DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8
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The aim of the present study was to evaluate the potential morphologic risk factors for postoperative neurosensory… Expand BACKGROUND: Many preterm children display school difficulties, which may be mediated by impairment in executive function and… Expand PURPOSE
To elucidate the relationship between the anatomic position of the inferior alveolar nerve (IAN) at the mandibular second… Expand Congenital hearing loss occurs in approximately 1 in 1000 live births and 60% of these cases are hereditary.1,2 Non-syndromic… Expand PURPOSE
This study evaluated the location of the mandibular canal in the ramus of the mandible before bilateral sagittal split… Expand Approximately 50% of childhood deafness is caused by mutations in specific genes. Autosomal recessive loci account for… Expand Abstract. Two loci for nonsyndromic recessive deafness located on chromosome 21q22.3 have previously been reported, DFNB8 and… Expand Editor—Congenital deafness occurs in approximately 1 in 1000 live births and 50% of these cases are hereditary. Non-syndromic… Expand This retrospective study evaluated neurosensory dysfunction and the implant success rate associated with 64 implants placed in 15… Expand PURPOSE
This article addresses the suitability of semirigid fixation for the treatment of mandibular fractures.
MATERIALS AND… Expand