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Journal Abstract Search

125 related items for PubMed ID: 36001698

  • 1. Radiologic Features in Cochlear Implant Candidates: A Prospective Study Comparing Candidates Carrying the p.Pro51Ser Mutation in Coagulation Factor C Homology With Noncarriers.
    Beerten A, Bosmans H, Lauwers M, Vermeulen H, Janssens de Varebeke SP.
    Otol Neurotol; 2022 Oct 01; 43(9):e969-e975. PubMed ID: 36001698
    [Abstract] [Full Text] [Related]

  • 2. Focal sclerosis of semicircular canals with severe DFNA9 hearing impairment caused by a P51S COCH-mutation: is there a link?
    de Varebeke SP, Termote B, Van Camp G, Govaerts PJ, Schepers S, Cox T, Deben K, Ketelslagers K, Souverijns G.
    Otol Neurotol; 2014 Jul 01; 35(6):1077-86. PubMed ID: 24662630
    [Abstract] [Full Text] [Related]

  • 3. Genotype-Phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9) Part II: A Prospective Cross-Sectional Study of the Vestibular Phenotype in 111 Carriers.
    JanssensdeVarebeke SPF, Moyaert J, Fransen E, Bulen B, Neesen C, Devroye K, van de Berg R, Pennings RJE, Topsakal V, Vanderveken O, Van Camp G, Van Rompaey V.
    Ear Hear; 2014 Jul 01; 42(6):1525-1543. PubMed ID: 34369417
    [Abstract] [Full Text] [Related]

  • 4. Genotype-phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9): Part I-A Cross-sectional Study of Hearing Function in 111 Carriers.
    JanssensdeVarebeke SPF, Moyaert J, Fransen E, Bulen B, Neesen C, Devroye K, van de Berg R, Pennings RJE, Topsakal V, Vanderveken O, Van Camp G, Van Rompaey V.
    Ear Hear; 2014 Jul 01; 42(6):1508-1524. PubMed ID: 34369416
    [Abstract] [Full Text] [Related]

  • 5. Does Vestibulo-Ocular Reflex (VOR) Gain Correlate With Radiological Findings in the Semi-Circular Canals in Patients Carrying the p.Pro51Ser (P51S) COCH Variant Causing DFNA9? Relationship Between the Three-Dimensional Video Head Impulse Test (vHIT) and MR/CT Imaging.
    Salah M, Moyaert J, Vanderveken O, Schepers S, Termote B, Van Rompaey V, Janssens de Varebeke S.
    Otol Neurotol; 2022 Mar 01; 43(3):e348-e354. PubMed ID: 35020687
    [Abstract] [Full Text] [Related]

  • 6. A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene.
    JanssensdeVarebeke S, Topsakal V, Van Camp G, Van Rompaey V.
    Eur Arch Otorhinolaryngol; 2019 May 01; 276(5):1251-1262. PubMed ID: 30806805
    [Abstract] [Full Text] [Related]

  • 7. Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutation.
    Kemperman MH, De Leenheer EM, Huygen PL, van Duijnhoven G, Morton CC, Robertson NG, Cremers FP, Kremer H, Cremers CW.
    Otol Neurotol; 2005 Sep 01; 26(5):926-33. PubMed ID: 16151339
    [Abstract] [Full Text] [Related]

  • 8. Correlations Between Vestibular Function and Imaging of the Semicircular Canals in DFNA9 Patients.
    Ihtijarevic B, Janssens de Varebeke S, Mertens G, Dekeyzer S, Van de Heyning P, Van Rompaey V.
    Front Neurol; 2019 Sep 01; 10():1341. PubMed ID: 31998212
    [Abstract] [Full Text] [Related]

  • 9. Prevalence of Endolymphatic Hydrops in Cochlear Implant Candidates with Idiopathic Profound Sensorineural Hearing Loss.
    Mosimann E, Bächinger D, Eckhard A, Reddiess P, Veraguth D, Röösli C, Huber A, De Vere-Tyndall A, Winklhofer S, Dlugaiczyk J, Dalbert A.
    Otol Neurotol; 2022 Oct 01; 43(9):e984-e991. PubMed ID: 36006776
    [Abstract] [Full Text] [Related]

