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Journal Abstract Search

88 related items for PubMed ID: 9149827

  • 1. Audiological findings of sensorineural deafness associated with a mutation in the mitochondrial DNA.
    Sawada S, Takeda T, Kakigi A, Saito H, Suehiro T, Nakauchi Y, Chikamori K.
    Am J Otol; 1997 May; 18(3):332-5. PubMed ID: 9149827
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [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; 35(2):98-101. PubMed ID: 12768662
    [Abstract] [Full Text] [Related]

  • 4. [Audiological characteristics of auditory neuropathy].
    Wang J, Duan J, Li Q, Huang X, Chen H, Jin J, Gong S, Kong W.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Aug; 37(4):252-5. PubMed ID: 12772407
    [Abstract] [Full Text] [Related]

  • 5. Hearing evaluation in two sisters with a T8993G point mutation of mitochondrial DNA.
    Sakai Y, Kaga K, Kodama K, Higuchi A, Miyamoto J.
    Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):1115-9. PubMed ID: 15236904
    [Abstract] [Full Text] [Related]

  • 6. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies.
    Zwirner P, Wilichowski E.
    Laryngoscope; 2001 Mar; 111(3):515-21. PubMed ID: 11224785
    [Abstract] [Full Text] [Related]

  • 7. A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.
    Reid FM, Vernham GA, Jacobs HT.
    Hum Mutat; 1994 Mar; 3(3):243-7. PubMed ID: 8019558
    [Abstract] [Full Text] [Related]

  • 8. 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; 19(6):754-7. PubMed ID: 9831149
    [Abstract] [Full Text] [Related]

  • 9. Comparison of auditory steady-state responses and auditory brainstem responses in audiometric assessment of adults with sensorineural hearing loss.
    Lin YH, Ho HC, Wu HP.
    Auris Nasus Larynx; 2009 Apr; 36(2):140-5. PubMed ID: 18620826
    [Abstract] [Full Text] [Related]

  • 10. [Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate].
    Xue JF, Chen L, Ma YN, Zhao DH, Duan JB, Wang ZX, Qi Y, Liu YH.
    Zhonghua Yi Xue Za Zhi; 2012 Oct 30; 92(40):2830-4. PubMed ID: 23290211
    [Abstract] [Full Text] [Related]

  • 11. Correlations between audiogram and objective hearing tests in sensorineural hearing loss.
    Bishara L, Ben-David J, Podoshin L, Fradis M, Teszler CB, Pratt H, Shpack T, Feiglin H, Hafner H, Herlinger N.
    Int Tinnitus J; 1999 Oct 30; 5(2):107-12. PubMed ID: 10753428
    [Abstract] [Full Text] [Related]

  • 12. Mitochondrial diabetes and deafness: possible dysfunction of strial marginal cells of the inner ear.
    Olmos PR, Borzone GR, Olmos JP, Diez A, Santos JL, Serrano V, Cataldo LR, Anabalón JL, Correa CH.
    J Otolaryngol Head Neck Surg; 2011 Apr 30; 40(2):93-103. PubMed ID: 21453644
    [Abstract] [Full Text] [Related]

  • 13. Auditory cortical responses evoked by pure tones in healthy and sensorineural hearing loss subjects: functional MRI and magnetoencephalography.
    Zhang YT, Geng ZJ, Zhang Q, Li W, Zhang J.
    Chin Med J (Engl); 2006 Sep 20; 119(18):1548-54. PubMed ID: 16996009
    [Abstract] [Full Text] [Related]

  • 14. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun 20; 28(3):332-42. PubMed ID: 17485982
    [Abstract] [Full Text] [Related]

  • 15. Results of cochlear implantation in two children with mutations in the OTOF gene.
    Rouillon I, Marcolla A, Roux I, Marlin S, Feldmann D, Couderc R, Jonard L, Petit C, Denoyelle F, Garabédian EN, Loundon N.
    Int J Pediatr Otorhinolaryngol; 2006 Apr 20; 70(4):689-96. PubMed ID: 16226319
    [Abstract] [Full Text] [Related]

  • 16. Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.
    Tamagawa Y, Kitamura K, Hagiwara H, Ishida T, Nishizawa M, Saito T, Iwamoto Y.
    Ann Otol Rhinol Laryngol; 1997 Apr 20; 106(4):338-42. PubMed ID: 9109727
    [Abstract] [Full Text] [Related]

  • 17. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
    Nagata H, Kumahara K, Tomemori T, Arimoto Y, Isoyama K, Yoshida K, Konno A.
    J Hum Genet; 2001 Apr 20; 46(10):595-9. PubMed ID: 11587074
    [Abstract] [Full Text] [Related]

  • 18. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep 20; 113(9):1623-9. PubMed ID: 12972945
    [Abstract] [Full Text] [Related]

  • 19. 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 20; 8(1):1-7. PubMed ID: 17136632
    [Abstract] [Full Text] [Related]

  • 20. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.
    Biochem Biophys Res Commun; 1998 Apr 17; 245(2):523-7. PubMed ID: 9571188
    [Abstract] [Full Text] [Related]

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