نتایج جستجو برای: sensorineural deafness
تعداد نتایج: 31748 فیلتر نتایج به سال:
Abstract Background: Sensorineural hearing loss is one of the most common defects and half the cases are related to genetic factors. Given the importance of GJB2 mutations in hearing loss, this study was performed to study the impact of this mutation on hearing loss in selected families suffering from deafness. Materials and Methods: A descriptive study was performed on 8 GJB2 heterozygous ...
b-subunit crucial for renal Cl reabsorption and inner ear Kþ secretion. Nature 2001; 414: 558–561 3. Jeck N, Reinalter SC, Henne T et al. Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness. Pediatrics 2001; 108: E5 4. Shalev H, Ohali M, Kachko L, Landau D. The neonatal variant of Bartter syndrome and deafness: preservation of renal function. Pediatrics 200...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید