O'Reilly RC - Search Results

1

Cortical Auditory Evoked Potential Testing in Children With Auditory Neuropathy Spectrum Disorder.

Morlet T, Valania J, Walter C, Morini G, O'Reilly RC, Parkes W, Pritchett C. Morlet T, et al. Among authors: o reilly rc. Am J Audiol. 2023 Dec 4:1-12. doi: 10.1044/2023_AJA-23-00051. Online ahead of print. Am J Audiol. 2023. PMID: 38048283

2

A 15-year Review of 260 Children With Auditory Neuropathy Spectrum Disorder: II. Management and Outcomes.

Morlet T, O'Reilly R, Pritchett C, Venskytis E, Parkes W. Morlet T, et al. Ear Hear. 2023 Sep-Oct 01;44(5):979-989. doi: 10.1097/AUD.0000000000001366. Epub 2023 Apr 10. Ear Hear. 2023. PMID: 37036283

3

A 15-Year Review of 260 Children With Auditory Neuropathy Spectrum Disorder: I. Demographic and Diagnostic Characteristics.

Morlet T, Parkes W, Pritchett C, Venskytis E, DeVore B, O'Reilly RC. Morlet T, et al. Among authors: o reilly rc. Ear Hear. 2023 Sep-Oct 01;44(5):969-978. doi: 10.1097/AUD.0000000000001337. Epub 2023 Apr 10. Ear Hear. 2023. PMID: 37036288

4

Mutations in LOXHD1 gene can cause auditory neuropathy spectrum disorder.

Morlet T, Robbins KM, Stabley D, Holbrook J; University of Washington Center for Mendelian Genomics; Sol-Church K, O'Reilly RC. Morlet T, et al. Among authors: o reilly rc. Otolaryngol Case Rep. 2021 Nov;21:100367. doi: 10.1016/j.xocr.2021.100367. Epub 2021 Oct 9. Otolaryngol Case Rep. 2021. PMID: 35875410 Free PMC article.

5

Clinical characteristics of children with cochlear nerve dysplasias.

Levi J, Ames J, Bacik K, Drake C, Morlet T, O'Reilly RC. Levi J, et al. Laryngoscope. 2013 Mar;123(3):752-6. doi: 10.1002/lary.23636. Epub 2012 Oct 19. Laryngoscope. 2013. PMID: 23086614

6

Cochlear Nerve Deficiency and Brain Abnormalities in Pediatric Patients.

Morlet T, Pazuniak M, O'Reilly RC, Kandula V, Choudhary AK. Morlet T, et al. Otol Neurotol. 2017 Mar;38(3):429-440. doi: 10.1097/MAO.0000000000001308. Otol Neurotol. 2017. PMID: 28060175

7

Auditory nerve function following cochleitis.

Levi J, Looney L, Murray R, Inverso Y, O'Reilly RC, Morlet T. Levi J, et al. Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1696-701. doi: 10.1016/j.ijporl.2012.08.003. Epub 2012 Sep 17. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22995199

8

A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans.

Morlet T, Rabinowitz MR, Looney LR, Riegner T, Greenwood LA, Sherman EA, Achilly N, Zhu A, Yoo E, O'Reilly RC, Jinks RN, Puffenberger EG, Heaps A, Morton H, Strauss KA. Morlet T, et al. Laryngoscope. 2014 Mar;124(3):E95-103. doi: 10.1002/lary.24361. Epub 2013 Dec 17. Laryngoscope. 2014. PMID: 23946138 Free PMC article.

9

Central auditory processing deficiency with anatomic deficit in left superior temporal lobe.

Grindle CR, O'Reilly RC, Morlet T, Finden S. Grindle CR, et al. Laryngoscope. 2010 Aug;120(8):1671-4. doi: 10.1002/lary.20986. Laryngoscope. 2010. PMID: 20564663

10

Prevalence of vestibular and balance disorders in children.

O'Reilly RC, Morlet T, Nicholas BD, Josephson G, Horlbeck D, Lundy L, Mercado A. O'Reilly RC, et al. Otol Neurotol. 2010 Dec;31(9):1441-4. doi: 10.1097/MAO.0b013e3181f20673. Otol Neurotol. 2010. PMID: 20729773

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