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1 with effusion (COME) is the leading cause of conductive hearing loss.
2 loss in addition to the previously described conductive hearing loss.
3 excessive mucus contributes significantly to conductive hearing loss.
4 al disability), and ear anomalies, including conductive hearing loss.
5 e symptoms, including facial deformities and conductive hearing loss.
6 eletal defects and synostoses, which include conductive hearing loss.
7 e of the auditory brainstem during and after conductive hearing loss.
8 od bacterial infection, and leading cause of conductive hearing loss.
9 of the stapedial footplate and an associated conductive hearing loss.
14 n with chronic OM or recurrent OM often have conductive hearing loss and communication difficulties a
15 tis media with effusion (OME) often leads to conductive hearing loss and is a common feature of a num
16 second most prevalent form of hearing loss, conductive hearing loss and its effects on central synap
18 ions in joint range of motion, low-frequency conductive hearing loss, and functional oral deficits.
21 as performed and revealed moderate to severe conductive hearing loss bilaterally, with a mixed compon
22 rmed otosclerosis; the remaining nine have a conductive hearing loss but have not undergone correctiv
24 ere we induce a brief, reversible unilateral conductive hearing loss (CHL) at several experimentally
26 ore, we explored the effect of developmental conductive hearing loss (CHL) in gerbils on MMR characte
30 ow in young adult rats that 10 d of monaural conductive hearing loss (i.e., earplugging) leads to hea
32 h diseases, has been shown to directly cause conductive hearing loss in COME and airway obstruction i
35 Two forms of hearing loss were examined: conductive hearing loss in which the cochleae are not da
36 head and ears, and to compensate for natural conductive hearing losses, including those associated wi
40 findings suggest that (1) a broader range of conductive hearing-loss phenotypes are associated with N
42 heterozygotes show renal abnormalities and a conductive hearing loss similar to BOR syndrome, whereas
43 (3) NOG alterations should be considered in conductive hearing loss with subtle clinical and skeleta
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