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Journal Abstract Search

113 related items for PubMed ID: 3147507

  • 1. Incidence of genetic factors in the causation of deafness in childhood.
    Lenzi A, Zaghis A.
    Scand Audiol Suppl; 1988; 30():37-41. PubMed ID: 3147507
    [Abstract] [Full Text] [Related]

  • 2. Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life.
    Nance WE, Sweeney A.
    Otolaryngol Clin North Am; 1975 Feb; 8(1):19-48. PubMed ID: 1090886
    [Abstract] [Full Text] [Related]

  • 3. Symposium on sensorineural hearing loss in children: early detection and intervention. Histopathology of sensorineural hearing loss in children.
    Altenau MM.
    Otolaryngol Clin North Am; 1975 Feb; 8(1):49-58. PubMed ID: 1118165
    [Abstract] [Full Text] [Related]

  • 4. Genetic disposition to deafness in maternal rubella: fact or myth?
    Moroso MJ.
    J Otolaryngol; 1985 Feb; 14(1):44-8. PubMed ID: 4068090
    [Abstract] [Full Text] [Related]

  • 5. [Hereditary diseases of the otorhinolaryngologic organs (review of the literature)].
    Bariliak IR, Bariliak IuR.
    Zh Ushn Nos Gorl Bolezn; 1972 Feb; 32(1):113-20. PubMed ID: 4553121
    [No Abstract] [Full Text] [Related]

  • 6. A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I.
    Otterstedde CR, Spandau U, Blankenagel A, Kimberling WJ, Reisser C.
    Laryngoscope; 2001 Jan; 111(1):84-6. PubMed ID: 11192904
    [Abstract] [Full Text] [Related]

  • 7. The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).
    Kloepfer HW, Laguaite JK.
    Laryngoscope; 1966 May; 76(5):850-62. PubMed ID: 5937908
    [No Abstract] [Full Text] [Related]

  • 8. Hearing assessment in pre-school children with speech delay.
    Psillas G, Psifidis A, Antoniadou-Hitoglou M, Kouloulas A.
    Auris Nasus Larynx; 2006 Sep; 33(3):259-63. PubMed ID: 16420975
    [Abstract] [Full Text] [Related]

  • 9. [Diagnosis of hearing disorders in children with early evoked auditory brainstem potentials].
    Savić L, Milosević D, Komazec Z.
    Med Pregl; 1999 Sep; 52(3-5):146-50. PubMed ID: 10518400
    [Abstract] [Full Text] [Related]

  • 10. Pattern of childhood deafness in an audiologic centre in Port Harcourt, Nigeria.
    Alikor EA, Otana AO.
    Niger J Med; 2005 Sep; 14(3):307-10. PubMed ID: 16350704
    [Abstract] [Full Text] [Related]

  • 11. [Clinical examinations in Usher's syndrome].
    Lubiński W, Palacz O, Zajaczek S.
    Klin Oczna; 1996 Jan; 98(1):55-8. PubMed ID: 9019578
    [Abstract] [Full Text] [Related]

  • 12. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 13. [Etiologic problems of hearing disorders in "risk children"].
    Beckmann G.
    HNO; 1969 Aug; 17(8):225-9. PubMed ID: 4996331
    [No Abstract] [Full Text] [Related]

  • 14. From hearing screening to cochlear implantation: cochlear implants in children under 3 years of age.
    Profant M, Kabátová Z, Simková L.
    Acta Otolaryngol; 2008 Apr; 128(4):369-72. PubMed ID: 18368567
    [Abstract] [Full Text] [Related]

  • 15. [Cardio-auditory syndromes of genetic origin].
    Pernot C, Henry M, Debruille C.
    Coeur Med Interne; 1974 Apr; 13(3):429-43. PubMed ID: 4140046
    [No Abstract] [Full Text] [Related]

  • 16. [Diagnosing hearing impairment in children].
    Hempel JM.
    MMW Fortschr Med; 2006 May 11; 148(19):26-8, 30. PubMed ID: 16736701
    [Abstract] [Full Text] [Related]

  • 17. Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.
    Shaukat S, Fatima Z, Zehra U, Waqar AB.
    J Ayub Med Coll Abbottabad; 2003 May 11; 15(3):59-64. PubMed ID: 14727345
    [Abstract] [Full Text] [Related]

  • 18. [The Jervell- and Lange-Nielsen syndrome. A peculiar form of hereditary cardio-myopathy].
    Athanasiou DJ, Weiner C.
    Munch Med Wochenschr; 1972 Apr 14; 114(15):698-706. PubMed ID: 5068323
    [No Abstract] [Full Text] [Related]

  • 19. Vestibular system in infants with hereditary nonsyndromic deafness.
    Zagólski O.
    Otol Neurotol; 2007 Dec 14; 28(8):1053-5. PubMed ID: 17898670
    [Abstract] [Full Text] [Related]

  • 20. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area].
    Oeken J, König E.
    HNO; 1993 Jun 14; 41(6):301-10. PubMed ID: 8365917
    [Abstract] [Full Text] [Related]

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