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    Results: 1 to 100 of 234

    1.

    Meniere's disease might be an autoimmune condition?

    Greco A, Gallo A, Fusconi M, Marinelli C, Macri GF, de Vincentiis M.

    Autoimmun Rev. 2012 Jan 28. [Epub ahead of print]

    PMID:
    22306860
    [PubMed - as supplied by publisher]
    2.

    [Multidisciplinary approach to the endolymphatic sac tumour].

    González-Bonet LG, Amoros-Sebastiá LI, Piquer-Belloch J, Riesgo P, Llacer JL, Gisbert-Aguilar J, Morell-Quadreny L.

    Neurocirugia (Astur). 2011 Dec;22(6):567-73. Spanish.

    PMID:
    22167288
    [PubMed - indexed for MEDLINE]
    Free Article
    3.

    Genetic disorders of the vestibular system.

    Eppsteiner RW, Smith RJ.

    Curr Opin Otolaryngol Head Neck Surg. 2011 Aug 5. [Epub ahead of print]

    PMID:
    21825995
    [PubMed - as supplied by publisher]
    4.

    Auditory and vestibular hair cell stereocilia: relationship between functionality and inner ear disease.

    Ciuman RR.

    J Laryngol Otol. 2011 Oct;125(10):991-1003. Epub 2011 Jul 21. Review.

    PMID:
    21774850
    [PubMed - indexed for MEDLINE]
    5.

    Role of genomic medicine in middle and inner ear diseases.

    López-Escamez JA.

    Acta Otorrinolaringol Esp. 2011 Jun 21. [Epub ahead of print] English, Spanish.

    PMID:
    21700264
    [PubMed - as supplied by publisher]
    Free Article
    6.

    Associations between HLA-C alleles and definite Meniere's disease.

    Khorsandi MT, Amoli MM, Borghei H, Emami H, Amiri P, Amirzargar A, Yazdani N.

    Iran J Allergy Asthma Immunol. 2011 Jun;10(2):119-22.

    PMID:
    21625020
    [PubMed - indexed for MEDLINE]
    7.

    Did Van Gogh have Ménière's disease?

    Martin C.

    Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Sep;128(4):205-9. Epub 2011 May 26.

    PMID:
    21616739
    [PubMed - indexed for MEDLINE]
    8.

    Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.

    Gazquez I, Lopez-Escamez JA, Moreno A, Campbell CA, Meyer NC, Carey JP, Minor LB, Gantz BJ, Hansen MR, Della Santina CC, Aran I, Soto-Varela A, Santos S, Batuecas A, Perez-Garrigues H, Lopez-Nevot A, Smith RJ, Lopez-Nevot MA.

    DNA Cell Biol. 2011 Sep;30(9):699-708. Epub 2011 May 25.

    PMID:
    21612410
    [PubMed - indexed for MEDLINE]
    9.

    Endolymphatic sac tumor with overexpression of V2 receptor mRNA and inner ear hydrops.

    Kitahara T, Maekawa C, Kizawa K, Kamakura T, Horii A, Inohara H.

    Acta Otolaryngol. 2011 Sep;131(9):951-7. Epub 2011 May 16.

    PMID:
    21574774
    [PubMed - indexed for MEDLINE]
    10.

    Otologic diagnoses in the elderly: current utilization and predicted workload increase.

    Lin HW, Bhattacharyya N.

    Laryngoscope. 2011 Jul;121(7):1504-7. doi: 10.1002/lary.21827. Epub 2011 May 6.

    PMID:
    21557249
    [PubMed - indexed for MEDLINE]
    11.

    [Perspectives in neurotology].

    Ernst A.

    Laryngorhinootologie. 2011 Mar;90 Suppl 1:S35-43. Epub 2011 Apr 26. Review. German.

    PMID:
    21523632
    [PubMed - indexed for MEDLINE]
    12.

    Proteomics in Ménière disease.

    Chiarella G, Saccomanno M, Scumaci D, Gaspari M, Faniello MC, Quaresima B, Di Domenico M, Ricciardi C, Petrolo C, Cassandro C, Costanzo FS, Cuda G, Cassandro E.

    J Cell Physiol. 2012 Jan;227(1):308-12. doi: 10.1002/jcp.22737.

