-
3
-
-
37349038234
-
Hemifacial microsomia: Clinical features and pictographic representations of the OMENS classification system
-
Gougoutas AJ, Singh DJ, Low DW, et al. Hemifacial microsomia: clinical features and pictographic representations of the OMENS classification system. Plast Reconstr Surg 2007;120:112e-20e.
-
(2007)
Plast. Reconstr. Surg.
, vol.120
-
-
Gougoutas, A.J.1
Singh, D.J.2
Low, D.W.3
-
4
-
-
0024365875
-
The association of facial palsy and/or sensorineural hearing loss in patients with hemifacial microsomia
-
Bassila MK, Goldberg R. The association of facial palsy and/or sensorineural hearing loss in patients with hemifacial microsomia. Cleft Palate J 1989;26:287-91.
-
(1989)
Cleft Palate J.
, vol.26
, pp. 287-291
-
-
Bassila, M.K.1
Goldberg, R.2
-
5
-
-
0028836532
-
Microtia and significant auricular malformation. Ninetytwo pediatric patients
-
Eavey RD. Microtia and significant auricular malformation. Ninetytwo pediatric patients. Arch Otolaryngol Head Neck Surg 1995;121:57-62.
-
(1995)
Arch. Otolaryngol. Head Neck Surg.
, vol.121
, pp. 57-62
-
-
Eavey, R.D.1
-
7
-
-
0035097908
-
Craniofacial, temporal bone, and audiologic abnormalities in the spectrum of hemifacial microsomia
-
Rahbar R, Robson CD, Mulliken JB, et al. Craniofacial, temporal bone, and audiologic abnormalities in the spectrum of hemifacial microsomia. Arch Otolaryngol Head Neck Surg 2001;127:265-71.
-
(2001)
Arch. Otolaryngol. Head Neck Surg.
, vol.127
, pp. 265-271
-
-
Rahbar, R.1
Robson, C.D.2
Mulliken, J.B.3
-
8
-
-
0014298526
-
Inner ear anomalies: Their association with atresia
-
Naunton RF, Valvassori GE. Inner ear anomalies: their association with atresia. Laryngoscope 1968;78:1041-9.
-
(1968)
Laryngoscope
, vol.78
, pp. 1041-1049
-
-
Naunton, R.F.1
Valvassori, G.E.2
-
9
-
-
0016221725
-
Congenital lesions of the inner ear, demonstrated by tomography
-
Phelps PD. Congenital lesions of the inner ear, demonstrated by tomography. Arch Otolaryngol 1974;100:11-8.
-
(1974)
Arch. Otolaryngol.
, vol.100
, pp. 11-18
-
-
Phelps, P.D.1
-
10
-
-
0031032028
-
High-resolution CT of the temporal bone in dysplasia of the auricle and external auditory canal
-
Mayer TE, Brueckmann H, Siegert R, et al. High-resolution CT of the temporal bone in dysplasia of the auricle and external auditory canal. AJNR Am J Neuroradiol 1997;18:53-65.
-
(1997)
AJNR Am. J. Neuroradiol.
, vol.18
, pp. 53-65
-
-
Mayer, T.E.1
Brueckmann, H.2
Siegert, R.3
-
11
-
-
33746781363
-
Two temporal bone computed tomography measurements increase recognition of malformations and predict sensorineural hearing loss
-
Purcell DD, Fischbein NJ, Patel A, et al. Two temporal bone computed tomography measurements increase recognition of malformations and predict sensorineural hearing loss. Laryngoscope 2006;116:1439-46.
-
(2006)
Laryngoscope
, vol.116
, pp. 1439-1446
-
-
Purcell, D.D.1
Fischbein, N.J.2
Patel, A.3
-
13
-
-
0026527396
-
Grading system for the selection of patients with congenital aural atresia
-
Jahrsdoerfer RA, Yeakley JW, Aguilar EA, et al. Grading system for the selection of patients with congenital aural atresia. Am J Otol 1992;13:6-12.
-
(1992)
Am. J. Otol.
, vol.13
, pp. 6-12
-
-
Jahrsdoerfer, R.A.1
Yeakley, J.W.2
Aguilar, E.A.3
-
14
-
-
41349104942
-
Conductive hearing loss caused by third-window lesions of the inner ear
-
Merchant SN, Rosowski JJ. Conductive hearing loss caused by third-window lesions of the inner ear. Otol Neurotol 2008;29:282-9.
