-
1
-
-
52949130567
-
Joint statement on neonatal screening for hearing impairment
-
Committee on Fetus and Newborn. Joint statement on neonatal screening for hearing impairment. Pediatrics 47 6 (1971) 1085
-
(1971)
Pediatrics
, vol.47
, Issue.6
, pp. 1085
-
-
Committee on Fetus and Newborn1
-
2
-
-
0020430853
-
Joint Committee on Infant Hearing position statement
-
Joint Committee on Infant Hearing position statement. ASHA 24 12 (1982) 1017-1018
-
(1982)
ASHA
, vol.24
, Issue.12
, pp. 1017-1018
-
-
-
3
-
-
0027565992
-
Early identification of hearing impairment in infants and young children
-
Early identification of hearing impairment in infants and young children. National Institutes of Health Consensus conference statement. 11 (1993) 1-24
-
(1993)
National Institutes of Health Consensus conference statement.
, vol.11
, pp. 1-24
-
-
-
5
-
-
0031728855
-
Language of early- and later-identified children with hearing loss
-
Yoshinaga-Itano C., Sedey A.L., Coulter D.K., et al. Language of early- and later-identified children with hearing loss. Pediatrics 102 5 (1998) 1161-1171
-
(1998)
Pediatrics
, vol.102
, Issue.5
, pp. 1161-1171
-
-
Yoshinaga-Itano, C.1
Sedey, A.L.2
Coulter, D.K.3
-
6
-
-
0032936357
-
The efficacy of early identification and intervention for children with hearing impairment
-
Downs M.P., and Yoshinaga-Itano C. The efficacy of early identification and intervention for children with hearing impairment. Pediatr Clin North Am 46 1 (1999) 79-87
-
(1999)
Pediatr Clin North Am
, vol.46
, Issue.1
, pp. 79-87
-
-
Downs, M.P.1
Yoshinaga-Itano, C.2
-
7
-
-
0347382300
-
Early intervention after universal neonatal hearing screening: impact on outcomes
-
Yoshinaga-Itano C. Early intervention after universal neonatal hearing screening: impact on outcomes. Ment Retard Dev Disabil Res Rev 9 4 (2003) 252-266
-
(2003)
Ment Retard Dev Disabil Res Rev
, vol.9
, Issue.4
, pp. 252-266
-
-
Yoshinaga-Itano, C.1
-
8
-
-
35148846825
-
Year 2007 position statement: principles and guidelines for early hearing detection and intervention program
-
Joint Committee on Infant Hearing. Year 2007 position statement: principles and guidelines for early hearing detection and intervention program. Pediatrics 120 4 (2007) 898-921
-
(2007)
Pediatrics
, vol.120
, Issue.4
, pp. 898-921
-
-
Joint Committee on Infant Hearing1
-
9
-
-
0242491485
-
Evidence of surviving outer hair cell function in congenitally deaf ears
-
Rea P.A., and Gibson W.P. Evidence of surviving outer hair cell function in congenitally deaf ears. Laryngoscope 113 (2003) 2030-2034
-
(2003)
Laryngoscope
, vol.113
, pp. 2030-2034
-
-
Rea, P.A.1
Gibson, W.P.2
-
10
-
-
13844264405
-
A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells
-
Starr A., Isaacson B., Michaelewski H., et al. A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells. J Assoc Res Otolaryngol 5 (2004) 411-426
-
(2004)
J Assoc Res Otolaryngol
, vol.5
, pp. 411-426
-
-
Starr, A.1
Isaacson, B.2
Michaelewski, H.3
-
11
-
-
0002772201
-
Pathophysiology of auditory neuropathy
-
Sininger Y., and Starr A. (Eds), Singular-Thomson Learning, San Diego (CA)
-
Starr A., Picton T.W., and Kim R. Pathophysiology of auditory neuropathy. In: Sininger Y., and Starr A. (Eds). Auditory neuropathy: new perspectives in hearing disorders (2001), Singular-Thomson Learning, San Diego (CA) 67-82
-
(2001)
Auditory neuropathy: new perspectives in hearing disorders
, pp. 67-82
-
-
Starr, A.1
Picton, T.W.2
Kim, R.3
-
12
-
-
20344401075
-
Auditory neuropathy/dys-synchrony and its perceptual consequences
-
Rance G. Auditory neuropathy/dys-synchrony and its perceptual consequences. Trends Amplif 9 (2005) 1-43
-
(2005)
Trends Amplif
, vol.9
, pp. 1-43
-
-
Rance, G.1
-
13
-
-
33646372039
-
Clinical applications of OAEs in children
-
Danhauer JL. (Ed), Singular-Thomson Learning, San Diego (CA)
-
Hall III J.W. Clinical applications of OAEs in children. In: Danhauer JL. (Ed). Handbook of otoacoustic emissions (2000), Singular-Thomson Learning, San Diego (CA) 389-480