    PMID:
    21437900
    [PubMed - indexed for MEDLINE]
    13.

    Genetic aspects of familial Ménière's disease.

    Arweiler-Harbeck D, Horsthemke B, Jahnke K, Hennies HC.

    Otol Neurotol. 2011 Jun;32(4):695-700.

    PMID:
    21436747
    [PubMed - indexed for MEDLINE]
    14.

    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;38(3):249-54. doi: 10.1111/j.1744-313X.2011.01004.x. Epub 2011 Mar 9.

    PMID:
    21385326
    [PubMed - indexed for MEDLINE]
    15.

    Genetics of vestibulopathies.

    Jen JC.

    Adv Otorhinolaryngol. 2011;70:130-4. Epub 2011 Feb 24. Review.

    PMID:
    21358195
    [PubMed - indexed for MEDLINE]
    16.

    Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings.

    Hietikko E, Kotimäki J, Kentala E, Klockars T, Sorri M, Männikkö M.

    Genet Med. 2011 May;13(5):415-20.

    PMID:
    21346584
    [PubMed - indexed for MEDLINE]
    17.

    Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study.

    Lopez-Escamez JA, Saenz-Lopez P, Gazquez I, Moreno A, Gonzalez-Oller C, Soto-Varela A, Santos S, Aran I, Perez-Garrigues H, Ibañez A, Lopez-Nevot MA.

    BMC Med Genet. 2011 Jan 5;12:2.

    PMID:
    21208440
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    18.

    Transport augmentation through the blood-inner ear barriers of guinea pigs treated with 3-nitropropionic acid and patients with acute hearing loss, visualized with 3.0 T MRI.

    Zou J, Li M, Zhang Y, Zheng G, Chen D, Chen S, Zheng H.

    Otol Neurotol. 2011 Feb;32(2):204-12.

    PMID:
    21150687
    [PubMed - indexed for MEDLINE]
    19.

    Molecular analysis of aquaporin genes 1 to 4 in patients with Menière's disease.

    Candreia C, Schmuziger N, Gürtler N.

    Cell Physiol Biochem. 2010;26(4-5):787-92. Epub 2010 Oct 29.

    PMID:
    21063116
    [PubMed - indexed for MEDLINE]
    20.

    Induced endolymphatic flow from the endolymphatic sac to the cochlea in Ménière's disease.

    Mandalà M, Colletti L, Carner M, Cerini R, Barillari M, Mucelli RP, Colletti V.

    Otolaryngol Head Neck Surg. 2010 Nov;143(5):673-9.

    PMID:
    20974338
    [PubMed - indexed for MEDLINE]
    21.

    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. Epub 2010 Oct 7.

    PMID:
    20927121
    [PubMed - indexed for MEDLINE]
    22.

    Expression and translocation of aquaporin-2 in the endolymphatic sac in patients with Meniere's disease.

    Maekawa C, Kitahara T, Kizawa K, Okazaki S, Kamakura T, Horii A, Imai T, Doi K, Inohara H, Kiyama H.

    J Neuroendocrinol. 2010 Nov;22(11):1157-64. doi: 10.1111/j.1365-2826.2010.02060.x.

    PMID:
    20722976
    [PubMed - indexed for MEDLINE]
    23.

    Genetic investigations of Meniere's disease.

    Vrabec JT.

    Otolaryngol Clin North Am. 2010 Oct;43(5):1121-32. Review.

    PMID:
    20713249
    [PubMed - indexed for MEDLINE]
    24.

    Contemporary perspectives on the pathophysiology of Meniere's disease: implications for treatment.

    Semaan MT, Megerian CA.

    Curr Opin Otolaryngol Head Neck Surg. 2010 Oct;18(5):392-8. Review.

    PMID:
    20639763
    [PubMed - indexed for MEDLINE]
    25.

    Immunohistochemical localization and mRNA expression of aquaporins in the macula utriculi of patients with Meniere's disease and acoustic neuroma.

    Ishiyama G, Lopez IA, Beltran-Parrazal L, Ishiyama A.

    Cell Tissue Res. 2010 Jun;340(3):407-19. Epub 2010 May 12.

    PMID:
    20461409
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    26.

    HLA-B27-associated bilateral Ménière disease.

