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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 12527132

  • 1. Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.
    Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, Saleh B, Pratt H.
    Hear Res; 2003 Jan; 175(1-2):140-51. PubMed ID: 12527132
    [Abstract] [Full Text] [Related]

  • 2. The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers.
    Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, Barges S, Pratt H.
    Hear Res; 2002 Jan; 163(1-2):93-100. PubMed ID: 11788203
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene.
    Santarelli R, Del Castillo I, Rodríguez-Ballesteros M, Scimemi P, Cama E, Arslan E, Starr A.
    J Assoc Res Otolaryngol; 2009 Dec; 10(4):545-56. PubMed ID: 19636622
    [Abstract] [Full Text] [Related]

  • 5. 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. PubMed ID: 15064611
    [Abstract] [Full Text] [Related]

  • 6. Hearing function in heterozygous carriers of a pathogenic GJB2 gene mutation.
    Groh D, Seeman P, Jilek M, Popelář J, Kabelka Z, Syka J.
    Physiol Res; 2013 Apr; 62(3):323-30. PubMed ID: 23489192
    [Abstract] [Full Text] [Related]

  • 7. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).
    Cohn ES, Kelley PM, Fowler TW, Gorga MP, Lefkowitz DM, Kuehn HJ, Schaefer GB, Gobar LS, Hahn FJ, Harris DJ, Kimberling WJ.
    Pediatrics; 1999 Mar; 103(3):546-50. PubMed ID: 10049954
    [Abstract] [Full Text] [Related]

  • 8. Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf.
    Cheng X, Li L, Brashears S, Morlet T, Ng SS, Berlin C, Hood L, Keats B.
    Am J Med Genet A; 2005 Nov 15; 139(1):13-8. PubMed ID: 16222667
    [Abstract] [Full Text] [Related]

  • 9. [Effect of inner ear hearing loss on delayed otoacoustic emissions (TEOAE) and distortion products (DPOAE)].
    Hoth S.
    Laryngorhinootologie; 1996 Dec 15; 75(12):709-18. PubMed ID: 9081275
    [Abstract] [Full Text] [Related]

  • 10. A novel connexin 26 compound heterozygous mutation results in deafness.
    Harris KC, Erbe CB, Firszt JB, Flanary VA, Wackym PA.
    Laryngoscope; 2002 Jul 15; 112(7 Pt 1):1159-62. PubMed ID: 12169891
    [Abstract] [Full Text] [Related]

  • 11. Temporal bone histopathology in connexin 26-related hearing loss.
    Jun AI, McGuirt WT, Hinojosa R, Green GE, Fischel-Ghodsian N, Smith RJ.
    Laryngoscope; 2000 Feb 15; 110(2 Pt 1):269-75. PubMed ID: 10680928
    [Abstract] [Full Text] [Related]

  • 12. Differential effects of salicylate, quinine, and furosemide on Guinea pig inner and outer hair cell function revealed by the input-output relation of the auditory brainstem response.
    Pienkowski M, Ulfendahl M.
    J Am Acad Audiol; 2011 Feb 15; 22(2):104-12. PubMed ID: 21463565
    [Abstract] [Full Text] [Related]

  • 13. [Otoacoustic emissions, auditory evoked potentials, pure tone thresholds and speech intelligibility in cases of auditory neuropathy].
    Ptok M.
    HNO; 2000 Jan 15; 48(1):28-32. PubMed ID: 10663046
    [Abstract] [Full Text] [Related]

  • 14. Otoacoustic emissions--an approach for monitoring aminoglycoside induced ototoxicity in children.
    Stavroulaki P, Apostolopoulos N, Dinopoulou D, Vossinakis I, Tsakanikos M, Douniadakis D.
    Int J Pediatr Otorhinolaryngol; 1999 Nov 05; 50(3):177-84. PubMed ID: 10595663
    [Abstract] [Full Text] [Related]

  • 15. Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds.
    Kitao K, Mutai H, Namba K, Morimoto N, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Okamoto Y, Morita N, Sakamoto H, Shintani T, Fukuda S, Kaga K, Matsunaga T.
    Ear Hear; 2019 Nov 05; 40(1):184-191. PubMed ID: 29688962
    [Abstract] [Full Text] [Related]

  • 16. 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 05; 27(6):732-41. PubMed ID: 17086082
    [Abstract] [Full Text] [Related]

  • 17. Audiological features of GJB2 (connexin 26) deafness.
    Liu XZ, Pandya A, Angeli S, Telischi FF, Arnos KS, Nance WE, Balkany T.
    Ear Hear; 2005 Jun 05; 26(3):361-9. PubMed ID: 15937416
    [Abstract] [Full Text] [Related]

  • 18. Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.
    Mesolella M, Tranchino G, Nardone M, Motta S, Galli V.
    Int J Pediatr Otorhinolaryngol; 2004 Aug 05; 68(8):995-1005. PubMed ID: 15236885
    [Abstract] [Full Text] [Related]

  • 19. Distortion product otoacoustic emissions and outer hair cell defects in the hyt/hyt mutant mouse.
    Li D, Henley CM, O'Malley BW.
    Hear Res; 1999 Dec 05; 138(1-2):65-72. PubMed ID: 10575115
    [Abstract] [Full Text] [Related]

  • 20. Cx26 deafness: mutation analysis and clinical variability.
    Murgia A, Orzan E, Polli R, Martella M, Vinanzi C, Leonardi E, Arslan E, Zacchello F.
    J Med Genet; 1999 Nov 05; 36(11):829-32. PubMed ID: 10544226
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.