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Ns. Some of the participants mentioned reasons not listed in our questionnaire such as being ashamed to appear in public with a bandaged nose anda dislike for attracting attention. Some others mentioned that they believe whatever god has created is beautiful and should not be manipulated.Table 3: Attitude toward rhinoplastyHow do you feel about your nose? Happy Not Happy Don't care Do you want to
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Ns made in this study. That is, subjects were able to review their prior responses made preoperatively with acoustic stimulation alone when making their responses at the 6month evaluation. The APHAB was added in Phase 2 of the study, and were not administered to those implanted prior to Phase 2. The CD-recorded speech perception tests were administered in a calibrated sound-field at 70 dBC, with p
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Ial was initiated with optimally fitted amplification prior to baseline testing. Optimally fitted amplification characteristics were determined based on targets derived from the National Acoustics Laboratories (NAL) hearing aid fitting procedure17,18. Preoperatively, the CNC words and BKB-SIN tests were administered: 1. 2. 3. with acoustic stimulation provided in the ear to be implanted, with acou
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Electrode was designed to be minimally invasive and only enter the descending basal turn of the scala tympani between 190 and 200 degrees. This short intracochlear electrode had a reduced diameter of 0.2 X 0.4 mm as compared to standard-length cochlear implants. Six electrodes (channels) are located in the distal 5 mm of the electrode. The device was placed through a 0.5?.6 mm cochleostomy located
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S, etiology of the hearing loss was unknown (41/87 or 47.1 ), with many describing a family history of hearing loss (22/87 or 25.3 ). Etiologies of hearing loss in the remaining subjects included: history of noise exposure (15/87 or 17.2 ), autoimmune inner ear disease (2/87 or 2.3 ), measles (2/87 or 2.3 ), ototoxicity, neuritis, large vestibular aqueduct syndrome, Usher's Syndrome and endolympha
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AnuscriptGantz et al.PageS8 implant data was published in 200912 and this report describes the final outcome of the clinical trial.Author Manuscript Author Manuscript Author Manuscript Author ManuscriptMethodsParticipants Eighty-seven subjects in the U.S. received Nucleus?HybridTM S8 implants (with 6 contacts across 10 mm electrodes) under an Investigational Device Exemption (IDE). The subjects in
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