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PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 21436747

  • 1.
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  • 2. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug; 27(5):681-6. PubMed ID: 16868516
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  • 5. 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; 125(9):2175-80. PubMed ID: 25946228
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  • 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; 11(10):744-8. PubMed ID: 14512963
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  • 7. Inheritance of Meniere's disease in the Finnish population.
    Klockars T, Kentala E.
    Arch Otolaryngol Head Neck Surg; 2007 Jan; 133(1):73-7. PubMed ID: 17224529
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  • 9. A Meniere's disease gene linked to chromosome 12p12.3.
    Klar J, Frykholm C, Friberg U, Dahl N.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Jul 05; 141B(5):463-7. PubMed ID: 16741942
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  • 11. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.
    Arch Neurol; 2006 Nov 05; 63(11):1591-8. PubMed ID: 17101828
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  • 12. Prevalence of Menière's disease in general population of Southern Finland.
    Havia M, Kentala E, Pyykkö I.
    Otolaryngol Head Neck Surg; 2005 Nov 05; 133(5):762-8. PubMed ID: 16274806
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  • 13. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE, Ritch R, Lichter PR, Rozsa FW, Stringham HM, Caronia RM, Johnson D, Abundo GP, Willcockson J, Downs CA, Thompson DA, Musarella MA, Gupta N, Othman MI, Torrez DM, Herman SB, Wong DJ, Higashi M, Boehnke M.
    Ophthalmology; 1998 Sep 05; 105(9):1698-707. PubMed ID: 9754180
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  • 14. Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26.
    Klein KM, Bromhead CJ, Smith KR, O'Callaghan CJ, Corcoran SJ, Heron SE, Iona X, Hodgson BL, McMahon JM, Lawrence KM, Scheffer IE, Dibbens LM, Bahlo M, Berkovic SF.
    Neurology; 2013 Apr 16; 80(16):1485-93. PubMed ID: 23589636
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  • 15. Transtympanic steroids for Ménière's disease.
    Herraiz C, Plaza G, Aparicio JM, Gallego I, Marcos S, Ruiz C.
    Otol Neurotol; 2010 Jan 16; 31(1):162-7. PubMed ID: 19924013
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  • 16. [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 16; 50(11):915-24. PubMed ID: 26887996
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  • 17. Higher prevalence of autoimmune diseases and longer spells of vertigo in patients affected with familial Ménière's disease: A clinical comparison of familial and sporadic Ménière's disease.
    Hietikko E, Sorri M, Männikkö M, Kotimäki J.
    Am J Audiol; 2014 Jun 16; 23(2):232-7. PubMed ID: 24686733
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