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Volumn 11, Issue 12, 2012, Pages 925-926

Genetic and clinical heterogeneity in Meniere's disease

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN G; IMMUNOGLOBULIN G ANTIBODY;

EID: 84866532009     PISSN: 15689972     EISSN: 18730183     Source Type: Journal    
DOI: 10.1016/j.autrev.2012.02.020     Document Type: Letter
Times cited : (7)

References (11)
  • 1
    • 78650564914 scopus 로고    scopus 로고
    • Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association
    • Grabrikova D., Frykholm C., Friberg U., Lahsaee S., Entesarian M., Dahl N., et al. Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association. J Hum Genet 2010, 55(12):834-837.
    • (2010) J Hum Genet , vol.55 , Issue.12 , pp. 834-837
    • Grabrikova, D.1    Frykholm, C.2    Friberg, U.3    Lahsaee, S.4    Entesarian, M.5    Dahl, N.6
  • 3
    • 79955897567 scopus 로고    scopus 로고
    • Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings
    • Hietikko E., Kotimaki J., Kentala E., Klockars T., Sorri M., Mannikko M. Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings. Genet Med 2011, 13(5):415-420.
    • (2011) Genet Med , vol.13 , Issue.5 , pp. 415-420
    • Hietikko, E.1    Kotimaki, J.2    Kentala, E.3    Klockars, T.4    Sorri, M.5    Mannikko, M.6
  • 4
    • 75149191394 scopus 로고    scopus 로고
    • Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population
    • Campbell C.A., Della Santina C.C., Meyer N.C., Smith N.B., Myrie O.A., Stone E.M., et al. Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population. Am J Med Genet A 2010, 152A:67-74.
    • (2010) Am J Med Genet A , vol.152 A , pp. 67-74
    • Campbell, C.A.1    Della Santina, C.C.2    Meyer, N.C.3    Smith, N.B.4    Myrie, O.A.5    Stone, E.M.6
  • 5
    • 80052844037 scopus 로고    scopus 로고
    • Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Menière's disease in a European Caucasian population
    • Gazquez I., Lopez-Escamez J.A., Moreno A., Campbell C.A., Meyer N.C., Carey J.P., et al. Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Menière's disease in a European Caucasian population. DNA Cell Biol 2011, 30(9):699-708.
    • (2011) DNA Cell Biol , vol.30 , Issue.9 , pp. 699-708
    • Gazquez, I.1    Lopez-Escamez, J.A.2    Moreno, A.3    Campbell, C.A.4    Meyer, N.C.5    Carey, J.P.6
  • 6
    • 80052854166 scopus 로고    scopus 로고
    • Genetics of recurrent vertigo and vestibular disorders
    • Gazquez I., Lopez-Escamez J.A. Genetics of recurrent vertigo and vestibular disorders. Curr Genomics 2011, 12(6):443-450.
    • (2011) Curr Genomics , vol.12 , Issue.6 , pp. 443-450
    • Gazquez, I.1    Lopez-Escamez, J.A.2
  • 8
    • 74049157115 scopus 로고    scopus 로고
    • Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease
    • Lopez-Escamez J.A., Saenz-Lopez P., Acosta L., Moreno A., Gazquez I., Perez-Garrigues H., et al. Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease. Laryngoscope 2010, 120:103-107.
    • (2010) Laryngoscope , vol.120 , pp. 103-107
    • Lopez-Escamez, J.A.1    Saenz-Lopez, P.2    Acosta, L.3    Moreno, A.4    Gazquez, I.5    Perez-Garrigues, H.6
  • 11
    • 78650777049 scopus 로고    scopus 로고
    • Polymorphisms of CD16A and CD32 fcgamma receptors and circulating immunocomplexes in Meniere disease: a case-control study
    • Lopez-Escamez J.A., Saenz-Lopez P., Gazquez I., Moreno A., Gonzalez-Oller C., Soto-Varela A., et al. Polymorphisms of CD16A and CD32 fcgamma receptors and circulating immunocomplexes in Meniere disease: a case-control study. BMC Med Genet 2011, 12:2.
    • (2011) BMC Med Genet , vol.12 , pp. 2
    • Lopez-Escamez, J.A.1    Saenz-Lopez, P.2    Gazquez, I.3    Moreno, A.4    Gonzalez-Oller, C.5    Soto-Varela, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.