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Pediatric Dermatology|April 24, 2008
Dystrophic epidermolysis bullosa with one dominant and one recessive mutation of the COL7A1 gene in a child with deafnessSarah Weinel, Anne W Lucky, Jouni Uitto, et al.Developmental Biology|December 6, 2005
Molecular mechanisms underlying inner ear patterning defects in kreisler mutantsDaniel Choo, Jaye Ward, Alisa Reece, et al.Archives of Otolaryngology--Head & Neck Surgery|July 20, 2007
Functional magnetic resonance imaging of hearing-impaired children under sedation before cochlear implantationAnkur M Patel, Lisa D Cahill, Jennifer Ret, et al.International Journal of Pediatric Otorhinolaryngology|August 3, 2005
Audiometric, clinical and educational outcomes in a pediatric symptomatic congenital cytomegalovirus (CMV) population with sensorineural hearing lossColm Madden, Susan Wiley, Mark Schleiss, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|March 26, 2014
Functional communication of children who are deaf or hard-of-hearingJareen Meinzen-Derr, Susan Wiley, Sandra Grether, et al.Journal of the Association for Research in Otolaryngology : JARO|August 29, 2003
Expression of aquaporin 1 and 5 in the developing mouse inner ear and audiovestibular assessment of an Aqp5 null mutantMichele Merves, Carissa M Krane, Hongwei Dou, et al.BMJ Open|November 24, 2025
Standard medical care versus enhanced interdisciplinary care for implementation of positive airway pressure in youth with Down syndrome: a randomised controlled trial protocolMelissa S Xanthopoulos, Kelly Byars, Jareen Meinzen-Derr, et al.Journal of the American Academy of Audiology|February 27, 2025
Genetic and Clinical Predictors of Hearing Loss Among Patients with CHARGE SyndromeMaggie Kettler, Brittany Simpson, Jareen Meinzen-Derr, et al.Journal of Neurosurgery|March 24, 2004
Endolymphatic sac tumors in von Hippel-Lindau diseaseDaniel Choo, Lawrence Shotland, Maryann Mastroianni, et al.European Journal of Medical Genetics|November 15, 2020
CHARGE syndrome in the era of molecular diagnosis: Similar outcomes in those without coloboma or choanal atresiaBrittany N Simpson, Divya Khattar, Howard Saal, et al.Pageof 4