Diagnosis, intervention, and prevention of genetic hearing loss

T Yang, L Guo, L Wang, X Yu - Hearing Loss: Mechanisms, Prevention …, 2019 - Springer
It is estimated that at least 50% of congenital or childhood hearing loss is attributable to
genetic causes. In non-syndromic hearing loss, which accounts for 70% of genetic hearing …

Importance of SLC26 transmembrane anion exchangers in sperm post-testicular maturation and fertilization potential

A Touré - Frontiers in Cell and Developmental Biology, 2019 - frontiersin.org
In mammals, sperm cells produced within the testis are structurally differentiated but remain
immotile and are unable to fertilize the oocyte unless they undergo a series of maturation …

[HTML][HTML] Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

MA Kim, SH Kim, N Ryu, JH Ma, YR Kim, J Jung… - Theranostics, 2019 - ncbi.nlm.nih.gov
Abstract Rationale: Mutations of SLC26A4 that abrogate pendrin, expressed in
endolymphatic sac, cochlea and vestibule, are known to cause autosomal recessive …

[PDF][PDF] Review of the Realation between Benign Paroxysmal Positional Vertigo and Vitamin D Deficiency

H Zarrinkoob, F Khateri… - The Scientific Journal of …, 2019 - scholar.archive.org
Abstract Background and Aims: Benign Paroxysmal Positional Vertigo (BPPV) is a common
cause of disabling vertigo with a high rate of occurrence. Today it is accepted that it is …

[引用][C] SLC26A4 基因突变致前庭水管扩大听力损失机制的研究进展

薛文悦, 陈正侬 - 中华耳科学杂志, 2019

مروری بر تاثیر ویتامین D بر سرگیجه خوش‌خیم وضعیتی

زرین کوب, خاطری, شعبانی, مسلم - دوماهنامه علمی-پژوهشی طب …, 2019‎ - medrehab.sbmu.ac.ir
مقدمه واهداف سرگیجه خوشخیم وضعیتی، شایعترین علت بروز سرگیجه با شیوع بالا میباشد.
امروزه این نوع سرگیجه در اثر جدا شدن ذرات اتوکنیا از ماکول اتریکول و شناور شدن این ذرات در …