronate intravenously in patients with new renal tra
83                                              Pamidronate is a useful adjunct to standard chemotherapy
84 riments indicate that the NH3(+)-terminus of pamidronate is close to the bone mineral surface, and a
85                                              Pamidronate is effective in reducing bony complications
86                                           IV pamidronate is recommended in women with pain caused by
87                                   Binding of pamidronate is well described by a Langmuir-like isother
88                                              Pamidronate is, therefore, a new lead compound for the s
89 nts overall, stratum 2 patients who received pamidronate lived longer than those who received placebo
90 studies suggest that bisphosphonates such as pamidronate may be efficacious.
91                                         This pamidronate-mediated augmentation of TNF-alpha productio
92 e an approximately 30-38 A2 surface area per pamidronate molecule and a deltaG = -4.3 kcal mol(-1).
93 ate therapy included zoledronate (n = 34) or pamidronate (n = 17) and pamidronate followed by zoledro
94                     Etidronate, alendronate, pamidronate, olpadronate, or amino-olpadronate (IG9402,
95                         TEDOR of [13C3, 15N] pamidronate on bone shows that the bisphosphonate binds
96 onate, were also compared with the action of pamidronate on proliferation of immortalized human fetal
97 hylamino)ethyl diphosphate, alendronate, and pamidronate on the pools of metabolites related to monot
98  therapy were randomized to receive 90 mg of pamidronate or placebo as a 2-hour intravenous infusion
99 randomly assigned to receive either 90 mg of pamidronate or placebo intravenously every 3 to 4 weeks
100 vations strongly suggest that treatment with pamidronate or zoledronate enhances the differentiation
101 reatment of PC3, DU145, and LNCaP cells with pamidronate or zoledronate significantly reduced the gro
102 studied 22 patients who received intravenous pamidronate or zoledronic acid for a duration of 3.6 yea
103 wever, the panel recommends only intravenous pamidronate or zoledronic acid in light of the use of th
104       Patients who received bisphosphonates (pamidronate or zoledronic acid) were identified.
105 no direct comparisons between clodronate and pamidronate or zoledronic acid, the superiority of one a
106  24 cycles in patients treated with 90 mg of pamidronate (P = .028, .023, and .008, respectively).
107 orubicin (Doxo) and coated with bone-seeking pamidronate (Pam) for the targeted treatment of malignan
108    Intravenous (IV) zoledronic acid (ZOL) or pamidronate (PAM) is recommended for preventing skeletal
109 ral mucosal tissue, we studied the effect of pamidronate (PAM), one of the BPs most commonly administ
110                                       In the pamidronate (Pam)-treated mice, but not control non-drug
111                                              Pamidronate preserved vertebral BMD during treatment and
112                                              Pamidronate prevents bone loss in the hip and lumbar spi
113                         Monthly infusions of pamidronate provide significant protection against skele
114            Treatment with the bisphosphonate pamidronate reduces skeletal complications and may also
115                                  The cost of pamidronate reflected the average wholesale price of the
116 n vivo (potency: risedronate > alendronate > pamidronate) requires expression of the Vgamma2Vdelta2 T
117 mplication was longer for patients receiving pamidronate than for those given placebo (P = .049).
118  complication was significantly less for the pamidronate than the placebo group at 15, 18, 21, and 24
119 alcemia were also statistically less for the pamidronate than the placebo group.
120                                           In pamidronate, the motion is well simulated by a gauche+/g
121  similar dosing guidelines are available for pamidronate, the Update Committee recommends that clinic
122             The temporal association between pamidronate therapy and the development of renal insuffi
123                                  The cost of pamidronate therapy exceeded the cost savings from preve
124 hough survival was not different between the pamidronate-treated group and placebo patients overall,
125 skeletal complication was 13.9 months in the pamidronate-treated women and 7.0 months in the placebo
126                        Using flow cytometry, pamidronate treatment (100 microM) was shown to induce s
127                                 In addition, pamidronate treatment increased total cellular protein,
128                            We also show that pamidronate treatment increases TNF-alpha production in
129                                              Pamidronate treatment was associated with development of
130  6 to 12, the subjects were observed without pamidronate treatment.
131 e effects in vivo of the bisphosphonate drug pamidronate, used in bone resorption therapy, were inves
132 -hoc evaluation of the cost-effectiveness of pamidronate using the results of two randomized trials t
133                             We conclude that pamidronate was more effective than control in improving
134 on in mice (giving a 60% survival rate), but pamidronate was not effective.
135                                              Pamidronate was safe and well tolerated during the 21 cy
136                                              Pamidronate was tolerated well.
137                                              Pamidronate was well tolerated.
138                                              Pamidronate was well tolerated.
139 rseded by second-generation bisphosphonates (pamidronate), which are more potent and do not have adve
140                                              Pamidronate, which is a member of the class of bisphosph
141            Treatment subjects (PAM) received pamidronate with vitamin D and calcium at baseline and a
142 15 minutes), versus the less expensive drug, pamidronate, with its longer infusion time (2 hours).
143 dental extraction (P = .009), treatment with pamidronate/zoledronate (P = .009), longer follow-up tim

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