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1 of this protection results in cell death and sensorineural hearing loss.
2 Hair cell loss is a major cause of sensorineural hearing loss.
3 obodontia) segregating with a high-frequency sensorineural hearing loss.
4 own as a major target antigen for autoimmune sensorineural hearing loss.
5 lar disease associated with a high-frequency sensorineural hearing loss.
6 g mental retardation, vision impairment, and sensorineural hearing loss.
7 auses is irreversible and leads to permanent sensorineural hearing loss.
8 mited due to serious side effects, including sensorineural hearing loss.
9 ice hear well initially but show progressive sensorineural hearing loss.
10 ent and prognosis for patients with profound sensorineural hearing loss.
11 trated to improve outcomes for patients with sensorineural hearing loss.
12 l dominant form of progressive non-syndromic sensorineural hearing loss.
13 mice had a hyperactive circling behavior and sensorineural hearing loss.
14 pigmentary retinopathy and/or cataracts, and sensorineural hearing loss.
15 (p.Trp24*), which is an established cause of sensorineural hearing loss.
16 mentary retinopathy, cataracts, or both; and sensorineural hearing loss.
17 e witnessed a revolution in the treatment of sensorineural hearing loss.
18 ous parents and had an early onset bilateral sensorineural hearing loss.
19 significant cause of morbidity, particularly sensorineural hearing loss.
20 DFNBL, for autosomal recessive non-syndromic sensorineural hearing loss.
21 ed by progressive pigmentary retinopathy and sensorineural hearing loss.
22 circuits, and its mutation may contribute to sensorineural hearing loss.
23 ontine angle, and it typically presents with sensorineural hearing loss.
24 siblings had poor balance and 1 sibling had sensorineural hearing loss.
25 with a broad clinical spectrum that includes sensorineural hearing loss.
26 ble in the adult mammalian ear, resulting in sensorineural hearing loss.
27 s a rare disease that results in progressive sensorineural hearing loss.
28 ipheral facial paralysis and 2 patients with sensorineural hearing loss.
29 anguineous family with moderate nonsyndromic sensorineural hearing loss.
30 ory-filter characteristics of listeners with sensorineural hearing loss.
31 ogenitors and mutations in these genes cause sensorineural hearing loss.
32 of the inner ear, which ultimately leads to sensorineural hearing loss.
33 ng GJB2 gene lead to many skin disorders and sensorineural hearing loss.
34 recurring episodes of sudden or progressive sensorineural hearing loss.
35 lit-foot type 1 malformation associated with sensorineural hearing loss.
36 rder characterized by ovarian dysgenesis and sensorineural hearing loss.
37 ardiomyopathy, kidney and liver disease, and sensorineural hearing loss.
38 articipants were 36 adults with symmetrical, sensorineural hearing loss (18 experienced hearing instr
39 sequential probands referred for congenital sensorineural hearing loss, 22 (42%) were found to have
40 tic (venous thrombosis 25%, lymphedema 11%), sensorineural hearing loss 76%, miscarriage 33%, and hyp
42 fy mutations in Gipc3 underlying progressive sensorineural hearing loss (age-related hearing loss 5,
44 otogl with morpholinos in zebrafish leads to sensorineural hearing loss and anatomical changes in the
46 292 had no polyneuropathy or ataxia, and the sensorineural hearing loss and cataract were attributed
47 a good animal model to evaluate the role of sensorineural hearing loss and central inhibition in aud
48 ion in multiple tissues, suggesting that the sensorineural hearing loss and characteristic brain malf
49 ilitate early detection and intervention for sensorineural hearing loss and developmental delay, wher
51 developmental abnormalities of the cochlea, sensorineural hearing loss and diffuse thyroid enlargeme
52 dered in patients presenting with congenital sensorineural hearing loss and disorders of cornificatio
55 erturn a long-standing dogma in the study of sensorineural hearing loss and highlight the importance
56 ty of hearing-loss disorders, such as sudden sensorineural hearing loss and Meniere's disease that ar
58 autosomal recessive disorder associated with sensorineural hearing loss and pili torti, is caused by
59 d that an absence of Np65 causes early-onset sensorineural hearing loss and prevented the normal syna
60 ant mice, absence of Np65 causes early-onset sensorineural hearing loss and prevents normal neurotran
61 disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pig
62 disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pig
63 racterized by progressive pontobulbar palsy, sensorineural hearing loss and respiratory insufficiency
64 der characterized by the association between sensorineural hearing loss and thyroid swelling or goitr
65 ) gene, causing the adult-onset, progressive sensorineural hearing loss and vestibular disorder at th
66 e etiologic for the late-onset, progressive, sensorineural hearing loss and vestibular dysfunction kn
67 a syndrome consisting of encephalomyopathy, sensorineural hearing loss, and hypertrophic cardiomyopa
68 who presented with osteoporosis, cataracts, sensorineural hearing loss, and mild learning defects.
