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Journal Abstract Search

102 related items for PubMed ID: 20927121

  • 1. Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association.
    Gabriková D, Frykholm C, Friberg U, Lahsaee S, Entesarian M, Dahl N, Klar J.
    J Hum Genet; 2010 Dec; 55(12):834-7. PubMed ID: 20927121
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Genetic aspects of familial Ménière's disease.
    Arweiler-Harbeck D, Horsthemke B, Jahnke K, Hennies HC.
    Otol Neurotol; 2011 Jun 05; 32(4):695-700. PubMed ID: 21436747
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  • 4. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug 05; 27(5):681-6. PubMed ID: 16868516
    [Abstract] [Full Text] [Related]

  • 5. On genetic and environmental factors in Menière's disease.
    Morrison AW, Mowbray JF, Williamson R, Sheeka S, Sodha N, Koskinen N.
    Am J Otol; 1994 Jan 05; 15(1):35-9. PubMed ID: 8109627
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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 05; 11(10):744-8. PubMed ID: 14512963
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  • 7. 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 05; 125(9):2175-80. PubMed ID: 25946228
    [Abstract] [Full Text] [Related]

  • 8. Inheritance of Meniere's disease in the Finnish population.
    Klockars T, Kentala E.
    Arch Otolaryngol Head Neck Surg; 2007 Jan 05; 133(1):73-7. PubMed ID: 17224529
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  • 10. Familial Menière's disease: a genetic investigation.
    Birgerson L, Gustavson KH, Stahle J.
    Am J Otol; 1987 Jul 05; 8(4):323-6. PubMed ID: 3631240
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  • 11. Association of familial and sporadic rheumatoid arthritis with a single corticotropin-releasing hormone genomic region (8q12.3) haplotype.
    Fife M, Steer S, Fisher S, Newton J, McKay K, Worthington J, Shah C, Polley A, Rosenthal A, Ollier W, Lewis C, Wordsworth P, Lanchbury J.
    Arthritis Rheum; 2002 Jan 05; 46(1):75-82. PubMed ID: 11817611
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  • 12. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 05; 152(1):29-36. PubMed ID: 15656797
    [Abstract] [Full Text] [Related]

  • 13. 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 05; 8(8):1425-9. PubMed ID: 10400989
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  • 16. Familial clustering and genetic heterogeneity in Meniere's disease.
    Requena T, Espinosa-Sanchez JM, Cabrera S, Trinidad G, Soto-Varela A, Santos-Perez S, Teggi R, Perez P, Batuecas-Caletrio A, Fraile J, Aran I, Martin E, Benitez J, Pérez-Fernández N, Lopez-Escamez JA.
    Clin Genet; 2014 Mar 05; 85(3):245-52. PubMed ID: 23521103
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  • 17. Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.
    Hadj-Rabia S, Salomon R, Pelet A, Penet C, Rotschild A, de Laët MH, Chaouachi B, Hannachi R, Bakiri F, Brauner R, Chaussain JL, Munnich A, Lyonnet S.
    Eur J Hum Genet; 2000 Aug 05; 8(8):613-20. PubMed ID: 10951524
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  • 18. Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.
    Furuta T, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sugiura M, Sone M, Hiramatsu M, Sugiura S, Ando F, Shimokata H, Nakashima T.
    Int J Immunogenet; 2011 Jun 05; 38(3):249-54. PubMed ID: 21385326
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  • 20. Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease.
    Escalera-Balsera A, Roman-Naranjo P, Lopez-Escamez JA.
    Genes (Basel); 2020 Nov 27; 11(12):. PubMed ID: 33260921
    [Abstract] [Full Text] [Related]

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