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Journal Abstract Search

133 related items for PubMed ID: 9639482

  • 21. Relationship Between Audio-Vestibular Functional Tests and Inner Ear MRI in Meniere's Disease.
    Quatre R, Attyé A, Karkas A, Job A, Dumas G, Schmerber S.
    Ear Hear; 2019; 40(1):168-176. PubMed ID: 29698363
    [Abstract] [Full Text] [Related]

  • 22. Unilateral sensorineural hearing loss in children: the importance of temporal bone computed tomography and audiometric follow-up.
    Song JJ, Choi HG, Oh SH, Chang SO, Kim CS, Lee JH.
    Otol Neurotol; 2009 Aug; 30(5):604-8. PubMed ID: 19546828
    [Abstract] [Full Text] [Related]

  • 23. Distortion-product otoacoustic emissions and glycerol testing in endolymphatic hydrops.
    Magliulo G, Cianfrone G, Triches L, Altissimi G, D'Amico R.
    Laryngoscope; 2001 Jan; 111(1):102-9. PubMed ID: 11192876
    [Abstract] [Full Text] [Related]

  • 24. Sacculo-collic pathway dysfunction accompanying auditory neuropathy.
    Sheykholeslami K, Schmerber S, Habiby Kermany M, Kaga K.
    Acta Otolaryngol; 2005 Jul; 125(7):786-91. PubMed ID: 16012043
    [Abstract] [Full Text] [Related]

  • 25. Evaluation of Patients with Delayed Endolymphatic Hydrops by Videonystagmography, Vestibular-Evoked Myogenic Potentials, and Electrocochleography.
    Yazdani N, Rahmaty B, Mousavi M, Aghazadeh K, Dabiri S, Erfanian R, Jafari N, Rezazadeh N, Tajdini A, Givzadeh H.
    ORL J Otorhinolaryngol Relat Spec; 2021 Jul; 83(4):242-251. PubMed ID: 33730714
    [Abstract] [Full Text] [Related]

  • 26. Audiovestibular sequelae of congenital cytomegalovirus infection in 3 children presumably representing 3 symptomatically different types of delayed endolymphatic hydrops.
    Huygen PL, Admiraal RJ.
    Int J Pediatr Otorhinolaryngol; 1996 Apr; 35(2):143-54. PubMed ID: 8735410
    [Abstract] [Full Text] [Related]

  • 27. Differentiating the cause of acute sensorineural hearing loss between Ménière's disease and sudden deafness.
    Chen CN, Young YH.
    Acta Otolaryngol; 2006 Jan; 126(1):25-31. PubMed ID: 16308251
    [Abstract] [Full Text] [Related]

  • 28. Patient with an SLC26A4 gene mutation who had low-frequency sensorineural hearing loss and endolymphatic hydrops.
    Yoshida T, Sone M, Naganawa S, Nakashima T.
    J Laryngol Otol; 2015 Jan; 129(1):95-7. PubMed ID: 25572613
    [Abstract] [Full Text] [Related]

  • 29. Distortion-product otoacoustic emissions and cochlear microphonics: relationships in patients with and without endolymphatic hydrops.
    Fetterman BL.
    Laryngoscope; 2001 Jun; 111(6):946-54. PubMed ID: 11404602
    [Abstract] [Full Text] [Related]

  • 30. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ, Mudde AH, 't Hart LM, Huygen PL, Cremers CW.
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

  • 31. Neurophysiologic, audiometric and vestibular function tests in patients with hyperostosis cranialis interna.
    Waterval JJ, Bischoff MP, Stokroos RJ, Anteunis LJ, Hilkman DM, Kingma H, Manni JJ.
    Clin Neurol Neurosurg; 2013 Sep; 115(9):1701-8. PubMed ID: 23622937
    [Abstract] [Full Text] [Related]

  • 32. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
    [Abstract] [Full Text] [Related]

  • 33. 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. PubMed ID: 17497713
    [Abstract] [Full Text] [Related]

  • 34. Auditory dysfunction in Stickler syndrome.
    Szymko-Bennett YM, Mastroianni MA, Shotland LI, Davis J, Ondrey FG, Balog JZ, Rudy SF, McCullagh L, Levy HP, Liberfarb RM, Francomano CA, Griffith AJ.
    Arch Otolaryngol Head Neck Surg; 2001 Sep 15; 127(9):1061-8. PubMed ID: 11556853
    [Abstract] [Full Text] [Related]

  • 35. Phenotypes of two Dutch DFNA3 families with mutations in GJB2.
    Weegerink NJ, Pennings RJ, Huygen PL, Hoefsloot LH, Cremers CW, Kunst HP.
    Ann Otol Rhinol Laryngol; 2011 Mar 15; 120(3):191-7. PubMed ID: 21510145
    [Abstract] [Full Text] [Related]

  • 36. Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor.
    Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB.
    Arch Otolaryngol Head Neck Surg; 2000 May 15; 126(5):633-7. PubMed ID: 10807331
    [Abstract] [Full Text] [Related]

  • 37. [Visualization of endolymphatic hydrops in 3D-FLAIR MRI after intratympanic Gd-DTPA administration in Meniere's disease patients].
    Zhang DG, Shi HL, Fan ZM, Wang GB, Han YC, Li YW, Wang HB.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Aug 15; 48(8):628-33. PubMed ID: 24195817
    [Abstract] [Full Text] [Related]

  • 38. In vivo visualized endolymphatic hydrops and inner ear functions in patients with electrocochleographically confirmed Ménière's disease.
    Gürkov R, Flatz W, Louza J, Strupp M, Ertl-Wagner B, Krause E.
    Otol Neurotol; 2012 Aug 15; 33(6):1040-5. PubMed ID: 22772006
    [Abstract] [Full Text] [Related]

  • 39. Spontaneous otoacoustic emissions in humans with endolymphatic hydrops.
    Haginomori SI, Makimoto K, Tanaka H, Araki M, Takenaka H.
    Laryngoscope; 2001 Jan 15; 111(1):96-101. PubMed ID: 11192908
    [Abstract] [Full Text] [Related]

  • 40. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
    Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ.
    J Assoc Res Otolaryngol; 2007 Mar 15; 8(1):1-7. PubMed ID: 17136632
    [Abstract] [Full Text] [Related]

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