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Feasibility of Self-Programming of the Speech Processor Via Remote Assistant Fitting in Experienced Cochlear Implant Users
Published 2025-01-01Subjects: Get full text
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Exogenous neuritin restores auditory following cochlear spiral ganglion neuron denervation of gerbils
Published 2024-03-01Subjects: Get full text
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A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families
Published 2018-01-01“…Our study showed that targeted NGS is an effective tool for diagnosis of genetic deafness and that p.G141R in ILDR1 may be a relatively frequent mutation for DFNB42 in Chinese Hans.…”
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            146
La médiation culturelle pour les sourds dans le milieu muséal au Québec
Published 2017-10-01Subjects: Get full text
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            147
Penggunaan bahasa isyarat dalam pembelajaran seni tari bagi siswa tunarungu tingkat sekolah menengah pertama di sekolah luar biasa
Published 2024-10-01Subjects: “…dance learning, deaf students, sign language…”
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            148
A qualitative research on perceptions and experience of patients with sudden deafness (突发性聋患者疾病感受和体验的质性研究)
Published 2023-05-01Subjects: “…sudden deafness…”
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            149
Bilateral Sensorineural Deafness in a Young Pregnant Female Presenting with a Fever: A Rare Complication of a Reemerging Disease—Spotted Fever Group Rickettsioses
Published 2019-01-01“…Sensorineural deafness is a rare complication of spotted fever group rickettsioses. …”
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Interaural level difference sensitivity in neonatally deafened rats fitted with bilateral cochlear implants
Published 2024-12-01Subjects: “…Deafness…”
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            151
Congenital rubella syndrome and its protean manifestation in Nigeria
Published 2024-11-01Subjects: Get full text
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            152
Case report: A novel nonsense mutation in the MARVELD2 gene causes nonsyndromic hearing loss in a China family
Published 2024-12-01Subjects: “…Deafness gene…”
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            153
De l’entorse à la norme à l’atypicité typique : Retour sur un corpus de SMS de sourds et ses métadonnées
Published 2019-04-01Subjects: Get full text
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KELALAIAN PPAT ATAS PERBUATAN MELAWAN HUKUM ANAK TIRI PEMBELI TERHADAP TUNA AKSARA
Published 2023-05-01Subjects: “…Deaf…”
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Komunikasi Nonverbal Guru pada Murid Tunarungu dalam Meningkatkan Kemampuan Berinteraksi Sosial
Published 2020-01-01Subjects: “…nonverbal communication, deaf people, extraordinary primary school.…”
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Genetic and audiological determinants of hearing loss in high-risk neonates
Published 2025-03-01Subjects: Get full text
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            157
The Egyptian Revolution: First Impressions from the Field
Published 2011-02-01Subjects: Get full text
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A novel therapeutic pathway to the human cochlear nerve
Published 2024-11-01Subjects: Get full text
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Evaluation of disparities in hospitalisation outcomes for deaf and hard of hearing patients with COVID-19: a multistate analysis of statewide inpatient databases from Florida, Maryland, New York and Washington
Published 2025-01-01“…Objective Investigate whether deaf or hard of hearing (D/HH) patients with COVID-19 exhibited different hospitalisation outcomes compared with hearing patients with COVID-19.Design Cohort studySetting Statewide Inpatient Databases for Florida, Maryland, New York and Washington, for the year 2020.Participants Records of patients aged 18–64 years with COVID-19Primary outcomes and measures Differences in in-hospital death, 90-day readmission, length of stay, hospitalisation cost, hospitalisation cost per day, intensive care unit (ICU) or coronary care unit (CCU) utilisation and ventilation use were evaluated. …”
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Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)
Published 2019-01-01“…The accuracy of in silico pathogenicity prediction tools has not been previously assessed for variants associated with autosomal recessive deafness 1A (DFNB1A). Here, we identify in silico tools with the most accurate clinical significance predictions for missense variants of the GJB2 (Cx26), GJB6 (Cx30), and GJB3 (Cx31) connexin genes associated with DFNB1A. …”
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