These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 16469394)

  • 1. Late postnatal onset of hearing loss due to GJB2 mutations.
    Pagarkar W; Bitner-Glindzicz M; Knight J; Sirimanna T
    Int J Pediatr Otorhinolaryngol; 2006 Jun; 70(6):1119-24. PubMed ID: 16469394
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort.
    Cama E; Melchionda S; Palladino T; Carella M; Santarelli R; Genovese E; Benettazzo F; Zelante L; Arslan E
    Int J Audiol; 2009 Jan; 48(1):12-7. PubMed ID: 19173109
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Hearing loss associated with 35delG mutation in Connexin-26 (GJB2) gene: audiogram analysis.
    Salvinelli F; Casale M; D'Ascanio L; Firrisi L; Greco F; Baldi A
    J Laryngol Otol; 2004 Jan; 118(1):8-11. PubMed ID: 14979964
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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. PubMed ID: 17086082
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening].
    Prera N; Löhle E; Birkenhäger R
    Laryngorhinootologie; 2014 Apr; 93(4):244-8. PubMed ID: 24022696
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Is hearing loss due to mutations in the Connexin 26 gene progressive?
    Gopalarao D; Kimberling WJ; Jesteadt W; Kelley PM; Beauchaine KL; Cohn ES
    Int J Audiol; 2008 Jan; 47(1):11-20. PubMed ID: 18196482
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cx26 gene mutations in idiopathic progressive hearing loss.
    Ravecca F; Berrettini S; Forli F; Marcaccini M; Casani A; Baldinotti F; Fogli A; Siciliano G; Simi P
    J Otolaryngol; 2005 Apr; 34(2):126-34. PubMed ID: 16076412
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GJB2 mutations and additional disabilities in a pediatric cochlear implant population.
    Wiley S; Choo D; Meinzen-Derr J; Hilbert L; Greinwald J
    Int J Pediatr Otorhinolaryngol; 2006 Mar; 70(3):493-500. PubMed ID: 16154643
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [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]  

  • 13. Prevalence of mutations located at the dfnb1 locus in a population of cochlear implanted children in eastern Romania.
    Rădulescu L; Mârţu C; Birkenhäger R; Cozma S; Ungureanu L; Laszig R
    Int J Pediatr Otorhinolaryngol; 2012 Jan; 76(1):90-4. PubMed ID: 22070872
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene.
    Tekin M; Duman T; Boğoçlu G; Incesulu A; Cin S; Akar N
    Genet Couns; 2003; 14(4):379-86. PubMed ID: 14738110
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.
    Teek R; Kruustük K; Zordania R; Joost K; Reimand T; Möls T; Oitmaa E; Kahre T; Tõnisson N; Ounap K
    Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1007-12. PubMed ID: 20708129
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
    Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L
    Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.
    Riahi Z; Zainine R; Mellouli Y; Hannachi R; Bouyacoub Y; Laroussi N; Beltaief N; Kefi R; Romdhane L; Bonnet C; Abdelhak S; Besbes G
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1481-4. PubMed ID: 23856378
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of GJB2 gene mutation with cochlear implant performance in genetic non-syndromic hearing loss.
    Karamert R; Bayazit YA; Altinyay S; Yılmaz A; Menevse A; Gokdogan O; Gokdogan C; Ant A
    Int J Pediatr Otorhinolaryngol; 2011 Dec; 75(12):1572-5. PubMed ID: 21996152
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions.
    Santarelli R; Cama E; Scimemi P; Dal Monte E; Genovese E; Arslan E
    Eur Arch Otorhinolaryngol; 2008 Jan; 265(1):43-51. PubMed ID: 17701047
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.