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1 d cancer that was refractory to radioiodine (iodine-131).
3 estimate the maximum tolerated dose (MTD) of iodine 131 ((131)I)-tositumomab (anti-CD20 antibody) tha
5 prednisone (CVP) followed by tositumomab and iodine-131 ((131)I) -tositumomab therapy were evaluated
7 ents exposed to radioactive iodines, chiefly iodine-131 ((131)I), after the 1986 Chornobyl (Ukrainian
8 ast one measurement of occult/minimal tumor (iodine 131[(131)I]-3F8 imaging, marrow immunocytology, o
9 of antibody labeled with escalating doses of iodine 131 (131I) was administered to patients with adva
10 proximately 740,000 Ci (2.73 x 10(16) Bq) of iodine 131 (131I) were released to the atmosphere from t
11 hnetium 99m (99mTc)-,iodine 123 (123I)-, and iodine 131 (131I)-labeled anti-CEA antibodies (all direc
12 ion tomography (PET), iodine-123- (123I) and iodine-131 (131I) -metaiodobenzylguanidine (MIBG), 111In
14 sure to low or moderate doses of radioactive iodine-131 (131I) at a young age is a public health conc
15 0 monoclonal antibody (anti-B1) labeled with iodine-131 (131I) in 34 patients with B-cell lymphoma wh
16 trahematopoietic toxicity was conducted with iodine-131 (131I) labeled monoclonal antibody (MAb) CC49
17 by a single dose of the therapeutic isotope iodine-131 (131I) without evidence of recurrence up to 5
19 patients treated with myeloablative doses of iodine-131-anti-CD20 antibody (anti-B1) and autologous s
20 ease, thyroid eye disease and treatment with iodine-131, antithyroid drug treatment, treatment of hyp
24 ancer not amenable to surgery or radioactive iodine ((131)I) therapy have few satisfactory therapeuti
27 py-relapsed/refractory patients treated with iodine (131)I tositumomab in a phase I/II single-center
33 okinetics, and dosimetry of intraventricular iodine-131-labeled monoclonal antibody 3F8 (131I-3F8) ta
34 aging evaluation that included iodine-123 or iodine-131 metaiodobenzylguanidine (MIBG) scan, bone sca
38 2 to 4 months included computed tomography, iodine-131-metaiodobenzylguanidine (131)I-MIBG; through
39 prior therapy on response and toxicity after iodine-131-metaiodobenzylguanidine (131I-MIBG) treatment
40 odine-124 PET study indicated that a dose of iodine-131 of 2000 cGy or more could be delivered to the
43 a, attributable to the very large amounts of iodine 131 released, was first noticed in children with
48 psed DLBCL were randomly assigned to receive iodine-131 tositumomab (dosimetric dose of 5 mCi on day
49 HL were treated in a phase I trial combining iodine-131 tositumomab (ranging from 0.30 to 0.75 Gy tot
51 t resulted in the regulatory approval of the iodine-131 tositumomab by the US Food and Drug Administr
52 ficacy, dosimetry methodology, and safety of iodine-131 tositumomab in patients with chemotherapy-rel
53 the five clinical trials of tositumomab and iodine-131 tositumomab in patients with relapsed or refr
56 ded toxicities apparent with the addition of iodine-131 tositumomab up to a dose of 0.75 Gy TBD to hi
62 essive thyroid cancer that was refractory to iodine-131, we randomly assigned 261 patients to receive
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