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The American Journal of Otology|January 26, 1999
Cracking the auditory genetic code: nonsyndromic hereditary hearing impairmentA K Lalwani, C M CasteleinAmerican Journal of Human Genetics|October 12, 2000
Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9A K Lalwani, J A Goldstein, M J Kelley, et al.Otolaryngologic Clinics of North America|June 1, 1992
Meningiomas, epidermoids, and other nonacoustic tumors of the cerebellopontine angleA K LalwaniThe Laryngoscope|October 19, 2000
Sensorineural and conductive hearing loss associated with lateral semicircular canal malformationJ Johnson, A K LalwaniThe American Journal of Otology|January 26, 1999
The effect of cochleostomy and intracochlear infusion on auditory brain stem response threshold in the guinea pigG J Carvalho, A K LalwaniInternational Journal of Pediatric Otorhinolaryngology|November 1, 1992
Teratoma of the tongue: a case report and review of the literatureA K Lalwani, T L EngelThe American Journal of Otology|November 1, 1991
Spontaneous hemotympanum associated with chronic middle ear effusionA K Lalwani, R K JacklerOtolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|July 1, 1993
Preoperative differentiation between meningioma of the cerebellopontine angle and acoustic neuroma using MRIA K Lalwani, R K JacklerInternational Journal of Pediatric Otorhinolaryngology|November 30, 1999
Cochlear gene therapy: current perspectivesM J Wareing, A K LalwaniInternational Journal of Pediatric Otorhinolaryngology|January 4, 2001
Inner ear malformations and hearing loss in linear nevus sebaceous syndromeK C Yu, A K LalwaniPageof 9