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Journal Abstract Search

180 related items for PubMed ID: 11527035

  • 1. Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss.
    Elfenbein JL, Fisher RA, Wei S, Morell RJ, Stewart C, Friedman TB, Friderici K.
    Ear Hear; 2001 Aug; 22(4):279-88. PubMed ID: 11527035
    [Abstract] [Full Text] [Related]

  • 2. Audiologic evidence for further genetic heterogeneity at DFNA2.
    Stern RE, Lalwani AK.
    Acta Otolaryngol; 2002 Oct; 122(7):730-5. PubMed ID: 12484650
    [Abstract] [Full Text] [Related]

  • 3. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
    [Abstract] [Full Text] [Related]

  • 4. A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
    Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE.
    Am J Otol; 1998 Nov; 19(6):718-23. PubMed ID: 9831143
    [Abstract] [Full Text] [Related]

  • 5. The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.
    Kunst H, Huybrechts C, Marres H, Huygen P, Van Camp G, Cremers C.
    Am J Otol; 2000 Mar; 21(2):181-7. PubMed ID: 10733181
    [Abstract] [Full Text] [Related]

  • 6. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss].
    Ni D, Dan H, Mo J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr; 34(2):77-80. PubMed ID: 12764852
    [Abstract] [Full Text] [Related]

  • 7. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
    [Abstract] [Full Text] [Related]

  • 8. Audiologic Manifestations of Marshall Syndrome.
    Bacciu A, Di Lella F, Iaccarino I, Pasanisi E, Fava G, Vincenti V, Falcioni M.
    Otol Neurotol; 2018 Sep; 39(8):e691-e698. PubMed ID: 30020262
    [Abstract] [Full Text] [Related]

  • 9. Confirmation of PDZD7 as a Nonsyndromic Hearing Loss Gene.
    Vona B, Lechno S, Hofrichter MA, Hopf S, Läig AK, Haaf T, Keilmann A, Zechner U, Bartsch O.
    Ear Hear; 2016 Sep; 37(4):e238-46. PubMed ID: 26849169
    [Abstract] [Full Text] [Related]

  • 10. Association of TMTC2 With Human Nonsyndromic Sensorineural Hearing Loss.
    Runge CL, Indap A, Zhou Y, Kent JW, King E, Erbe CB, Cole R, Littrell J, Merath K, James R, Rüschendorf F, Kerschner JE, Marth G, Hübner N, Göring HH, Friedland DR, Kwok WM, Olivier M.
    JAMA Otolaryngol Head Neck Surg; 2016 Sep 01; 142(9):866-72. PubMed ID: 27311106
    [Abstract] [Full Text] [Related]

  • 11. Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.
    Makishima T, Kurima K, Brewer CC, Griffith AJ.
    Otol Neurotol; 2004 Sep 01; 25(5):714-9. PubMed ID: 15354000
    [Abstract] [Full Text] [Related]

  • 12. Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.
    Arnett J, Emery SB, Kim TB, Boerst AK, Lee K, Leal SM, Lesperance MM.
    Arch Otolaryngol Head Neck Surg; 2011 Jan 01; 137(1):54-9. PubMed ID: 21242547
    [Abstract] [Full Text] [Related]

  • 13. [Measuring and analyzing of otoacoustic emission tests of a family with genetic progressive sensorineural hearing loss].
    Yu H, Ke XM, Yu DL, Li Q, Liu YH, Ding GY.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2000 Apr 01; 14(4):157-9. PubMed ID: 12541488
    [Abstract] [Full Text] [Related]

  • 14. Audiological and radiological characteristics of a family with T961G mitochondrial mutation.
    Turchetta R, Mazzei F, Celani T, Cammeresi MG, Orlando MP, Altissimi G, de Vincentiis C, D'Ambrosio F, Messineo D, Ferraris A, Cianfrone G.
    Int J Audiol; 2012 Dec 01; 51(12):870-9. PubMed ID: 23013294
    [Abstract] [Full Text] [Related]

  • 15. A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.
    Kemperman MH, De Leenheer EM, Huygen PL, van Wijk E, van Duijnhoven G, Cremers FP, Kremer H, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 2004 Mar 01; 130(3):281-8. PubMed ID: 15023833
    [Abstract] [Full Text] [Related]

  • 16. A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration.
    Lalwani AK, Linthicum FH, Wilcox ER, Moore JK, Walters FC, San Agustin TB, Mislinski J, Miller MR, Sinninger Y, Attaie A, Luxford WM.
    Audiol Neurootol; 1997 Mar 01; 2(3):139-54. PubMed ID: 9390828
    [Abstract] [Full Text] [Related]

  • 17. A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.
    Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA.
    Genomics; 2000 Jan 01; 63(1):1-6. PubMed ID: 10662538
    [Abstract] [Full Text] [Related]

  • 18. AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance.
    Lang-Roth R, Fischer-Krall E, Kornblum C, Nürnberg G, Meschede D, Goebel I, Nürnberg P, Beutner D, Kubisch C, Walger M, Volk AE.
    Audiol Neurootol; 2017 Jan 01; 22(1):30-40. PubMed ID: 28601886
    [Abstract] [Full Text] [Related]

  • 19. Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).
    Zhu M, Yang T, Wei S, DeWan AT, Morell RJ, Elfenbein JL, Fisher RA, Leal SM, Smith RJ, Friderici KH.
    Am J Hum Genet; 2003 Nov 01; 73(5):1082-91. PubMed ID: 13680526
    [Abstract] [Full Text] [Related]

  • 20. Phenotypic characterization of DFNA24: prelingual progressive sensorineural hearing impairment.
    Santos RL, Häfner FM, Huygen PL, Linder TE, Schinzel AA, Spillmann T, Leal SM.
    Audiol Neurootol; 2006 Nov 01; 11(5):269-75. PubMed ID: 16717440
    [Abstract] [Full Text] [Related]

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