69 s much to learn about pathogenesis of sudden sensorineural hearing loss, and more clinical trials are
70 wo thirds of respondents were male, most had sensorineural hearing loss, and most were older than 50;
71 al-recessive inheritance, severe to profound sensorineural hearing loss, and partial agenesis of the
72 nction, cachetic dwarfism, photosensitivity, sensorineural hearing loss, and retinal degradation.
73 llar ataxia, early-onset cerebellar atrophy, sensorineural hearing loss, and the distinctive associat
74 etely penetrant, predominantly low-frequency sensorineural hearing loss, and the Fgfr3(P244R) mice sh
76 members inherited pili torti and prelingual sensorineural hearing loss as autosomal recessive traits
81 spontaneous attacks of vertigo, fluctuating sensorineural hearing loss, aural fullness, and tinnitus
82 d-responsive, rapidly progressive, bilateral sensorineural hearing loss (autoimmune inner ear disease
83 obtained from 49 participants with moderate sensorineural hearing loss before fitting and after 3 we
84 cause of neurological problems, particularly sensorineural hearing loss, but data on long-term sequel
85 vide significant benefit for a wide range of sensorineural hearing loss, but no carefully controlled,
86 gs to more clinically relevant conditions of sensorineural hearing loss by examining the role of frac
87 that this variant may modify the severity of sensorineural hearing loss caused by a variety of factor
89 cterized by pigmentary retinal degeneration, sensorineural hearing loss, childhood obesity, non-insul
91 Patients with ATP6B1 mutations also have sensorineural hearing loss; consistent with this finding
92 disability, hypotonia, spasticity, seizures, sensorineural hearing loss, cortical visual impairment,
93 oximately 20-30% of patients with congenital sensorineural hearing loss demonstrate radiographic abno
94 plantation, the current therapy for profound sensorineural hearing loss, depends on a functional nerv
95 ocus responsible for postlingual progressive sensorineural hearing loss (designated DFNA9) that maps
96 nalysis of dominantly inherited, progressive sensorineural hearing loss DFNA41 in a six-generation ki
98 rophy, neuropathy, myopathy, cardiomyopathy, sensorineural hearing loss, diabetes mellitus, and other
99 oding connexin 26 (cx26) have been linked to sensorineural hearing loss either alone or as part of a
100 results in vertebral compression fractures, sensorineural hearing loss, eye defects, and heart defec
101 bers show a bilateral, sloping, progressive, sensorineural hearing loss, first evident at 6000 and 80
102 elin plasticity and how this could relate to sensorineural hearing loss following peripheral impairme
107 either common (hearing loss) or distinctive (sensorineural hearing loss in a child), they are importa
108 t, progressive, high-frequency, nonsyndromic sensorineural hearing loss in a large, multigenerational
109 te OPG at high levels and lack of OPG causes sensorineural hearing loss in addition to the previously
113 channel-like gene 1 (TMC1) cause progressive sensorineural hearing loss in humans and Beethoven (Tmc1
116 GED1 loss, and a diversity of conductive and sensorineural hearing loss in nearly half of AGS patient
117 53G > A), of NLRP3 causes autosomal-dominant sensorineural hearing loss in two unrelated families.
