These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

115 related items for PubMed ID: 21433022

  • 1. Phenotype of the first otosclerosis family linked to OTSC10.
    Weegerink NJ, Schrauwen I, Huygen PL, Pennings RJ, Cremers CW, Van Camp G, Kunst HP.
    Laryngoscope; 2011 Apr; 121(4):838-45. PubMed ID: 21433022
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree.
    Iliadou V, Van Den Bogaert K, Eleftheriades N, Aperis G, Vanderstraeten K, Fransen E, Thys M, Grigoriadou M, Pampanos A, Economides J, Iliades T, Van Camp G, Petersen MB.
    Int J Pediatr Otorhinolaryngol; 2006 Apr; 70(4):631-7. PubMed ID: 16168495
    [Abstract] [Full Text] [Related]

  • 4. The phenotype of the first otosclerosis family linked to OTSC5.
    Pauw RJ, De Leenheer EM, Van Den Bogaert K, Huygen PL, Van Camp G, Joosten FB, Cremers CW.
    Otol Neurotol; 2006 Apr; 27(3):308-15. PubMed ID: 16639267
    [Abstract] [Full Text] [Related]

  • 5. Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families.
    Di Leva F, D'Adamo AP, Strollo L, Auletta G, Caravelli A, Carella M, Mari F, Livi W, Renieri A, Gasparini P, D'Urso M, Marciano E, Franzé A.
    Int J Audiol; 2003 Dec; 42(8):475-80. PubMed ID: 14658855
    [Abstract] [Full Text] [Related]

  • 6. Early detection of otosclerosis by impedance-audiometry screening.
    Causse JR, Causse JB.
    Scand Audiol Suppl; 1983 Dec; 17():47-54. PubMed ID: 6577559
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Otospongiosis as a genetic disease. Early detection, medical management, and prevention.
    Causse JR, Causse JB.
    Am J Otol; 1984 Jan; 5(3):211-23. PubMed ID: 6372501
    [Abstract] [Full Text] [Related]

  • 11. Negative needle deflection of the acoustic reflex in otosclerotics.
    Rane RL, Yut JP, Berger KW.
    J Am Audiol Soc; 1978 Jan; 3(6):241-4. PubMed ID: 681195
    [Abstract] [Full Text] [Related]

  • 12. Audiometric analyses confirm a cochlear component, disproportional to age, in stapedial otosclerosis.
    Topsakal V, Fransen E, Schmerber S, Declau F, Yung M, Gordts F, Van Camp G, Van de Heyning P.
    Otol Neurotol; 2006 Sep; 27(6):781-7. PubMed ID: 16885785
    [Abstract] [Full Text] [Related]

  • 13. Otosclerosis--the last four years.
    Wiet RJ, Causse JB.
    Am J Otol; 1982 Jan; 3(3):249-55. PubMed ID: 7034545
    [No Abstract] [Full Text] [Related]

  • 14. [Audiological diagnosis of rarely occurring pathological conditions of the ear ossicles].
    Savel'eva EV, Shurovskiĭ VV.
    Vestn Otorinolaringol; 1988 Jan; (2):68-71. PubMed ID: 3388677
    [No Abstract] [Full Text] [Related]

  • 15. A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1.
    Thys M, Van Den Bogaert K, Iliadou V, Vanderstraeten K, Dieltjens N, Schrauwen I, Chen W, Eleftheriades N, Grigoriadou M, Pauw RJ, Cremers CR, Smith RJ, Petersen MB, Van Camp G.
    Eur J Hum Genet; 2007 Mar; 15(3):362-8. PubMed ID: 17213839
    [Abstract] [Full Text] [Related]

  • 16. Impedance transfer: acoustic impedance of the annular ligament and stapedial tendon reconstruction in otosclerosis surgery.
    Causse JB, Gherini S, Lopez A, Juberthie L, Olivier JC, Bastianelli G.
    Am J Otol; 1993 Nov; 14(6):613-7. PubMed ID: 8296869
    [Abstract] [Full Text] [Related]

  • 17. Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta.
    Swinnen FK, De Leenheer EM, Coucke PJ, Cremers CW, Dhooge IJ.
    Laryngoscope; 2009 Jun; 119(6):1171-9. PubMed ID: 19358256
    [Abstract] [Full Text] [Related]

  • 18. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
    [Abstract] [Full Text] [Related]

  • 19. Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.
    Topsakal V, Hilgert N, van Dinther J, Tranebjaerg L, Rendtorff ND, Zarowski A, Offeciers E, Van Camp G, van de Heyning P.
    Audiol Neurootol; 2010 Sep; 15(4):211-20. PubMed ID: 19893302
    [Abstract] [Full Text] [Related]

  • 20. Laser stapedotomy minus prosthesis (laser STAMP): a minimally invasive procedure.
    Silverstein H.
    Am J Otol; 1998 May; 19(3):277-82. PubMed ID: 9596174
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.