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1 or coexisting Bosniak IV lesion and/or solid renal neoplasm.
2 sease gene associated with this rare form of renal neoplasm.
3 otype, 24 (45%) had at least one member with renal neoplasms.
4 ed as a fusion gene in a subset of pediatric renal neoplasms.
5 .1;q13), characteristic of another subset of renal neoplasms.
6 70 for nontransplanted control patients with renal neoplasms.
10 is kept in mind, if conditions that mimic a renal neoplasm are considered and excluded, and if there
11 s differentiation of high-density cysts from renal neoplasms by demonstrating deenhancement as a proo
13 who had a marking coil placed at biopsy of a renal neoplasm (coil group) and 23 patients who did not
15 eal of information regarding the genetics of renal neoplasms has also emerged from the extensive cyto
16 trategies in the evaluation and treatment of renal neoplasms have been fostered by developments in th
17 rcinoma (RCC) represents 10% to 15% of adult renal neoplasms; however, the molecular genetic events t
19 utopsy-based study was performed to evaluate renal neoplasms occurring in patients who underwent soli
22 wo cases of a hitherto undescribed pediatric renal neoplasm that is distinctive at the morphological,
23 umor cells and the identification of primary renal neoplasms that are genetically related to alveolar
25 th diethylstilbestrol- and estradiol-induced renal neoplasms, were observed in chromosomes 1, 2, 3, (
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