  • 10. Distinct vestibular phenotypes in DFNA9 families with COCH variants.
    Kim BJ, Kim AR, Han KH, Rah YC, Hyun J, Ra BS, Koo JW, Choi BY.
    Eur Arch Otorhinolaryngol; 2016 Oct 01; 273(10):2993-3002. PubMed ID: 26758463
    [Abstract] [Full Text] [Related]

  • 11. Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W.
    Pauw RJ, Collin RW, Huygen PL, Hoefsloot LH, Kremer H, Cremers CW.
    Audiol Neurootol; 2007 Oct 01; 12(2):77-84. PubMed ID: 17264471
    [Abstract] [Full Text] [Related]

  • 12. Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers.
    Bischoff AM, Huygen PL, Kemperman MH, Pennings RJ, Bom SJ, Verhagen WI, Admiraal RJ, Kremer H, Cremers CW.
    Otol Neurotol; 2005 Sep 01; 26(5):918-25. PubMed ID: 16151338
    [Abstract] [Full Text] [Related]

  • 13. How does cochlear implantation affect five vestibular end-organ functions and dizziness?
    Dagkiran M, Tuncer U, Surmelioglu O, Tarkan O, Ozdemir S, Cetik F, Kiroglu M.
    Auris Nasus Larynx; 2019 Apr 01; 46(2):178-185. PubMed ID: 30100248
    [Abstract] [Full Text] [Related]

  • 14. Accelerated Cognitive Decline Associated With Hearing Loss and Bilateral Vestibulopathy: Insights From a Prospective Cross-Sectional Study Using the Repeatable Battery for the Assessment of Neuropsychological Status Adjusted for the Hearing Impaired in the DFNA9 Population.
    Gommeren H, Bosmans J, Moyaert J, Mertens G, Cras P, Engelborghs S, Van Ombergen A, Gilles A, Fransen E, van de Berg R, JanssensdeVarebeke S, Van Rompaey V.
    Ear Hear; 2019 Apr 01; 44(4):697-709. PubMed ID: 36607747
    [Abstract] [Full Text] [Related]

  • 15. Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene.
    Verstreken M, Declau F, Wuyts FL, D'Haese P, Van Camp G, Fransen E, Van den Hauwe L, Buyle S, Smets RE, Feenstra L, Van der Stappen A, Van de Heyning PH.
    Otol Neurotol; 2001 Nov 01; 22(6):874-81. PubMed ID: 11698812
    [Abstract] [Full Text] [Related]

  • 16. Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo (DFNA9/COCH): longitudinal analyses in a belgian family.
    Lemaire FX, Feenstra L, Huygen PL, Fransen E, Devriendt K, Van Camp G, Vantrappen G, Cremers CW, Wackym PA, Koss JC.
    Otol Neurotol; 2003 Sep 01; 24(5):743-8. PubMed ID: 14501450
    [Abstract] [Full Text] [Related]

  • 17. Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion.
    Jung J, Kim HS, Lee MG, Yang EJ, Choi JY.
    Hum Mutat; 2015 Dec 01; 36(12):1168-75. PubMed ID: 26256111
    [Abstract] [Full Text] [Related]

  • 18. Phenotype description of a novel DFNA9/COCH mutation, I109T.
    Pauw RJ, Huygen PL, Collin RW, Cruysberg JR, Hoefsloot LH, Kremer H, Cremers CW.
    Ann Otol Rhinol Laryngol; 2007 May 01; 116(5):349-57. PubMed ID: 17561763
    [Abstract] [Full Text] [Related]

  • 19. Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder.
    Jones SM, Robertson NG, Given S, Giersch AB, Liberman MC, Morton CC.
    Hear Res; 2011 Feb 01; 272(1-2):42-8. PubMed ID: 21073934
    [Abstract] [Full Text] [Related]

  • 20. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.
    Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, Kuo SF, Liberman MC, Merchant SN, Miller CE, Nadol JB, Sarracino DA, Verhagen WI, Morton CC.
    Hum Mol Genet; 2006 Apr 01; 15(7):1071-85. PubMed ID: 16481359
    [Abstract] [Full Text] [Related]

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