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Results: 1 to 20 of 103

Similar articles for PubMed (Select 18580690)

1.

Infant hearing loss and connexin testing in a diverse population.

Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CG.

Genet Med. 2008 Jul;10(7):517-24. doi: 10.1097GIM.0b013e31817708fa.

PMID:
18580690
2.

Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss.

Erbe CB, Harris KC, Runge-Samuelson CL, Flanary VA, Wackym PA.

Laryngoscope. 2004 Apr;114(4):607-11.

PMID:
15064611
3.

Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.

Norris VW, Arnos KS, Hanks WD, Xia X, Nance WE, Pandya A.

Ear Hear. 2006 Dec;27(6):732-41.

PMID:
17086082
4.

Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening.

Schimmenti LA, Warman B, Schleiss MR, Daly KA, Ross JA, McCann M, Jurek AM, Berry SA.

Genet Med. 2011 Dec;13(12):1006-10. doi: 10.1097/GIM.0b013e318226fc2e.

PMID:
21912263
5.

[Audiologic and molecular screening for hearing loss by 35delG mutation in connexin 26 gene and congenital cytomegalovirus infection].

Streitenberger ER, Suárez AI, Masciovecchio MV, Laurnagaray D, Alda E.

Arch Argent Pediatr. 2011 Dec;109(6):479-84. doi: 10.1590/S0325-00752011000600003. Spanish.

6.

A multicenter evaluation of how many infants with permanent hearing loss pass a two-stage otoacoustic emissions/automated auditory brainstem response newborn hearing screening protocol.

Johnson JL, White KR, Widen JE, Gravel JS, James M, Kennalley T, Maxon AB, Spivak L, Sullivan-Mahoney M, Vohr BR, Weirather Y, Holstrum J.

Pediatrics. 2005 Sep;116(3):663-72.

PMID:
16140706
7.

[Prospects for genetic hearing loss screening: 35delG mutation tracking in a newborn population].

Piatto VB, Oliveira CA, Alexandrino F, Pimpinati CJ, Sartorato EL.

J Pediatr (Rio J). 2005 Mar-Apr;81(2):139-42. Portuguese.

8.

Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.

Kenna MA, Feldman HA, Neault MW, Frangulov A, Wu BL, Fligor B, Rehm HL.

Arch Otolaryngol Head Neck Surg. 2010 Jan;136(1):81-7. doi: 10.1001/archoto.2009.202.

PMID:
20083784
9.

Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations.

Santos RL, Aulchenko YS, Huygen PL, van der Donk KP, de Wijs IJ, Kemperman MH, Admiraal RJ, Kremer H, Hoefsloot LH, Cremers CW.

Int J Pediatr Otorhinolaryngol. 2005 Feb;69(2):165-74.

PMID:
15656949
10.

Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening.

Lü J, Huang Z, Yang T, Li Y, Mei L, Xiang M, Chai Y, Li X, Li L, Yao G, Wang Y, Shen X, Wu H.

Int J Pediatr Otorhinolaryngol. 2011 Aug;75(8):1045-9. doi: 10.1016/j.ijporl.2011.05.022. Epub 2011 Jun 25.

PMID:
21705096
12.

GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review.

Kenneson A, Van Naarden Braun K, Boyle C.

Genet Med. 2002 Jul-Aug;4(4):258-74. Review.

PMID:
12172392
13.

Absence of GJB6 mutations in Indian patients with non-syndromic hearing loss.

Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.

Int J Pediatr Otorhinolaryngol. 2011 Mar;75(3):356-9. doi: 10.1016/j.ijporl.2010.12.003. Epub 2011 Jan 11.

PMID:
21227513
14.

Newborn hearing screening on infants at risk.

Ohl C, Dornier L, Czajka C, Chobaut JC, Tavernier L.

Int J Pediatr Otorhinolaryngol. 2009 Dec;73(12):1691-5. doi: 10.1016/j.ijporl.2009.08.027. Epub 2009 Sep 30.

PMID:
19796829
15.

Identification of neonatal hearing impairment: infants with hearing loss.

Cone-Wesson B, Vohr BR, Sininger YS, Widen JE, Folsom RC, Gorga MP, Norton SJ.

Ear Hear. 2000 Oct;21(5):488-507.

PMID:
11059706
16.

Connexin 26 deafness is not always congenital.

Orzan E, Murgia A.

Int J Pediatr Otorhinolaryngol. 2007 Mar;71(3):501-7. Epub 2007 Jan 11.

PMID:
17222463
17.

Methodology of a multistate study of congenital hearing loss: preliminary data from Utah newborn screening.

Dent KM, Kenneson A, Palumbos JC, Maxwell S, Eichwald J, White K, Mao R, Bale JF Jr, Carey JC.

Am J Med Genet C Semin Med Genet. 2004 Feb 15;125C(1):28-34.

PMID:
14755431
18.

A multisite study to examine the efficacy of the otoacoustic emission/automated auditory brainstem response newborn hearing screening protocol: research design and results of the study.

White KR, Vohr BR, Meyer S, Widen JE, Johnson JL, Gravel JS, James M, Kennalley T, Maxon AB, Spivak L, Sullivan-Mahoney M, Weirather Y.

Am J Audiol. 2005 Dec;14(2):S186-199.

PMID:
16489863
19.

GJB2 mutations in the Swiss hearing impaired.

Gürtler N, Kim Y, Mhatre A, Müller R, Probst R, Lalwani AK.

Ear Hear. 2003 Oct;24(5):440-7.

PMID:
14534413
20.

Connexin 26 studies in patients with sensorineural hearing loss.

Kenna MA, Wu BL, Cotanche DA, Korf BR, Rehm HL.

Arch Otolaryngol Head Neck Surg. 2001 Sep;127(9):1037-42.

PMID:
11556849
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