    Rawal SG, Thakkar KH, Ziai K, Santi PA, Djalilian HR.

    Ear Nose Throat J. 2010 Mar;89(3):122-7.

    PMID:
    20229477
    [PubMed - indexed for MEDLINE]
    27.

    Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population.

    Campbell CA, Della Santina CC, Meyer NC, Smith NB, Myrie OA, Stone EM, Fukushima K, Califano J, Carey JP, Hansen MR, Gantz BJ, Minor LB, Smith RJ.

    Am J Med Genet A. 2010 Jan;152A(1):67-74. Erratum in: Am J Med Genet A. 2011 Mar;155A(3):666.

    PMID:
    20034061
    [PubMed - indexed for MEDLINE]
    28.

    Chapter 50: history of tropical neurology.

    Ogunniyi A.

    Handb Clin Neurol. 2010;95:815-30.

    PMID:
    19892153
    [PubMed - indexed for MEDLINE]
    29.

    Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease.

    Lopez-Escamez JA, Moreno A, Bernal M, Perez-Garrigues H, Santos-Perez S, Soto-Varela A, Aran I, Fernandez-Sanfrancisco O, Lopez-Nevot A, Lopez-Nevot MA.

    Acta Otolaryngol. 2009 Nov;129(11):1222-5.

    PMID:
    19863315
    [PubMed - indexed for MEDLINE]
    30.

    [How to diagnose vertigo and dizziness].

    Strupp M, Jahn K, Zwergal A, Brandt T.

    MMW Fortschr Med. 2009 Sep 17;151(38):35-9. German. No abstract available.

    PMID:
    19831176
    [PubMed - indexed for MEDLINE]
    31.

    Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease.

    Lopez-Escamez JA, Saenz-Lopez P, Acosta L, Moreno A, Gazquez I, Perez-Garrigues H, Lopez-Nevot A, Lopez-Nevot MA.

    Laryngoscope. 2010 Jan;120(1):103-7.

    PMID:
    19780033
    [PubMed - indexed for MEDLINE]
    32.

    Coping with Meniere's disease: experience and benefits from the use of complementary and alternative medicine.

    Long AF, Bennett T.

    Chronic Illn. 2009 Sep;5(3):219-32. Epub 2009 Aug 12.

    PMID:
    19675117
    [PubMed - indexed for MEDLINE]
    33.

    Plasma vasopressin and V2 receptor in the endolymphatic sac in patients with delayed endolymphatic hydrops.

    Kitahara T, Maekawa C, Kizawa K, Horii A, Doi K.

    Otol Neurotol. 2009 Sep;30(6):812-9.

    PMID:
    19638944
    [PubMed - indexed for MEDLINE]
    34.

    Ménière's disease.

    Hamid MA.

    Pract Neurol. 2009 Jun;9(3):157-62.

    PMID:
    19448058
    [PubMed - indexed for MEDLINE]
    35.

    Polymorphic analysis of the heat-shock protein 70 gene (HSPA1A) in Ménière's disease.

    Kawaguchi S, Hagiwara A, Suzuki M.

    Acta Otolaryngol. 2008 Nov;128(11):1173-7.

    PMID:
    19241595
    [PubMed - indexed for MEDLINE]
    36.

    Expression of the osmotically responsive cationic channel TRPV4 in the endolymphatic sac.

    Kumagami H, Terakado M, Sainoo Y, Baba A, Fujiyama D, Fukuda T, Takasaki K, Takahashi H.

    Audiol Neurootol. 2009;14(3):190-7. Epub 2008 Dec 10.

    PMID:
    19066426
    [PubMed - indexed for MEDLINE]
    37.

    [Frequency of dizziness-related diagnoses and prescriptions in a general practice database].

    Kruschinski C, Kersting M, Breull A, Kochen MM, Koschack J, Hummers-Pradier E.

    Z Evid Fortbild Qual Gesundhwes. 2008;102(5):313-9. German.

    PMID:
    19006919
    [PubMed - indexed for MEDLINE]
    38.

    Large vestibular aqueduct syndrome and endolymphatic hydrops: two presentations of a common primary inner-ear dysfunction?

    Spiegel JH, Lalwani AK.

    J Laryngol Otol. 2009 Aug;123(8):919-21. Epub 2008 Nov 12. Review.

