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1 4 to 0.949 +/- 0.027 g/cm(2), P < 0.001 with ibandronate).
2 nd the amino bisphosphonates alendronate and ibandronate.
3 decreased osteoblast numbers in response to ibandronate.
4 results, a relatively high concentration of ibandronate (100 microM) increased caspase-3 activity an
5 e efficacy, adherence, and safety of monthly ibandronate (150 mg) with weekly alendronate (70 mg) wer
7 dose-dense chemotherapy regimens and 2:1 to ibandronate 50 mg per day orally for 2 years or observat
10 in-of-function mutants are also resistant to ibandronate, an inhibitor of an enzyme downstream of HMG
14 reported odds ratios (RORs) for alendronate, ibandronate, and risedronate were 3.82 (95% CI: 2.94-4.9
15 for treatment of osteoporosis (alendronate, ibandronate, and risedronate) and treatment/prevention o
19 n increase in disease-free survival (DFS) by ibandronate from 75% to 79.5% by using a two-sided alpha
21 a combination therapy of low dose parenteral ibandronate (IBN) and calcitriol on top of calcium and v
22 oth regimens, weekly alendronate and monthly ibandronate, improve bone mass and are comparable in saf
23 ned the effects of the potent bisphosphonate ibandronate in a murine model of human myeloma bone dise
25 , z-Val-Ala-Asp-fluoromethyl ketone, blocked ibandronate-induced DNA fragmentation in MDA-231 cells,
31 e either been recently released (intravenous ibandronate), or have completed (zoledronic acid) or are
32 e either been recently released (intravenous ibandronate), or have completed (zoledronic acid) or are
35 istomorphometrical examination revealed that ibandronate reduced osteoclastic bone resorption, with i
37 dence suggests that alendronate, etidronate, ibandronate, risedronate, zoledronic acid, estrogen, par
41 treatment with the bisphosphonate compound, ibandronate, significantly delayed the progression of os
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