-
(2000)
Handbook of otoacoustic emissions
, pp. 389-480
-
-
Hall III, J.W.1
-
14
-
-
0038157208
-
Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (tyr145→Ser)
-
Starr A., Michaelewski H.J., Zeng F.-G., et al. Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (tyr145→Ser). Brain 126 (2003) 1604-1619
-
(2003)
Brain
, vol.126
, pp. 1604-1619
-
-
Starr, A.1
Michaelewski, H.J.2
Zeng, F.-G.3
-
16
-
-
0018933647
-
Auditory dysfunction in Friedreich ataxia: result of spiral ganglion degeneration
-
Satya-Murti S., Cacace A., and Hanson P. Auditory dysfunction in Friedreich ataxia: result of spiral ganglion degeneration. Neurology 30 (1980) 1047-1053
-
(1980)
Neurology
, vol.30
, pp. 1047-1053
-
-
Satya-Murti, S.1
Cacace, A.2
Hanson, P.3
-
17
-
-
0035099018
-
Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies
-
Zwirner P., and Wilichowski E. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies. Laryngoscope 111 (2001) 515-521
-
(2001)
Laryngoscope
, vol.111
, pp. 515-521
-
-
Zwirner, P.1
Wilichowski, E.2
-
18
-
-
0028962606
-
Sensorineural hearing loss in patients with large vestibular aqueduct
-
Okumura T., Takahashi H., Honjo I., et al. Sensorineural hearing loss in patients with large vestibular aqueduct. Laryngoscope 105 (1995) 289-294
-
(1995)
Laryngoscope
, vol.105
, pp. 289-294
-
-
Okumura, T.1
Takahashi, H.2
Honjo, I.3
-
19
-
-
0032133117
-
Large vestibular aqueduct syndrome: an overlooked etiology for progressive childhood hearing loss
-
Callison D.M., and Horn K.L. Large vestibular aqueduct syndrome: an overlooked etiology for progressive childhood hearing loss. J Am Acad Audiol 9 (1998) 285-291
-
(1998)
J Am Acad Audiol
, vol.9
, pp. 285-291
-
-
Callison, D.M.1
Horn, K.L.2
-
20
-
-
52949132190
-
National Institutes for Deafness and Other Communication Disorders
-
Accessed April 16, 2008
-
National Institutes for Deafness and Other Communication Disorders. Pendred syndrome. (2007). http://www.nidcd.nih.gov/health/hearing/ Accessed April 16, 2008
-
(2007)
Pendred syndrome.
-
-
-
21
-
-
52949084619
-
-
Accessed April 16, 2008
-
Smith R., and Van Camp G. Pendred syndrome/DFN4 (2006). Available at: http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=gene.chapter.pendred Accessed April 16, 2008
-
(2006)
Pendred syndrome/DFN4
-
-
Smith, R.1
Van Camp, G.2
-
22
-
-
13444254030
-
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities
-
Pryor S.P., Madeo A.C., Reynolds J.C., et al. SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities. J Med Genet 42 (2005) 159-165
-
(2005)
J Med Genet
, vol.42
, pp. 159-165
-
-
Pryor, S.P.1
Madeo, A.C.2
Reynolds, J.C.3
-
23
-
-
34447521956
-
Clinical investigation and mechanism of air-bone gaps in large aqueduct syndrome
-
Merchant S.N., Nakajima H.H., Halpin C., et al. Clinical investigation and mechanism of air-bone gaps in large aqueduct syndrome. Ann Otol Rhinol Laryngol 116 (2007) 532-541
-
(2007)
Ann Otol Rhinol Laryngol
, vol.116
, pp. 532-541
-
-
Merchant, S.N.1
Nakajima, H.H.2
Halpin, C.3
-
24
-
-
12144287717
-
A genotype-phenotype correlation for GBJ2 (connexin 26) deafness
-
Cyrns K., Orzan E., Murgia A., et al. A genotype-phenotype correlation for GBJ2 (connexin 26) deafness. J Med Genet 41 (2004) 147-154
-
(2004)
J Med Genet
, vol.41
, pp. 147-154
-
-
Cyrns, K.1
Orzan, E.2
Murgia, A.3
-
25
-
-
0033037643
-
Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)
-
Cohn E.S., Kelley P.M., Fowler T.W., et al. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1). Pediatrics 103 (1999) 546-550
-
(1999)
Pediatrics
, vol.103
, pp. 546-550
-
-
Cohn, E.S.1
Kelley, P.M.2
Fowler, T.W.3
-
26
-
-
14744282666
-
Sensorineural hearing loss in children
-
Smith R.J., Bale J.F., and White K.R. Sensorineural hearing loss in children. Lancet 365 (2005) 879-890
-
(2005)
Lancet
, vol.365
, pp. 879-890
-
-
Smith, R.J.1
Bale, J.F.2
White, K.R.3
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