    PMID:
    19000343
    [PubMed - indexed for MEDLINE]
    39.

    Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Ménière's syndrome.

    Teggi R, Lanzani C, Zagato L, Delli Carpini S, Manunta P, Bianchi G, Bussi M.

    Otol Neurotol. 2008 Sep;29(6):824-8.

    PMID:
    18667944
    [PubMed - indexed for MEDLINE]
    40.

    Familial Ménière's disease: clinical and genetic aspects.

    Morrison AW, Bailey ME, Morrison GA.

    J Laryngol Otol. 2009 Jan;123(1):29-37. Epub 2008 Jul 11.

    PMID:
    18616841
    [PubMed - indexed for MEDLINE]
    41.

    Sequence variants in host cell factor C1 are associated with Ménière's disease.

    Vrabec JT, Liu L, Li B, Leal SM.

    Otol Neurotol. 2008 Jun;29(4):561-6.

    PMID:
    18520591
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    42.

    Soluble intercellular adhesion molecule 1 and soluble vascular cell adhesion molecule 1 in sudden hearing loss.

    Quaranta N, Ramunni A, Brescia P, D'Elia A, Vacca A, Ria R.

    Otol Neurotol. 2008 Jun;29(4):470-4.

    PMID:
    18401280
    [PubMed - indexed for MEDLINE]
    43.

    Migraine and Meniere's disease: two different phenomena with frequently observed concomitant occurrences.

    Ibekwe TS, Fasunla JA, Ibekwe PU, Obasikene GC, Onakoya PA, Nwaorgu OG.

    J Natl Med Assoc. 2008 Mar;100(3):334-8.

    PMID:
    18390027
    [PubMed - indexed for MEDLINE]
    44.

    Gene transfer in human vestibular epithelia and the prospects for inner ear gene therapy.

    Kesser BW, Hashisaki GT, Holt JR.

    Laryngoscope. 2008 May;118(5):821-31.

    PMID:
    18300702
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    45.

    A mouse model with postnatal endolymphatic hydrops and hearing loss.

    Megerian CA, Semaan MT, Aftab S, Kisley LB, Zheng QY, Pawlowski KS, Wright CG, Alagramam KN.

    Hear Res. 2008 Mar;237(1-2):90-105. Epub 2008 Jan 15.

    PMID:
    18289812
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    46.

    Do viruses cause inner ear disturbances?

    Pyykko I, Zou J.

    ORL J Otorhinolaryngol Relat Spec. 2008;70(1):32-40; discussion 40-1. Epub 2008 Feb 1.

    PMID:
    18235204
    [PubMed - indexed for MEDLINE]
    47.

    Herpes virus and Ménière's disease.

    Gartner M, Bossart W, Linder T.

    ORL J Otorhinolaryngol Relat Spec. 2008;70(1):28-31; discussion 31. Epub 2008 Feb 1.

    PMID:
    18235203
    [PubMed - indexed for MEDLINE]
    48.

    Recent advances in the genetics of recurrent vertigo and vestibulopathy.

    Jen JC.

    Curr Opin Neurol. 2008 Feb;21(1):3-7. Review.

    PMID:
    18180645
    [PubMed - indexed for MEDLINE]
    49.

    Familial clustering of migraine, episodic vertigo, and Ménière's disease.

    Cha YH, Kane MJ, Baloh RW.

    Otol Neurotol. 2008 Jan;29(1):93-6.

    PMID:
    18046258
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    50.

    Management of Ménière's disease in general practice: adherence to the UK National Health Service 'Prodigy' guidelines.

    Smale E, McDonald S, Maha N, Short S.

    J Laryngol Otol. 2008 Aug;122(8):780-5. Epub 2007 Nov 27.

    PMID:
    18039416
    [PubMed - indexed for MEDLINE]
    51.

    [Therapy with vasopressin receptor antagonists: the aquaretics.].

    Buemi M, Bolignano D, Coppolino G, Sturiale A, Campo S, Crasci' E, Aloisi C, Frisina N.

    G Ital Nefrol. 2007 Sep-Oct;24(5):371-80. Italian.

    PMID:
    17886207
    [PubMed - in process]
    52.

    The relevance of migraine in patients with Meńière's disease.

    Cha YH, Brodsky J, Ishiyama G, Sabatti C, Baloh RW.

