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Mutations in the GJB2 gene are a major cause of non‐syndromic recessive hearing loss in many countries. In a significant fraction of patients, only monoallelic GJB2 mutations known to be either recessive or of unclear pathogenicity are... more
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Background:The Bluetooth wireless headset has been promoted as a ‘hands-free’ device with a low emission of electromagnetic radiation.Objective:To evaluate potential changes in hearing function as a consequence of using Bluetooth devices,... more
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      Cell PhonesHearingProspective studiesHumans
COVID 19 has restricted much face to face communication. Many Aboriginal people only have access to phones to participate in tele communication. However, phone communication is difficult for the many Aboriginal people who have hearing... more
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Precondition to prevention and control of morbidity and mortality of myocardial ischemia--coronary disease, is its good diagnostic. Goal of this study is to asses diagnostic significance of positive trademill stress test in diagnosis of... more
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Auditory distance perception plays a major role in spatial awareness, enabling location of objects and avoidance of obstacles in the environment. However, it remains under-researched relative to studies of the directional aspect of sound... more
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We report an unusual case of encephalo-entero-myopathy associated with the A8344G mutation in the tRNA(Lys) gene of mitochondrial DNA (mtDNA). This patient had mitochondrial myopathy, multiple lipomatosis, mild hearing loss, stroke-like... more
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Thresholds for a 6.5-kHz sinusoidal signal, temporally centered in a 400-ms broadband-noise masker, were measured as a function of signal duration for normally hearing listeners and listeners with cochlear hearing loss over a range of... more
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