Erratum (DOI:10.1016/j.amjoto.2005.09.007);Cochlear nerve size evaluation in children with sensorineural hearing loss by high-resolution magnetic resonance imaging

American Journal of Otolaryngology - Head and Neck Medicine and Surgery

Volumn 27, Issue 3, 2006, Pages 166-172

  Russo, Eyal E ^a   Manolidis, Spiros ^b  

^a TEXAS CHILDREN S HOSPITAL   (United States)

^b Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26;

ACCURACY; ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; COCHLEA; COCHLEAR NERVE; COMPARATIVE STUDY; COMPUTED TOMOGRAPHIC ANGIOGRAPHY; CONTROLLED STUDY; EVALUATION; FEMALE; GENE MUTATION; HEARING; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; HYPOPLASIA; IN VIVO STUDY; INNER EAR; INTERMETHOD COMPARISON; INTERNAL AUDITORY CANAL; MALE; MEASUREMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTICAL RESOLUTION; PEDIATRICS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; TEMPORAL BONE; TISSUE SECTION; VOLUMETRY;

EID: 33646093453     PISSN: 01960709     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjoto.2007.01.003     Document Type: Erratum

References (21)

1. Greinwald Jr. J.H., and Hartnick C.J. The evaluation of children with sensorineural hearing loss. Arch Otolaryngol Head Neck Surg 128 (2002) 84-87
2. Morton N.E. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci 630 (1991) 16-31
3. Kenna M.A., Wu B.L., Cotanche D.A., et al. Connexin 26 studies in patients with sensorineural hearing loss. Arch Otolaryngol Head Neck Surg 127 (2001) 1037-1042
4. Jun A.I., McGuirt W.T., Hinojosa R., et al. Temporal bone histopathology in connexin 26-related hearing loss. Laryngoscope 110 (2000) 269-275
5. Oghalai J.S., Chen L., Brennan M.L., et al. Neonatal hearing loss in the indigent. Laryngoscope 112 (2002) 281-286
6. McClay J.E., Tandy R., Grundfast K., et al. Major and minor temporal bone abnormalities in children with and without congenital sensorineural hearing loss. Arch Otolaryngol Head Neck Surg 128 (2002) 664-671
7. Park A.H., Kou B., Hotaling A., et al. Clinical course of pediatric congenital inner ear malformations. Laryngoscope 110 (2000) 1715-1719
8. Casselman J.W. Diagnostic imaging in clinical neuro-otology. Curr Opin Neurol 15 (2002) 23-30
9. Casselman J.W., Offeciers F.E., Govaerts P.J., et al. Aplasia and hypoplasia of the vestibulocochlear nerve: diagnosis with MR imaging. Radiology 202 (1997) 773-781
10. Murugasu E., Hans P., Jackson A., et al. The application of three-dimensional magnetic resonance imaging rendering of the inner ear in assessment for cochlear implantation. Am J Otolaryngol 20 (1999) 752-757
11. Casselman J.W., Kuhweide R., Ampe W., et al. Inner ear malformations in patients with sensorineural hearing loss: detection with gradient-echo (3DFT-CISS) MRI. Neuroradiology 38 (1996) 278-286
12. Casselman J.W., Offeciers E.F., De Foer B., et al. CT and MR imaging of congenital abnormalities of the inner ear and internal auditory canal. Eur J Radiol 40 (2001) 94-104
13. Casselman J.W. Advanced sequences improve evaluation of temporal bone disease. Diagn Imaging (San Franc) 22 (2000) 172-177
14. Chan L.L., Manolidis S., Taber K.H., et al. Surgical anatomy of the temporal bone: an atlas. Neuroradiology 43 (2001) 797-808
15. Chan L.L., Manolidis S., Taber K.H., et al. In vivo measurements of temporal bone on reconstructed clinical high-resolution computed tomography scans. Laryngoscope 110 (2000) 1375-1378
16. Grundfast KM, Lalwani AK. Practical approach to diagnosis and management of hereditary hearing impairment (HHI). Ear Nose Throat J 1992;71: 479-84, 487-93.
17. Furuta S., Ogura M., Higano S., et al. Reduced size of the cochlear branch of the vestibulocochlear nerve in a child with sensorineural hearing loss. AJNR Am J Neuroradiol 21 (2000) 328-330
18. Maxwell A.P., Mason S.M., and O'Donoghue G.M. Cochlear nerve aplasia: its importance in cochlear implantation. Am J Otolaryngol 20 (1999) 335-337
19. Guilford P., Ben Arab S., Blanchard S., et al. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nat Genet 6 (1994) 24-28
20. Kelsell D.P., Dunlop J., Stevens H.P., et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 387 (1997) 80-83
21. Green G.E., Scott D.A., McDonald J.M., et al. Carrier rates in the Midwestern United States for GJB2 mutations causing inherited deafness. JAMA 281 (1999) 2211-2216