    Acta Otolaryngol. 2007 Dec;127(12):1241-5.

    PMID:
    17851970
    [PubMed - indexed for MEDLINE]
    53.

    Migraine associated vertigo.

    Cha YH, Baloh RW.

    J Clin Neurol. 2007 Sep;3(3):121-6. Epub 2007 Sep 20.

    PMID:
    19513278
    [PubMed]
    Free PMC Article
    54.

    Survey of Ménière's disease in a subspecialty referral practice.

    Vrabec JT, Simon LM, Coker NJ.

    Otolaryngol Head Neck Surg. 2007 Aug;137(2):213-7.

    PMID:
    17666243
    [PubMed - indexed for MEDLINE]
    55.

    HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.

    Lopez-Escamez JA, Vilchez JR, Soto-Varela A, Santos-Perez S, Perez-Garrigues H, Aran I, Lopez-Nevot MA.

    Otol Neurotol. 2007 Oct;28(7):891-5.

    PMID:
    17592398
    [PubMed - indexed for MEDLINE]
    56.

    An in vitro model system to study gene therapy in the human inner ear.

    Kesser BW, Hashisaki GT, Fletcher K, Eppard H, Holt JR.

    Gene Ther. 2007 Aug;14(15):1121-31. Epub 2007 Jun 14.

    PMID:
    17568767
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    57.

    Familial unilateral deafness and delayed endolymphatic hydrops.

    Dodson KM, Kamei T, Sismanis A, Nance WE.

    Am J Med Genet A. 2007 Jul 15;143A(14):1661-5.

    PMID:
    17497713
    [PubMed - indexed for MEDLINE]
    58.

    Antibodies to myelin protein zero (P0) protein as markers of auto-immune inner ear diseases.

    Pham BN, Rudic M, Bouccara D, Sterkers O, Belmatoug N, Bébéar JP, Couloigner V, Fraysse B, Gentine A, Ionescu E, Robier A, Sauvage JP, Truy E, Van Den Abbeele T, Ferrary E.

    Autoimmunity. 2007 May;40(3):202-7.

    PMID:
    17453719
    [PubMed - indexed for MEDLINE]
    59.

    Aquaretic agents: what's beyond the treatment of hyponatremia?

    Bolignano D, Coppolino G, Criseo M, Campo S, Romeo A, Buemi M.

    Curr Pharm Des. 2007;13(8):865-71. Review.

    PMID:
    17430186
    [PubMed - indexed for MEDLINE]
    60.

    Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.

    Oki K, Nagata E, Ishiko A, Shimizu A, Tanaka K, Takahashi K, Tabira T, Katayama T, Suzuki N.

    Eur J Neurol. 2007 Apr;14(4):464-6.

    PMID:
    17389000
    [PubMed - indexed for MEDLINE]
    61.

    Aminoglycoside-induced ototoxicity.

    Selimoglu E.

    Curr Pharm Des. 2007;13(1):119-26. Review.

    PMID:
    17266591
    [PubMed - indexed for MEDLINE]
    62.

    Inheritance of Meniere's disease in the Finnish population.

    Klockars T, Kentala E.

    Arch Otolaryngol Head Neck Surg. 2007 Jan;133(1):73-7.

    PMID:
    17224529
    [PubMed - indexed for MEDLINE]
    Free Article
    63.

    Case report: Meniere's disease and otosclerosis--different outcomes of the same disease?

    Klockars T, Kentala E.

    Auris Nasus Larynx. 2007 Mar;34(1):101-4. Epub 2006 Nov 21.

    PMID:
    17118596
    [PubMed - indexed for MEDLINE]
    64.

    Effects of vasopressin on gene expression in rat inner ear.

    Gu FM, Han HL, Zhang LS.

    Hear Res. 2006 Dec;222(1-2):70-8. Epub 2006 Oct 25.

    PMID:
    17070001
    [PubMed - indexed for MEDLINE]
    65.

    Endolymphatic sac revision for recurrent intractable Meniere's disease.

    Paparella MM.

    Otolaryngol Clin North Am. 2006 Aug;39(4):713-21, vi. Review.

    PMID:
    16895780
    [PubMed - indexed for MEDLINE]
    66.

    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.