118 oss in which the cochleae are not damaged or sensorineural hearing loss in which both cochleae are re
119 cted in two unrelated persons with increased sensorineural hearing loss, in the other caused by a mut
120 coustic trauma, one of the leading causes of sensorineural hearing loss, induces sensory hair cell da
125 e not precipitated by cold exposure and that sensorineural hearing loss is frequently also present.
129 sible causes of hearing loss, such as sudden sensorineural hearing loss, is important to maximize the
131 sly unknown autosomal-recessive nonsyndromic sensorineural hearing loss locus (DFNB91) to chromosome
134 more likely than controls to have bilateral sensorineural hearing loss of 40 dB or more (unmatched 1
135 syndrome that includes the subacute onset of sensorineural hearing loss, often accompanied by vertigo
136 verlapping clinical features, manifesting as sensorineural hearing loss, often associated with vertig
137 racterized by mental retardation, hypotonia, sensorineural hearing loss, optic atrophy, and other fea
138 s a higher risk of adverse neonatal outcome (sensorineural hearing loss or neurological deficits).
139 otitis media (OM), including high-frequency sensorineural hearing loss or vertigo, is not uncommon.
140 autosomal dominant disorder characterized by sensorineural hearing loss, palmoplantar keratoderma, kn
141 regating an autosomal dominant, progressive, sensorineural hearing loss phenotype that has been linke
142 man with a history of progressive bilateral sensorineural hearing loss presented to a neuro-ophthalm
143 trial involving 250 patients with unilateral sensorineural hearing loss presenting within 14 days of
144 mbrane abnormalities may be one aetiology of sensorineural hearing loss primarily affecting the mid-f
145 iginally identified in Persian families with sensorineural hearing loss, regulates peroxisomal dynami
146 ic TBS patients by displaying high-frequency sensorineural hearing loss, renal cystic hypoplasia and
147 year-old female has intellectual disability, sensorineural hearing loss requiring bilateral cochlear
148 cochlea, caused by macular degeneration and sensorineural hearing loss, respectively, affect a growi
150 d whole-exome sequencing in individuals with sensorineural hearing loss (SNHL) and identified pathoge
152 Hippel-Lindau disease and cause irreversible sensorineural hearing loss (SNHL) and vestibulopathy.
156 Behavioral studies in humans suggest that sensorineural hearing loss (SNHL) decreases sensitivity
157 e to four decades, the incidence of acquired sensorineural hearing loss (SNHL) in children living in
159 Lassa virus (LASV)-infected patients develop sensorineural hearing loss (SNHL) in the late stages of
163 ngenital cytomegalovirus (CMV) infection and sensorineural hearing loss (SNHL) was first described al
165 s a rare recessive disorder characterized by sensorineural hearing loss (SNHL), amelogenesis imperfec
166 terized by vascularizing keratitis, profound sensorineural hearing loss (SNHL), and progressive eryth
171 -five percent of people with VS present with sensorineural hearing loss (SNHL); the mechanism of this
174 transcriptional co-activator EYA4 gene cause sensorineural hearing loss that can occur in association
175 2 represents a locus for congenital profound sensorineural hearing loss that has yet to be mapped.
176 describe 2 unrelated pedigrees with MTP and sensorineural hearing loss that segregate with a DIAPH1
177 anging from highly restricted pili torti and sensorineural hearing loss (the Bjornstad syndrome) to p
178 of hair cells or auditory neurons results in sensorineural hearing loss, the consequence of supportin
179 chronic disorder of the inner ear defined by sensorineural hearing loss, tinnitus and episodic vertig
180 ting from minutes to hours, with fluctuating sensorineural hearing loss, tinnitus, and aural pressure
181 siblings presented with autosomal recessive sensorineural hearing loss: two had high-frequency loss,
182 rized by fever, chronic meningitis, uveitis, sensorineural hearing loss, urticarial skin rash, and a
183 essive disorder characterized by progressive sensorineural hearing loss, vestibular dysfunction, and
189 utosomal dominant, nonsyndromic, progressive sensorineural hearing loss with vestibular pathology.
190 sease erythrokeratoderma variabilis (EKV) or sensorineural hearing loss with/without peripheral neuro
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