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1 re needed to identify genetic alterations in pilocytic and low-grade astrocytomas, which account for
2 nges that drive the initiation and growth of pilocytic and other low-grade astrocytomas beyond the as
3 work should focus on elucidating features of pilocytic astocytomas that will identify prospectively c
4                The most common histology was pilocytic astrocytoma (46.3%).
5                                     Juvenile pilocytic astrocytoma (JPA) is one of the most common br
6 endymal giant cell astrocytomas (n = 4) or a pilocytic astrocytoma (n = 1) were treated with oral rap
7                                          The pilocytic astrocytoma (PA) is the most common childhood
8                                              Pilocytic astrocytoma (PA) is the most common glial cell
9 ncing (WGS) analysis of three NF1-associated pilocytic astrocytoma (PA) tumors.
10      The initial study cohort consisted of 7 pilocytic astrocytoma (PA), 19 ependymoma (EPN), 5 gliob
11                       Thirty-five samples of pilocytic astrocytoma and 10 control samples of cerebell
12 on a 4-yr-old male with a diagnosis of acute pilocytic astrocytoma and global cerebral hypoxic ischem
13 nses were observed (one in thalamic juvenile pilocytic astrocytoma and one in optic pathway glioma) a
14 iffuse glioma showed molecular similarity to pilocytic astrocytoma and relatively favorable survival.
15 ic nerve gliomas and in human NF1-associated pilocytic astrocytoma tumors.
16 y, EBV was the most frequent HHV detected in pilocytic astrocytoma, but at very low levels.
17 rs including oligodendroglioma, astrocytoma, pilocytic astrocytoma, oligoastrocytoma, anaplastic astr
18  craniopharyngioma, ependymoma, and juvenile pilocytic astrocytoma.
19  considered responsible for tumorigenesis of pilocytic astrocytoma.
20  multiforme (GBM) to the indolent, low-grade pilocytic astrocytoma.
21                                              Pilocytic astrocytomas (PAs) are the most common glioma
22                                              Pilocytic astrocytomas (PAs) are WHO grade I brain tumor
23                                              Pilocytic astrocytomas (PAs), WHO malignancy grade I, ar
24                                              Pilocytic astrocytomas (PAs, WHO grade I) are the most c
25 or predisposition syndrome develop low-grade pilocytic astrocytomas at an increased frequency.
26                                              Pilocytic astrocytomas of the optic nerve (optic nerve g
27                   These data illustrate that pilocytic astrocytomas overexpress specific NF1 gene tra
28                                              Pilocytic astrocytomas showed a marked predominance of t
29 5 astrocytic tumors including 21 GBMs and 19 pilocytic astrocytomas using oligonucleotide-based micro
30                      Low-grade brain tumors (pilocytic astrocytomas) arising in the neurofibromatosis
31 increased risk of brain tumors (particularly pilocytic astrocytomas) independently of gestational age
32                                There were 37 pilocytic astrocytomas, 34 medulloblastomas (23 classic,
33 e discrete cluster of gliomas identified the pilocytic astrocytomas, a second grouped the 1p/19q code
34  of seven oligodendrogliomas, three of three pilocytic astrocytomas, and one of five glioblastoma mul
35  NF1 gene acts as a tumor suppressor gene in pilocytic astrocytomas, and that NF1 gene expression wou
36 n with high fetal growth appeared to involve pilocytic astrocytomas, but not other astrocytomas, medu
37 presents tumors with molecular similarity to pilocytic astrocytomas, class II tumors are similar to 1
38 ole of the NF1 gene as a tumor suppressor in pilocytic astrocytomas, however, remains to be proven.
39 tween the ADC metrics and cellularity of the pilocytic astrocytomas, medulloblastomas, and ependymoma
40                                              Pilocytic astrocytomas, which contain abnormal glial cel
41 its central importance to the development of pilocytic astrocytomas.
42 s system tumors, including neurofibromas and pilocytic astrocytomas.
43 ignature that distinguished between GBMs and pilocytic astrocytomas.
44 pects of NF1 gene expression in six sporadic pilocytic astrocytomas.
45 e region on chromosome 17q occur in sporadic pilocytic astrocytomas.
46 viously, TDP-43 was detected in RFs of human pilocytic astrocytomas; however, involvement of TDP-43 i
47 sk of neurofibromas, schwannomas, low grade, pilocytic optic pathway gliomas, as well as malignant pe
48 ed human astrocytic tumors, but not sporadic pilocytic or other low-grade astrocytomas, specifically
49                          Histology (juvenile pilocytic v astrocytoma not otherwise specified [NOS]) w

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