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3. Clinical Practice Guideline: Sudden Hearing Loss (Update). Chandrasekhar SS; Tsai Do BS; Schwartz SR; Bontempo LJ; Faucett EA; Finestone SA; Hollingsworth DB; Kelley DM; Kmucha ST; Moonis G; Poling GL; Roberts JK; Stachler RJ; Zeitler DM; Corrigan MD; Nnacheta LC; Satterfield L Otolaryngol Head Neck Surg; 2019 Aug; 161(1_suppl):S1-S45. PubMed ID: 31369359 [TBL] [Abstract][Full Text] [Related]
4. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria]. Gallo-Terán J; Morales-Angulo C; del Castillo I; Villamar M; Moreno-Pelayo MA; García-Mantilla J; Moreno F Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196 [TBL] [Abstract][Full Text] [Related]
5. [The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life]. Lalaiants MR; Bliznets EA; Markova TG; Poliakov AV; Tavartkiladze GA Vestn Otorinolaringol; 2011; (3):31-5. PubMed ID: 21720291 [TBL] [Abstract][Full Text] [Related]
6. Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Gao Y; Wang HY; Guan J; Lan L; Zhao C; Xie LY; Wang DY; Wang QJ Curr Med Sci; 2021 Aug; 41(4):673-679. PubMed ID: 34403091 [TBL] [Abstract][Full Text] [Related]
7. [The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]. Lalaiants MR; Markova TG; Bakhshinian VV; Bliznets EA; Poliakov AV; Tavartikiladze GA Vestn Otorinolaringol; 2014; (2):37-43. PubMed ID: 24781170 [TBL] [Abstract][Full Text] [Related]
9. Sudden hearing loss in a family with GJB2 related progressive deafness. Kokotas H; Theodosiou M; Korres G; Grigoriadou M; Ferekidou E; Giannoulia-Karantana A; Petersen MB; Korres S Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1735-40. PubMed ID: 18809215 [TBL] [Abstract][Full Text] [Related]
10. Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing? Kenna MA; Rehm HL; Robson CD; Frangulov A; McCallum J; Yaeger D; Krantz ID Am J Med Genet A; 2007 Jul; 143A(14):1560-6. PubMed ID: 17455295 [TBL] [Abstract][Full Text] [Related]
11. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families. Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379 [TBL] [Abstract][Full Text] [Related]
12. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574 [TBL] [Abstract][Full Text] [Related]
13. Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria. Janecke AR; Hirst-Stadlmann A; Günther B; Utermann B; Müller T; Löffler J; Utermann G; Nekahm-Heis D Hum Genet; 2002 Aug; 111(2):145-53. PubMed ID: 12189487 [TBL] [Abstract][Full Text] [Related]
14. [Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]. Wang G; Yuan Y; Li R; Han M; Huang S; Kang D; Zhang X; Dong M; Dai P; Han D Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 May; 25(10):445-8. PubMed ID: 21809555 [TBL] [Abstract][Full Text] [Related]
15. [The study on 235delC mutation of GJB2 gene in patients with idiopathic sudden hearing loss]. Zhan Y; Hu Y; Huang X; Chen H; Guo C; Xiao H; Shi H; Kong W Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2014 May; 28(9):621-3, 634. PubMed ID: 25195268 [TBL] [Abstract][Full Text] [Related]
16. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates. Hochman JB; Stockley TL; Shipp D; Lin VY; Chen JM; Nedzelski JM Otol Neurotol; 2010 Aug; 31(6):919-22. PubMed ID: 20601923 [TBL] [Abstract][Full Text] [Related]
17. Clinical course of hearing and language development in GJB2 and non-GJB2 deafness following habilitation with hearing aids. Matsunaga T; Hirota E; Bito S; Niimi S; Usami S Audiol Neurootol; 2006; 11(1):59-68. PubMed ID: 16282682 [TBL] [Abstract][Full Text] [Related]
18. Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese family. Huang A; Yuan Y; Duan N; Jiang X; Wang B; Liu Y; Kang D; Zhang X; Zhu Q; Dai P Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):599-603. PubMed ID: 24503448 [TBL] [Abstract][Full Text] [Related]
19. [Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)]. Barashkov NA; Dzhemileva LU; Fedorova SA; Maksimova NR; Khusnutdinova EK Vestn Otorinolaringol; 2008; (5):23-8. PubMed ID: 19008837 [TBL] [Abstract][Full Text] [Related]
20. Coincidence of mutations in different connexin genes in Hungarian patients. Tóth T; Kupka S; Haack B; Fazakas F; Muszbek L; Blin N; Pfister M; Sziklai I Int J Mol Med; 2007 Sep; 20(3):315-21. PubMed ID: 17671735 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]