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Volumn 110, Issue 5 I, 2000, Pages 787-798

Analysis of a cohort of children with sensory hearing loss using the SCALE systematic nomenclature

Author keywords

Connexin 26 etiology; Deafness; Hearing loss; Nomenclature

Indexed keywords

CONNEXIN 26;

EID: 0034065560     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-200005000-00009     Document Type: Article
Times cited : (19)

References (26)
  • 1
    • 0024563249 scopus 로고
    • Congenital perilymphatic fistula: A prospective study in infants and children
    • Reilly JS. Congenital perilymphatic fistula: a prospective study in infants and children. Laryngoscope 1989;99:393-397.
    • (1989) Laryngoscope , vol.99 , pp. 393-397
    • Reilly, J.S.1
  • 2
    • 0030034841 scopus 로고    scopus 로고
    • Aetiology of bilateral sensorineural hearing impairment in children: A 10 year study
    • Das VK. Aetiology of bilateral sensorineural hearing impairment in children: a 10 year study. Arch Dis Child 1996;74(1): 8-12.
    • (1996) Arch Dis Child , vol.74 , Issue.1 , pp. 8-12
    • Das, V.K.1
  • 3
    • 0032925740 scopus 로고    scopus 로고
    • Causes of pediatric sensorineural hearing loss: Yesterday and today
    • Billings KR, Kenna MA. Causes of pediatric sensorineural hearing loss: yesterday and today. Arch Otolaryngol Head Neck Surg 1999;125(5):517-521.
    • (1999) Arch Otolaryngol Head Neck Surg , vol.125 , Issue.5 , pp. 517-521
    • Billings, K.R.1    Kenna, M.A.2
  • 4
    • 0033064890 scopus 로고    scopus 로고
    • Prevalence and characteristics of children with serious hearing impairment in metropolitan Atlanta: 1991-1993
    • Van Naarden K, Decoufle P, Caldwell K. Prevalence and characteristics of children with serious hearing impairment in metropolitan Atlanta: 1991-1993 Pediatrics 1999; 103(3):570-575.
    • (1999) Pediatrics , vol.103 , Issue.3 , pp. 570-575
    • Van Naarden, K.1    Decoufle, P.2    Caldwell, K.3
  • 5
    • 0242338200 scopus 로고
    • Hereditary deafness in man
    • Konigsmark BW. Hereditary deafness in man. N Engl J Med 1969;281:713-720, 774-778, 827-832.
    • (1969) N Engl J Med , vol.281 , pp. 713-720
    • Konigsmark, B.W.1
  • 7
    • 0033524936 scopus 로고    scopus 로고
    • KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
    • Kubisch C, Schroeder BC, Friedrich T, et al. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell 1999;96(3):437-446.
    • (1999) Cell , vol.96 , Issue.3 , pp. 437-446
    • Kubisch, C.1    Schroeder, B.C.2    Friedrich, T.3
  • 8
    • 0033511445 scopus 로고    scopus 로고
    • Newborn hearing screening: Will children with hearing loss caused by congenital cytomegalovirus infection be missed?
    • Fowler KB, Dahle AJ, Boppana SB, Pass RF. Newborn hearing screening: will children with hearing loss caused by congenital cytomegalovirus infection be missed? J Pediatr 1999;135(1):60-64.
    • (1999) J Pediatr , vol.135 , Issue.1 , pp. 60-64
    • Fowler, K.B.1    Dahle, A.J.2    Boppana, S.B.3    Pass, R.F.4
  • 9
    • 0031943310 scopus 로고    scopus 로고
    • Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome
    • Cremers WR, Otten BJ, Green ED, et al. Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome. Arch Otolaryngol Head Neck Surg 1998;124(5):501-505.
    • (1998) Arch Otolaryngol Head Neck Surg , vol.124 , Issue.5 , pp. 501-505
    • Cremers, W.R.1    Otten, B.J.2    Green, E.D.3
  • 10
    • 0033062827 scopus 로고    scopus 로고
    • Pendred's syndrome: Identification of the genetic defect a century after its recognition
    • Kopp P. Pendred's syndrome: identification of the genetic defect a century after its recognition. Thyroid 1999;9(1):65-69.
    • (1999) Thyroid , vol.9 , Issue.1 , pp. 65-69
    • Kopp, P.1
  • 11
    • 0032011145 scopus 로고    scopus 로고
    • A mutation in pds causes non-syndromic recessive deafness
    • Li XC, Everett LA, Lalwani AK, et al. A mutation in PDS causes non-syndromic recessive deafness. Nat Genet 1998; 18(3):215-217.
    • (1998) Nat Genet , vol.18 , Issue.3 , pp. 215-217
    • Li, X.C.1    Everett, L.A.2    Lalwani, A.K.3
  • 12
    • 0027226069 scopus 로고
    • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and nonsyndromic deafness
    • Prezant TR, Agapian JV, Bohlman C, et al. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and nonsyndromic deafness. Nat Genet 1993;4: 289-294.
    • (1993) Nat Genet , vol.4 , pp. 289-294
    • Prezant, T.R.1    Agapian, J.V.2    Bohlman, C.3
  • 13
    • 0342944590 scopus 로고    scopus 로고
    • Association for research in otoloaryngology: Next 25 years
    • 25th Anniversary Special Edition, February
    • Peter Dallos. Association for Research in Otoloaryngology: next 25 years. ARO Newsletter. 25th Anniversary Special Edition, February 1998, pp 1-4.
    • (1998) ARO Newsletter , pp. 1-4
    • Dallos, P.1
  • 14
    • 0030777198 scopus 로고    scopus 로고
    • Response of the primary auditory cortex to electrical stimulation of the auditory nerve in the congenitally deaf white cat
    • Hartmann R, Shepherd RK, Heid S, Klinke R. Response of the primary auditory cortex to electrical stimulation of the auditory nerve in the congenitally deaf white cat. Hear Res 1997;112(1-2):115-133.
    • (1997) Hear Res , vol.112 , Issue.1-2 , pp. 115-133
    • Hartmann, R.1    Shepherd, R.K.2    Heid, S.3    Klinke, R.4
  • 15
    • 0032837708 scopus 로고    scopus 로고
    • Conductive hearing loss: Results in a decrease in central auditory system activity in the young gerbil
    • Tucci DL, Cant NB, Durham D. Conductive hearing loss: results in a decrease in central auditory system activity in the young gerbil. Laryngoscope 1999;109(9):1359-1370.
    • (1999) Laryngoscope , vol.109 , Issue.9 , pp. 1359-1370
    • Tucci, D.L.1    Cant, N.B.2    Durham, D.3
  • 16
    • 0033025481 scopus 로고    scopus 로고
    • Cochlear implantation in children with enlarged vestibular aqueducts
    • Bent JP 3rd, Chute P, Parisier SC. Cochlear implantation in children with enlarged vestibular aqueducts Laryngoscope 1999;109:1019-1022.
    • (1999) Laryngoscope , vol.109 , pp. 1019-1022
    • Bent J.P. III1    Chute, P.2    Parisier, S.C.3
  • 17
    • 0342510373 scopus 로고
    • Baltimore: Williams & Wilkins
    • John Ballantyne. Deafness. edn 2. Baltimore: Williams & Wilkins, 1970:1.
    • (1970) Deafness. Edn 2. , pp. 1
    • Ballantyne, J.1
  • 19
    • 0029990045 scopus 로고    scopus 로고
    • Optiz G/BBB syndrome; clinical comparisons of families linked to Xp22 and 22q, and a review of the literature
    • Robin NH, Opitz JM, Muenke M. Optiz G/BBB syndrome; clinical comparisons of families linked to Xp22 and 22q, and a review of the literature. Am J Med Genet 1996;62: 305-317.
    • (1996) Am J Med Genet , vol.62 , pp. 305-317
    • Robin, N.H.1    Opitz, J.M.2    Muenke, M.3
  • 21
    • 0031759971 scopus 로고    scopus 로고
    • Noonan's syndrome with sensorineural hearing loss and vestibular abnormalities
    • Foster CA, Dyhrkopp PJ. Noonan's syndrome with sensorineural hearing loss and vestibular abnormalities. Otolaryngol Head Neck Surg 1998;119(5):508-511.
    • (1998) Otolaryngol Head Neck Surg , vol.119 , Issue.5 , pp. 508-511
    • Foster, C.A.1    Dyhrkopp, P.J.2
  • 23
    • 0030812608 scopus 로고    scopus 로고
    • Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection
    • Fowler KB, McCollister FP, Dahle AJ, Boppana S, Britt WJ, Pass RF. Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection. J Pediatr 1997;130(4):624-630.
    • (1997) J Pediatr , vol.130 , Issue.4 , pp. 624-630
    • Fowler, K.B.1    McCollister, F.P.2    Dahle, A.J.3    Boppana, S.4    Britt, W.J.5    Pass, R.F.6
  • 24
    • 0033577528 scopus 로고    scopus 로고
    • Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: Implications for genetic counselling
    • Denoyelle F, Marlin S, Weil D, et al. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling. Lancet 1999;353:1298-1303.
    • (1999) Lancet , vol.353 , pp. 1298-1303
    • Denoyelle, F.1    Marlin, S.2    Weil, D.3
  • 25
    • 0032987903 scopus 로고    scopus 로고
    • Genetic deafness: A step closer
    • Steel KP. Genetic deafness: a step closer [comment]. Pediatrics 1999;103(3):674.
    • (1999) Pediatrics , vol.103 , Issue.3 , pp. 674
    • Steel, K.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.