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1 crosurgical resection for acoustic neuromas (vestibular schwannomas).
2 rilymph (PL), cerebrospinal fluid (CSF), and vestibular schwannoma.
3 facial paralysis after surgical treatment of vestibular schwannoma.
4 veloped facial paralysis after treatment for vestibular schwannoma.
5 imary and diagnostic tumor type is bilateral vestibular schwannoma.
6 haracterized by the development of bilateral vestibular schwannomas.
7 nations were performed in nine patients with vestibular schwannomas.
8 th a reduction in the volume of most growing vestibular schwannomas.
9 t problem and the cardinal sign is bilateral vestibular schwannomas.
10 NF2m-IRF3 condensates were evident in human vestibular schwannomas.
11 haracterized by the development of bilateral vestibular schwannomas.
12 t, accurate AI for 3D volumetric analysis of vestibular schwannomas.
13 ary adenoma (1.21, 1.16-1.25, p<0.0001), and vestibular schwannoma (1.19, 1.04-1.35, p=0.0085), and i
14 ary adenoma (1.13, 1.05-1.22, p<0.0001), and vestibular schwannoma (1.48, 1.19-1.84, p<0.0001) when c
18 26 years) with progressive target tumors (10 vestibular schwannomas, 8 nonvestibular schwannomas, 20
20 ith a newly diagnosed (<6 months) unilateral vestibular schwannoma and a maximal tumor diameter of le
21 canals of patients with Meniere's disease or vestibular schwannoma and measured the endolymph-to-peri
22 ial schwannoma had an LZTR1 mutation (3 were vestibular schwannomas and 1 was a nonvestibular schwann
24 ors and the therapeutic targeting of PAK1 in vestibular schwannomas and argue against PAK1 and PAK2 e
25 e evaluations, particularly in patients with vestibular schwannomas and candidates for cochlear impla
26 redict the degree of tumor-brain adhesion of vestibular schwannomas and may provide a method to impro
28 dominant disease characterized by bilateral vestibular schwannomas and other nonmalignant tumors of
29 ion of vascular endothelial growth factor by vestibular schwannomas and the role of Notch signaling i
31 inform treatment decisions for patients with vestibular schwannoma, and further investigation of long
32 All 5 had multiple tumors in addition to vestibular schwannoma, and none had a positive family hi
35 ate normal anatomic structures, evaluate for vestibular schwannomas, assess for inflammatory and/or i
37 ilin-2, in paraffin-embedded samples from 21 vestibular schwannomas associated with neurofibromatosis
38 meningioma, glioblastoma, pituitary adenoma, vestibular schwannoma, astrocytoma, and oligodendrogliom
39 5% male) who underwent surgical resection of vestibular schwannoma at 66 reporting facilities, the me
40 c measures differed between individuals with vestibular schwannoma (at both time points) and healthy
41 movements were measured in individuals with vestibular schwannoma before and then 6 weeks after unil
42 genetic condition associated with bilateral vestibular schwannomas, benign tumors that arise from th
43 roughput miRNA expression profiling of human vestibular schwannomas by using an array representing 40
45 ssociation study in a cohort of 911 sporadic vestibular schwannoma cases collated from the neurofibro
46 lume, defined as the mean number of surgical vestibular schwannoma cases per year in the 2 years prec
47 a reduction in VOR gain for individuals with vestibular schwannoma compared to control subjects, that
48 phosphorylated forms were elevated in human vestibular schwannomas compared with normal human Schwan
49 tify novel genetic associations with risk of vestibular schwannoma development, we conducted a genome
51 enrolled at the Norwegian National Unit for Vestibular Schwannoma from October 28, 2014, through Oct
53 Patients with multiple schwannomas without vestibular schwannomas have been postulated to compose a
58 Patients with hearing loss (134 positive for vestibular schwannoma [mean age +/- SD, 54 years +/- 12;
59 w-grade tumors affecting the cranial nerves (vestibular schwannomas), meninges (meningiomas), and spi
60 47), pituitary adenoma (n=27 506; n=87 772), vestibular schwannoma (n=11 525; n=30 745), astrocytoma
62 tion syndrome that is manifested by multiple vestibular schwannomas, nonvestibular schwannomas, menin
63 aring loss (ARHL); (2) neuropathy related to vestibular schwannoma or neurofibromatosis of type 2; (3
64 imaging is the study of choice to exclude a vestibular schwannoma or other neoplasm of the cerebello
65 Neurofibromatosis 2 (NF2) features bilateral vestibular schwannomas, other benign neural tumors, and
66 association between hearing loss in sporadic vestibular schwannoma patients and the proteome of peril
68 icate chronic inflammation in the cochlea of vestibular schwannoma patients with severe to profound h
69 live, mature utricles from organ donors and vestibular schwannoma patients, and present a validated
71 idelines for treating small- to medium-sized vestibular schwannoma recommend either upfront radiosurg
75 ort study found that among adults undergoing vestibular schwannoma surgery, a higher facility case vo
78 cohort study found that, among patients with vestibular schwannoma, symptoms present at initial evalu
79 ive sampling of PL and of CSF, and biopsy of vestibular schwannoma tissue, was performed in 32, 32, a
81 rgery following failed primary SRS/FSRT in 7 vestibular schwannoma treatment centers across the US an
84 with newly diagnosed small- and medium-sized vestibular schwannoma, upfront radiosurgery demonstrated
85 ch are unexpectedly 14-fold more abundant in vestibular schwannoma utricles, demonstrating the existe
88 ts before resection of a sporadic unilateral vestibular schwannoma (VS) in order to assess function r
93 advanced age on surgical outcomes following vestibular schwannoma (VS) resection, few if any large-s
94 elf-reported occupational noise exposure and vestibular schwannoma (VS), found in several studies, re
98 pe 2 (NF2)-related schwannomas, 104 sporadic vestibular schwannomas (VS) and 38 schwannomatosis-relat
102 coordination impairments in individuals with vestibular schwannomas (VS) remains a challenge, particu
103 nherited disorder characterized by bilateral vestibular schwannomas (VS) that arise from neoplastic S
104 type 2 (NF2) is a rare disorder that causes vestibular schwannomas (VS), meningiomas and ependymomas
107 position syndrome characterized by bilateral vestibular schwannomas (VSs) resulting in deafness and b
111 head-on-trunk kinematics in individuals with vestibular schwannoma were actually comparable before an
112 ssic type 2 neurofibromatosis with bilateral vestibular schwannomas were analyzed for mutations in th
113 54 years +/- 12;64 men] and 80 negative for vestibular schwannoma) were randomly assigned to a train
114 heral nerve schwannomas, including bilateral vestibular schwannomas which are associated with substan
115 udy of adults (>=18 years old) with sporadic vestibular schwannoma who underwent salvage microsurgery
116 ith neurofibromatosis type 2 and progressive vestibular schwannomas who were not candidates for stand