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1 igh rates of post-operative hearing loss and vestibular dysfunction.
2 mproves hearing sensitivity, and ameliorates vestibular dysfunction.
3 f hearing and vision, and varying degrees of vestibular dysfunction.
4 l defects and eventually to hearing loss and vestibular dysfunction.
5 ls only in the genetic background exhibiting vestibular dysfunction.
6 ilure of normal canal development results in vestibular dysfunction.
7 mic, hereditary hearing loss with associated vestibular dysfunction.
8 None of the strains displays signs of vestibular dysfunction.
9 ir death leads to permanent hearing loss and vestibular dysfunction.
10 that are useful models of human deafness and vestibular dysfunction.
11 ngenital deafness, retinitis pigmentosa, and vestibular dysfunction.
12 d for designing therapies to treat inner ear vestibular dysfunction.
13 of either central neurological or peripheral vestibular dysfunction.
14 target of mutations that cause deafness and vestibular dysfunction.
15 curring in DFNA9 leading to hearing loss and vestibular dysfunction.
16 t may cause or contribute to deafness and/or vestibular dysfunction.
17 itterbug (jbg), exhibit impaired hearing and vestibular dysfunction.
18 amed hurry-scurry (hscy) causes deafness and vestibular dysfunction.
19 tial for using antisense technology to treat vestibular dysfunction.
20 ) mouse carries a recessive mutation causing vestibular dysfunction.
21 re completely deaf and also display signs of vestibular dysfunction.
22 ated in ames waltzer and causes deafness and vestibular dysfunction.
23 causes hair cell degeneration, deafness, and vestibular dysfunction.
24 he inner ear that result in hearing loss and vestibular dysfunction.
25 het) is a recessive mutation in mice causing vestibular dysfunction.
26 ngenital deafness, retinitis pigmentosa, and vestibular dysfunction.
27 ion and navigational deficits observed after vestibular dysfunction.
28 ia was one indicating compensated peripheral vestibular dysfunction.
29 loss of vestibular hair cells and permanent vestibular dysfunction.
30 sociated with profound retinal, auditory and vestibular dysfunction.
31 tivity, Gpr156 mutant mice do not show overt vestibular dysfunction.
32 se likely contributes to the pathogenesis of vestibular dysfunction.
33 JLNS2), resulting in congenital deafness and vestibular dysfunction.
34 o treat synaptopathies linked to auditory or vestibular dysfunction.
35 Non-autonomic neurological causes included vestibular dysfunction (32 [5%]) and epilepsy (11 [1.7%]
36 low dose of DT caused profound SNHL without vestibular dysfunction and had no effect on wild-type (W
37 cargo whirlin are implicated in deafness and vestibular dysfunction and have been shown to localize a
39 congenital sensorineural deafness, constant vestibular dysfunction and prepubertal onset of retiniti
40 th Bt2 significantly reduced the severity of vestibular dysfunction and prevented earlier mortality.
42 disorder manifested by congenital deafness, vestibular dysfunction, and progressive retinal degenera
49 t prove useful in ameliorating some forms of vestibular dysfunction by modifying ongoing primary vest
50 ty-related symptoms; and (3) the severity of vestibular dysfunction can predict whether hyperactivity
51 has been eliminated in supporting cells have vestibular dysfunction caused by failure of synapse form
53 al, Tmc1(Delta)Tmc2(Delta) mice had profound vestibular dysfunction, deafness, and structurally norma
56 the severity rather than the age of onset of vestibular dysfunction differentiates whether hyperactiv
57 the waltzer (v) locus result in deafness and vestibular dysfunction due to degeneration of the neuroe
58 ouette (pi) locus result in hearing loss and vestibular dysfunction due to neuroepithelial defects in
59 inner (sr) locus results in hearing loss and vestibular dysfunction due to neuroepithelial defects in
61 etric effectively distinguishes animals with vestibular dysfunction from those with normal vestibular
65 nel-like 1 (TMC1) cause hearing loss without vestibular dysfunction in both mice and humans, we inves
68 tal deafness in humans and both deafness and vestibular dysfunction in mice homozygous for the shaker
69 vision symptoms in patients, our findings of vestibular dysfunction in these Dfnb31 mutants raise the
71 dels are powerful for assessing auditory and vestibular dysfunction, in vitro human inner ear models
72 T conditions, while clarifying the impact of vestibular dysfunction, individual characteristics, vary
78 here are a gene dose-sensitive cause of the vestibular dysfunction observed in EphB-Efnb2 signaling-
80 reflex (VOR) responses demonstrated that the vestibular dysfunction of the Zpld1 mutant mice is cause
83 life cognitive-motor demands in people with vestibular dysfunction (PwVD), functional gait and falls
84 similar hair bundle defects may underlie the vestibular dysfunction reported in humans with mutations
86 ess associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to
90 d without agoraphobia and to discern whether vestibular dysfunction was associated with specific symp
92 2a2 mutations cause hyperactivity; (2) it is vestibular dysfunction, which frequently co-occurs with
93 ke-wave seizures, cerebellar gait ataxia and vestibular dysfunction, which limit traditional approach
94 ain cause of balance disorders is peripheral vestibular dysfunction, which may occur as a result of h