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

96 related items for PubMed ID: 14755216

  • 1. Audiovestibular findings in patients with mitochondrial A1555G mutation.
    Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K.
    Laryngoscope; 2004 Feb; 114(2):344-8. PubMed ID: 14755216
    [Abstract] [Full Text] [Related]

  • 2. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
    [Abstract] [Full Text] [Related]

  • 3. Vestibular evoked myogenic potentials in patients with the mitochondrial A1555G mutation.
    Kawashima Y, Noguchi Y, Ito T, Kitamura K.
    Laryngoscope; 2009 Sep 02; 119(9):1874-9. PubMed ID: 19536740
    [Abstract] [Full Text] [Related]

  • 4. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S.
    Laryngoscope; 2004 Jun 02; 114(6):1085-91. PubMed ID: 15179218
    [Abstract] [Full Text] [Related]

  • 5. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation.
    Tono T, Ushisako Y, Kiyomizu K, Usami S, Abe S, Shinkawa H, Komune S.
    Am J Otol; 1998 Nov 02; 19(6):754-7. PubMed ID: 9831149
    [Abstract] [Full Text] [Related]

  • 6. Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.
    Ishikawa K, Tamagawa Y, Takahashi K, Kimura H, Kusakari J, Hara A, Ichimura K.
    Laryngoscope; 2002 Aug 02; 112(8 Pt 1):1494-9. PubMed ID: 12172268
    [Abstract] [Full Text] [Related]

  • 7. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA, Furze AD, Angeli SI.
    J Laryngol Otol; 2006 Mar 02; 120(3):230-2. PubMed ID: 16359140
    [Abstract] [Full Text] [Related]

  • 8. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].
    Xing G, Bu X, Yan M, Lu L, Yang S.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr 02; 35(2):98-101. PubMed ID: 12768662
    [Abstract] [Full Text] [Related]

  • 9. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
    Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct 02; 26(5):550-4. PubMed ID: 19806580
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S, Forli F, Passetti S, Rocchi A, Pollina L, Cecchetti D, Mancuso M, Siciliano G.
    Biosci Rep; 2008 Feb 02; 28(1):49-59. PubMed ID: 18215147
    [Abstract] [Full Text] [Related]

  • 11. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH, Reddy PP.
    Int J Audiol; 2008 Nov 02; 47(11):702-7. PubMed ID: 19031229
    [Abstract] [Full Text] [Related]

  • 12. 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 02; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
    Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M.
    Hum Mutat; 2002 Mar 02; 19(3):308-9. PubMed ID: 11857751
    [Abstract] [Full Text] [Related]

  • 17. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
    Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S.
    Auris Nasus Larynx; 2005 Jun 02; 32(2):119-24. PubMed ID: 15917167
    [Abstract] [Full Text] [Related]

  • 18. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 19. [Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)].
    Morales Angulo C, Gallo Terán J, del Castillo I, Moreno Pelayo MA, García-Mantilla J, Moreno Herrero F.
    Acta Otorrinolaringol Esp; 2002 Nov 03; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 20. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S.
    Ann Otol Rhinol Laryngol; 2005 Feb 03; 114(2):153-60. PubMed ID: 15757197
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.