    PMID:
    16868516
    [PubMed - indexed for MEDLINE]
    67.

    Fabry's disease: otoneurologic findings in twelve members of one family.

    Vibert D, Blaser B, Ozdoba C, Häusler R.

    Ann Otol Rhinol Laryngol. 2006 Jun;115(6):412-8.

    PMID:
    16805371
    [PubMed - indexed for MEDLINE]
    68.

    Parallel auditory vestibular evoked neurogenic and myogenic potential results in a case of peripheral vestibular dysfunction, showing that the former originates from the vestibular system.

    Papathanasiou ES, Theocharidou EK, Papacostas SS.

    Electromyogr Clin Neurophysiol. 2006 Mar-Apr;46(2):105-11.

    PMID:
    16796000
    [PubMed - indexed for MEDLINE]
    69.

    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 5;141B(5):463-7.

    PMID:
    16741942
    [PubMed - indexed for MEDLINE]
    70.

    Initial evaluation of vertigo.

    Labuguen RH.

    Am Fam Physician. 2006 Jan 15;73(2):244-51. Review. Erratum in: Am Fam Physician. 2006 May 15;73(10):1704.

    PMID:
    16445269
    [PubMed - indexed for MEDLINE]
    Free Article
    71.

    Ménière's disease and various types of vertigo in children.

    Aust G, Novotný M.

    Int Tinnitus J. 2005;11(1):66-8. Review.

    PMID:
    16419694
    [PubMed - indexed for MEDLINE]
    72.

    Microarray analysis of stress-related gene expression in patients with Ménière's disease.

    Sekine K, Morita K, Masuda K, Sato G, Rokutan K, Takeda N.

    ORL J Otorhinolaryngol Relat Spec. 2005;67(5):294-9. Epub 2005 Dec 15.

    PMID:
    16374063
    [PubMed - indexed for MEDLINE]
    73.

    Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3.

    Doi K, Sato T, Kuramasu T, Hibino H, Kitahara T, Horii A, Matsushiro N, Fuse Y, Kubo T.

    ORL J Otorhinolaryngol Relat Spec. 2005;67(5):289-93. Epub 2005 Dec 15.

    PMID:
    16374062
    [PubMed - indexed for MEDLINE]
    74.

    Expression of cochlin in the vestibular organ of rats.

    Ikezono T, Shindo S, Ishizaki M, Li L, Tomiyama S, Takumida M, Pawankar R, Watanabe A, Saito A, Yagi T.

    ORL J Otorhinolaryngol Relat Spec. 2005;67(5):252-8.

    PMID:
    16374056
    [PubMed - indexed for MEDLINE]
    75.

    [From gene to disease; a progressive cochlear-vestibular dysfunction with onset in middle-age (DFNA9)].

    Cremers CW, Kemperman MH, Bom SJ, Huygen PL, Verhagen WI, Kremer JM.

    Ned Tijdschr Geneeskd. 2005 Nov 19;149(47):2619-21. Review. Dutch.

    PMID:
    16355574
    [PubMed - indexed for MEDLINE]
    76.

    Glucocorticoid regulation of genes in the amiloride-sensitive sodium transport pathway by semicircular canal duct epithelium of neonatal rat.

    Pondugula SR, Raveendran NN, Ergonul Z, Deng Y, Chen J, Sanneman JD, Palmer LG, Marcus DC.

    Physiol Genomics. 2006 Jan 12;24(2):114-23. Epub 2005 Nov 1.

    PMID:
    16263802
    [PubMed - indexed for MEDLINE]
    Free Article
    77.

    Hypothesis: could Meniere's disease be a channelopathy?

    Gates P.

    Intern Med J. 2005 Aug;35(8):488-9. Review.

    PMID:
    16176473
    [PubMed - indexed for MEDLINE]
    78.

    The basic science of Meniere's disease and endolymphatic hydrops.

    Semaan MT, Alagramam KN, Megerian CA.

    Curr Opin Otolaryngol Head Neck Surg. 2005 Oct;13(5):301-7. Review.

    PMID:
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    79.

    A reappraisal of the possible seizures of Vincent van Gogh.

    Hughes JR.

    Epilepsy Behav. 2005 Jun;6(4):504-10.

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    [Mutation on the 4th and 5th extrons of COCH gene in Meniere's disease].

