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Journal Abstract Search

233 related items for PubMed ID: 26887996

  • 1. [Cinical and genetic characteristics of familial Meniere's disease: three families report].
    Gao Y, Wang D, Wang H, Guan J, Lan L, Wu Z, Xie L, Yu L, Zhang S, Shan X, Wang Q.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 50(11):915-24. PubMed ID: 26887996
    [Abstract] [Full Text] [Related]

  • 2. Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.
    Mehrjoo Z, Kahrizi K, Mohseni M, Akbari M, Arzhangi S, Jalalvand K, Najmabadi H, Farhadi M, Mohseni M, Asghari A, Mohebbi S, Daneshi A.
    Arch Iran Med; 2020 May 01; 23(5):319-325. PubMed ID: 32383616
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Ménière's disease in children aged 4-7 years.
    Brantberg K, Duan M, Falahat B.
    Acta Otolaryngol; 2012 May 01; 132(5):505-9. PubMed ID: 22217217
    [Abstract] [Full Text] [Related]

  • 5. Analysis of Saccular Function With Vestibular Evoked Myogenic Potential Test in Meniere's Disease.
    Dabiri S, Yazdani N, Esfahani M, Tari N, Adil S, Mahvi Z, Rezazadeh N.
    Acta Med Iran; 2017 Feb 01; 55(2):123-127. PubMed ID: 28282709
    [Abstract] [Full Text] [Related]

  • 6. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
    Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.
    Eur J Hum Genet; 2003 Oct 01; 11(10):744-8. PubMed ID: 14512963
    [Abstract] [Full Text] [Related]

  • 7. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug 01; 27(5):681-6. PubMed ID: 16868516
    [Abstract] [Full Text] [Related]

  • 8. Genetic aspects and clinical characteristics of familial Meniere's disease in a South Korean population.
    Lee JM, Kim MJ, Jung J, Kim HJ, Seo YJ, Kim SH.
    Laryngoscope; 2015 Sep 01; 125(9):2175-80. PubMed ID: 25946228
    [Abstract] [Full Text] [Related]

  • 9. A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.
    Martín-Sierra C, Requena T, Frejo L, Price SD, Gallego-Martinez A, Batuecas-Caletrio A, Santos-Pérez S, Soto-Varela A, Lysakowski A, Lopez-Escamez JA.
    Hum Mol Genet; 2016 Aug 15; 25(16):3407-3415. PubMed ID: 27329761
    [Abstract] [Full Text] [Related]

  • 10. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.
    Fransen E, Verstreken M, Verhagen WI, Wuyts FL, Huygen PL, D'Haese P, Robertson NG, Morton CC, McGuirt WT, Smith RJ, Declau F, Van de Heyning PH, Van Camp G.
    Hum Mol Genet; 1999 Aug 15; 8(8):1425-9. PubMed ID: 10400989
    [Abstract] [Full Text] [Related]

  • 11. Ménière's disease is a disorder of the inner ear.
    Ahmad JG, Lin KF.
    Curr Opin Otolaryngol Head Neck Surg; 2023 Oct 01; 31(5):320-324. PubMed ID: 37610986
    [Abstract] [Full Text] [Related]

  • 12. Initial symptoms and retrospective evaluation of prognosis in Menière's disease.
    Tokumasu K, Fujino A, Naganuma H, Hoshino I, Arai M.
    Acta Otolaryngol Suppl; 1996 Oct 01; 524():43-9. PubMed ID: 8790762
    [Abstract] [Full Text] [Related]

  • 13. Familial clustering of migraine, episodic vertigo, and Ménière's disease.
    Cha YH, Kane MJ, Baloh RW.
    Otol Neurotol; 2008 Jan 01; 29(1):93-6. PubMed ID: 18046258
    [Abstract] [Full Text] [Related]

  • 14. ENG in a patient with Ménière's syndrome and evidence of vestibular recruitment.
    Brookler KH.
    Ear Nose Throat J; 2003 Nov 01; 82(11):846-8. PubMed ID: 14661433
    [No Abstract] [Full Text] [Related]

  • 15. A unified hypothesis for vestibular dysfunction?
    Phillips JS, Prinsley PR.
    Otolaryngol Head Neck Surg; 2009 Apr 01; 140(4):477-9. PubMed ID: 19328333
    [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. RotaRod and acoustic startle reflex performance of two potential mouse models for Meniere's disease.
    Babu V, Bahari R, Laban N, Kulaga J, Abdul Z, Zakkar B, Al-Najjar A, Lesus J, Al-Rifai AA, Sattar H, Irukulla S, Gunniya P, Requena T, Lysakowski A.
    Eur J Neurosci; 2023 Aug 01; 58(3):2708-2723. PubMed ID: 37461313
    [Abstract] [Full Text] [Related]

  • 18. [Simultaneous triple semicircular canal plugging and cochlear implantation in advanced Meniere's disease].
    Zhang DG, Xu L, Han YC, Lyu YF, Luo JF, Li YW, Wang RJ, Fan ZM, Wang HB.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Jan 07; 52(1):25-30. PubMed ID: 28104012
    [Abstract] [Full Text] [Related]

  • 19. [Diagnosis and outcome analysis of diseases characterized by recurrent low-frequency sensorineural deafness].
    Wu K, Wang D, Wang H, Wang H, Guan J, Zhao L, Wang Q.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2020 Feb 07; 34(2):106-112. PubMed ID: 32086912
    [Abstract] [Full Text] [Related]

  • 20. [Caloric test and hearing characteristics in patients with vestibular migraine and Meniere's disease].
    Yu X, Wang LY, Han W, Tian LJ, Liu XL.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Mar 07; 33(3):228-231. PubMed ID: 30813691
    [Abstract] [Full Text] [Related]

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