-
(2008)
Otol. Neurotol
, vol.29
, pp. 282-289
-
-
Merchant, S.N.1
Rosowski, J.J.2
-
15
-
-
0014532934
-
Inner ear abnormalities in association with congenital atresia of the external auditory canal, including a case of Michel deformity
-
Potter GD. Inner ear abnormalities in association with congenital atresia of the external auditory canal, including a case of Michel deformity. Ann Otol Rhinol Laryngol 1969;78:598-604.
-
(1969)
Ann. Otol. Rhinol. Laryngol.
, vol.78
, pp. 598-604
-
-
Potter, G.D.1
-
16
-
-
0345529104
-
Molecular genetic advances in semicircular canal abnormalities and sensorineural hearing loss: A report of 16 cases
-
Yu KK, Mukherji S, Carrasco V, et al. Molecular genetic advances in semicircular canal abnormalities and sensorineural hearing loss: a report of 16 cases. Otolaryngol Head Neck Surg 2003;129:637-46.
-
(2003)
Otolaryngol. Head Neck Surg.
, vol.129
, pp. 637-646
-
-
Yu, K.K.1
Mukherji, S.2
Carrasco, V.3
-
19
-
-
33746925573
-
Partial absence of the posterior semicircular canal in Alagille syndrome: CT findings
-
Koch B, Goold A, Egelhoff J, et al. Partial absence of the posterior semicircular canal in Alagille syndrome: CT findings. Pediatr Radiol 2006;36:977-9.
-
(2006)
Pediatr. Radiol.
, vol.36
, pp. 977-979
-
-
Koch, B.1
Goold, A.2
Egelhoff, J.3
-
20
-
-
0021345232
-
Congenital sensorineural hearing loss
-
Mafee MF, Selis JE, Yannias DA, et al. Congenital sensorineural hearing loss. Radiology 1984;150:427-34.
-
(1984)
Radiology
, vol.150
, pp. 427-434
-
-
Mafee, M.F.1
Selis, J.E.2
Yannias, D.A.3
-
21
-
-
0026675412
-
Aplasia of posterior semicircular canal in Waardenburg syndrome type II
-
Higashi K, Matsuki C, Sarashina N. Aplasia of posterior semicircular canal in Waardenburg syndrome type II. J Otolaryngol 1992;21:262-4.
-
(1992)
J. Otolaryngol.
, vol.21
, pp. 262-264
-
-
Higashi, K.1
Matsuki, C.2
Sarashina, N.3
-
22
-
-
33845499720
-
Inner ear dysplasia is common in children with Down syndrome (trisomy 21)
-
Blaser S, Propst EJ, Martin D, et al. Inner ear dysplasia is common in children with Down syndrome (trisomy 21). Laryngoscope 2006;116:2113-9.
-
(2006)
Laryngoscope
, vol.116
, pp. 2113-2119
-
-
Blaser, S.1
Propst, E.J.2
Martin, D.3
-
23
-
-
77649225132
-
Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome
-
Zentner GE, Layman WS, Martin DM, et al. Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. Am J Med Genet A 2010;152 A: 674-86.
-
(2010)
Am. J. Med. Genet. A
, vol.152 A
, pp. 674-686
-
-
Zentner, G.E.1
Layman, W.S.2
Martin, D.M.3
-
24
-
-
33846615392
-
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia
-
Tekin M, Hişmi BO, Fitoz S, et al. Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia. Am J Hum Genet 2007;80:338-44.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 338-344
-
-
Tekin, M.1
Hişmi, B.O.2
Fitoz, S.3
-
26
-
-
67449111228
-
Genetics of microtia and associated syndromes
-
Alasti F, Van Camp G. Genetics of microtia and associated syndromes. J Med Genet 2009;46:361-9.
-
(2009)
J. Med. Genet.
, vol.46
, pp. 361-369
-
-
Alasti, F.1
Van Camp, G.2
-
27
-
-
36049011251
-
The first steps towards hearing: Mechanisms of otic placode induction
-
Ohyama T, Groves AK, Martin K. The first steps towards hearing: mechanisms of otic placode induction. Int J Dev Biol 2007;51:463-72.
-
(2007)
Int. J. Dev. Biol.
, vol.51
, pp. 463-472
-
-
Ohyama, T.1
Groves, A.K.2
Martin, K.3
-
28
-
-
36049041278
-
A network of growth and transcription factors controls neuronal differentiation and survival in the developing ear
-
Sanchez-Calderon H, Milo M, Leon Y, et al. A network of growth and transcription factors controls neuronal differentiation and survival in the developing ear. Int J Dev Biol 2007;51:557-70.
-
(2007)
Int. J. Dev. Biol.
, vol.51
, pp. 557-570
-
-
Sanchez-Calderon, H.1
Milo, M.2
Leon, Y.3
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