    Sun Y, Liu B, Dai HJ, Liu Y, Du YS, Chen XW, Zhao LP.

    Zhonghua Yi Xue Za Zhi. 2005 Feb 2;85(5):345-7. Chinese. No abstract available.

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    81.

    Treatment of vertigo.

    Swartz R, Longwell P.

    Am Fam Physician. 2005 Mar 15;71(6):1115-22. Review.

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    [Cavernous haemangiomas: hearing and vestibular inaugural symptoms].

    Dumas G, Schmerber S.

    Ann Otolaryngol Chir Cervicofac. 2004 Nov;121(5):272-81. French.

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    Bell's palsy and Herpes simplex virus: fact or mystery?

    Linder T, Bossart W, Bodmer D.

    Otol Neurotol. 2005 Jan;26(1):109-13.

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    The genetics of hearing loss.

    Aggarwal R, Saeed SR.

    Hosp Med. 2005 Jan;66(1):32-6. Review.

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    Improvement of vestibular compensation by Levo-sulpiride in acute unilateral labyrinthine dysfunction.

    Zanetti D, Civiero N, Balzanelli C, Tonini M, Antonelli AR.

    Acta Otorhinolaryngol Ital. 2004 Apr;24(2):49-57.

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    [Chief symptom giddiness].

    Strupp M, Brandt T.

    MMW Fortschr Med. 2004 May 24;146 Spec No 2:47-9, 51. German.

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    87.

    Ménière's disease and anxiety disorders.

    Celestino D, Rosini E, Carucci ML, Marconi PL, Vercillo E.

    Acta Otorhinolaryngol Ital. 2003 Dec;23(6):421-7.

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    Endolymphatic sac tumors in von Hippel-Lindau disease.

    Choo D, Shotland L, Mastroianni M, Glenn G, van Waes C, Linehan WM, Oldfield EH.

    J Neurosurg. 2004 Mar;100(3):480-7.

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    Characteristics of tinnitus and etiology of associated hearing loss: a study of 123 patients.

    Nicolas-Puel C, Faulconbridge RL, Guitton M, Puel JL, Mondain M, Uziel A.

    Int Tinnitus J. 2002;8(1):37-44.

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    Vertigo and dizziness related to migraine: a diagnostic challenge.

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    Cephalalgia. 2004 Feb;24(2):83-91. Review.

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    Diagnostic approach to tinnitus.

    Crummer RW, Hassan GA.

    Am Fam Physician. 2004 Jan 1;69(1):120-6. Review.

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    Absence of COCH mutations in patients with Meniere disease.

    Sanchez E, López-Escámez JA, López-Nevot MA, López-Nevot A, Cortes R, Martin J.

    Eur J Hum Genet. 2004 Jan;12(1):75-8.

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    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.

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    Endolymphatic sac tumor in von Hippel-Lindau disease.

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    Otol Neurotol. 2003 Sep;24(5):832. No abstract available.

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    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;24(5):743-8.

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    Cell proliferation in the endolymphatic sac in situ after the rat Waldeyer ring equivalent immunostimulation.

    Yan Z, Wang JB, Gong SS, Huang X.

    Laryngoscope. 2003 Sep;113(9):1609-14.

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    Herpes simplex virus and Meniere's disease.

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    Laryngoscope. 2003 Sep;113(9):1431-8.

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    The effects of V2 antagonist (OPC-31260) on endolymphatic hydrops.

    Takeda T, Sawada S, Takeda S, Kitano H, Suzuki M, Kakigi A, Takeuchi S.

    Hear Res. 2003 Aug;182(1-2):9-18.

    PMID:
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    Detection of viral DNA in the endolymphatic sac in Ménière's disease by in situ hybridization.

    Yazawa Y, Suzuki M, Hanamitsu M, Kimura H, Tooyama I.

    ORL J Otorhinolaryngol Relat Spec. 2003 May-Jun;65(3):162-8.

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    Aquaporin-1 (AQP1) is expressed in the stria vascularis of rat cochlea.

    Sawada S, Takeda T, Kitano H, Takeuchi S, Okada T, Ando M, Suzuki M, Kakigi A.

    Hear Res. 2003 Jul;181(1-2):15-9.

    PMID:
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