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1 vident in patients with astrocytoma or mixed oligoastrocytoma.
2 plastic astrocytoma (AA) or anaplastic mixed oligoastrocytoma.
3 spinal cord neoplasms resembling human mixed oligoastrocytoma.
4 These GFAP/hPDGFB mice also developed spinal oligoastrocytoma.
5 cytomas, 64 oligodendrogliomas, and 16 mixed oligoastrocytomas.
6 2) of oligodendrogliomas and 67% (6 of 9) of oligoastrocytomas.
7 godendrogliomas (25 with 1p/19q loss) and 53 oligoastrocytomas (18 with 1p/19q loss) were investigate
9 ncluding oligodendroglioma, astrocytoma, and oligoastrocytoma, all of different histologic grades and
10 oglioma, astrocytoma, pilocytic astrocytoma, oligoastrocytoma, anaplastic astrocytoma, anaplastic oli
11 ndings in an immunocompetent patient with an oligoastrocytoma and the concomitant presence of the hum
12 h recurrent anaplastic oligodendrogliomas or oligoastrocytomas and recurrent low-grade gliomas had th
15 grade oligodendroglial neoplasms [anaplastic oligoastrocytoma (AOA) and anaplastic oligodendroglioma
16 ndrogliomas, pure (AO) and mixed (anaplastic oligoastrocytoma [AOA]), are chemosensitive, especially
17 cytomas, 52 oligodendrogliomas, and 31 mixed oligoastrocytomas), collected as part of an ongoing pros
18 luding astrocytomas, oligodendrogliomas, and oligoastrocytomas, formed a third cluster with a discret
19 ow-grade astrocytoma, oligodendroglioma, and oligoastrocytoma found somewhat lower survival and sligh
21 T2-weighted MR images, oligodendroglioma or oligoastrocytoma histopathologic type, and large tumor v
22 mation of either oligodendrogliomas or mixed oligoastrocytomas in about 40% of mice in the same time
23 of 1p and 19q loss in oligodendrogliomas and oligoastrocytomas in archival routinely processed paraff
24 s with low-grade oligodendroglioma (LGO) and oligoastrocytoma (LGOA), the majority will succumb to pr
25 included patients with grade 2 astrocytoma, oligoastrocytoma, or oligodendroglioma who were younger
26 ow-grade (WHO grade II) glioma (astrocytoma, oligoastrocytoma, or oligodendroglioma) with at least on
27 ow-grade (WHO grade II) glioma (astrocytoma, oligoastrocytoma, or oligodendroglioma) with at least on
28 mice developed oligodendrogliomas and mixed oligoastrocytoma tumors, instead of the fibrillary astro
29 grade oligodendrogliomas and low-grade mixed oligoastrocytomas) were examined with dynamic susceptibi
31 e I or II astrocytoma, oligodendroglioma, or oligoastrocytoma with clinically and radiologically stab
32 in 32% of patients and oligodendroglioma (or oligoastrocytoma with oligodendroglioma dominant) in 68%
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