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Journal Abstract Search

182 related items for PubMed ID: 15895791

  • 1. Hereditary congenital unilateral deafness: a new disorder?
    Dikkers FG, Verheij JB, van Mechelen M.
    Ann Otol Rhinol Laryngol; 2005 Apr; 114(4):332-7. PubMed ID: 15895791
    [Abstract] [Full Text] [Related]

  • 2. Inner ear histopathology in genetically determined congenital deafness.
    Lindsay JR.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):21-32. PubMed ID: 5173349
    [Abstract] [Full Text] [Related]

  • 3. Computed tomographic findings of X-linked deafness: a spectrum from child to mother, from young to old, from boy to girl, from mixed to sudden hearing loss.
    Saylisoy S, Incesulu A, Gurbuz MK, Adapinar B.
    J Comput Assist Tomogr; 2014 Mar; 38(1):20-4. PubMed ID: 24424552
    [Abstract] [Full Text] [Related]

  • 4. [Diagnosis and operative sequela of rare abnormalities of the inner ear].
    Ptok A, Kahle G.
    HNO; 1986 Mar; 34(3):118-24. PubMed ID: 3700143
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  • 5. [Constitute, imaging and auditory characteristics of pediatric patients with congenital malformations of inner ear in sensorineural hearing loss].
    Li Y, Yang J, Li Y.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Jan; 25(1):1-5. PubMed ID: 21469382
    [Abstract] [Full Text] [Related]

  • 6. Radiological Imaging Findings of Patients with Congenital Totally Hearing Loss.
    Dağkıran M, Dağkıran N, Sürmelioğlu Ö, Ballı T, Tuncer Ü, Akgül E, Çetik F.
    J Int Adv Otol; 2016 Apr; 12(1):43-8. PubMed ID: 27340982
    [Abstract] [Full Text] [Related]

  • 7. Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides.
    Braverman I, Jaber L, Levi H, Adelman C, Arons KS, Fischel-Ghodsian N, Shohat M, Elidan J.
    Arch Otolaryngol Head Neck Surg; 1996 Sep; 122(9):1001-4. PubMed ID: 8797567
    [Abstract] [Full Text] [Related]

  • 8. Radiological malformations of the ear in Pendred syndrome.
    Phelps PD, Coffey RA, Trembath RC, Luxon LM, Grossman AB, Britton KE, Kendall-Taylor P, Graham JM, Cadge BC, Stephens SG, Pembrey ME, Reardon W.
    Clin Radiol; 1998 Apr; 53(4):268-73. PubMed ID: 9585042
    [Abstract] [Full Text] [Related]

  • 9. [A report of two familial cases of Michel syndrome (bilateral agenesis of the inner ear)].
    Ghazli K, Merite-Drancy A, Marsot-Dupuch K, Meyer B, Jeunesse Y, Chouard CH.
    Ann Otolaryngol Chir Cervicofac; 1998 Feb; 115(1):29-34. PubMed ID: 9765708
    [Abstract] [Full Text] [Related]

  • 10. Vestibular system in infants with hereditary nonsyndromic deafness.
    Zagólski O.
    Otol Neurotol; 2007 Dec; 28(8):1053-5. PubMed ID: 17898670
    [Abstract] [Full Text] [Related]

  • 11. [Deafness caused by malformation of the inner ear. Current contribution of x-ray computed tomography].
    Triglia JM, Nicollas R, Ternier F, Cannoni M.
    Ann Otolaryngol Chir Cervicofac; 1993 Dec; 110(5):241-6. PubMed ID: 8304695
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  • 15. [Hereditary deafness with electronystagmographic changes].
    Amendolea L.
    Valsalva; 1968 Dec; 44(6):356-69. PubMed ID: 5718915
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  • 17. Congenital neural hearing-loss due to inner ear malformation.
    Brama I.
    J Laryngol Otol; 1985 Mar; 99(3):293-5. PubMed ID: 3973500
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