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155 related items for PubMed ID: 9109727

  • 1. 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; 106(4):338-42. PubMed ID: 9109727
    [Abstract] [Full Text] [Related]

  • 2. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.
    Oshima T, Ueda N, Ikeda K, Abe K, Takasaka T.
    Laryngoscope; 1996 Jan; 106(1 Pt 1):43-8. PubMed ID: 8544626
    [Abstract] [Full Text] [Related]

  • 5. The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea.
    Iwasaki S, Egami N, Fujimoto C, Chihara Y, Ushio M, Kashio A, Yamasoba T.
    Laryngoscope; 2011 Aug; 121(8):1821-4. PubMed ID: 21792976
    [Abstract] [Full Text] [Related]

  • 6. Cochlear origin of hearing loss in MELAS syndrome.
    Sue CM, Lipsett LJ, Crimmins DS, Tsang CS, Boyages SC, Presgrave CM, Gibson WP, Byrne E, Morris JG.
    Ann Neurol; 1998 Mar; 43(3):350-9. PubMed ID: 9506552
    [Abstract] [Full Text] [Related]

  • 7. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.
    Yamasoba T, Oka Y, Tsukuda K, Nakamura M, Kaga K.
    Laryngoscope; 1996 Jan; 106(1 Pt 1):49-53. PubMed ID: 8544627
    [Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. Audiological findings in patients with myoclonic epilepsy associated with ragged-red fibres.
    Tsutsumi T, Nishida H, Noguchi Y, Komatsuzaki A, Kitamura K.
    J Laryngol Otol; 2001 Oct 30; 115(10):777-81. PubMed ID: 11667986
    [Abstract] [Full Text] [Related]

  • 10. A review of cochlear implantation in mitochondrial sensorineural hearing loss.
    Sinnathuray AR, Raut V, Awa A, Magee A, Toner JG.
    Otol Neurotol; 2003 May 30; 24(3):418-26. PubMed ID: 12806294
    [Abstract] [Full Text] [Related]

  • 11. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.
    Remes AM, Majamaa K, Herva R, Hassinen IE.
    Neurology; 1993 May 30; 43(5):1015-20. PubMed ID: 8492919
    [Abstract] [Full Text] [Related]

  • 12. Sensorineural hearing loss in MELAS syndrome--case report.
    Chen JN, Ho KY, Juan KH.
    Kaohsiung J Med Sci; 1998 Aug 30; 14(8):519-23. PubMed ID: 9780603
    [Abstract] [Full Text] [Related]

  • 13. [Audiologic evaluation in a family showing diabetes mellitus and deafness associated with a mutation in mitochondrial DNA].
    Tamagawa Y, Tanaka H, Hagiwara H, Ishida T, Kitamura K.
    Nihon Jibiinkoka Gakkai Kaiho; 1995 Aug 30; 98(8):1257-62. PubMed ID: 7472762
    [Abstract] [Full Text] [Related]

  • 14. The Finnish speech-in-noise test in MELAS mutation and other sensorineural hearing impairments.
    Uimonen S, Laitakari K, Majamaa K.
    Scand Audiol Suppl; 2001 Aug 30; (52):83-4. PubMed ID: 11318493
    [Abstract] [Full Text] [Related]

  • 15. 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 30; 18(3):332-5. PubMed ID: 9149827
    [Abstract] [Full Text] [Related]

  • 16. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M, Díaz-Guzmán J, Pérez-Martínez DA, Sáiz-Díaz RA, Rodríguez-Vallejo A, Campos Y.
    Rev Neurol; 1997 May 30; 33(2):148-50. PubMed ID: 11562875
    [Abstract] [Full Text] [Related]

  • 17. 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 30; 68(8):1115-9. PubMed ID: 15236904
    [Abstract] [Full Text] [Related]

  • 18. Auditory neuropathy in childhood.
    Doyle KJ, Sininger Y, Starr A.
    Laryngoscope; 1998 Sep 30; 108(9):1374-7. PubMed ID: 9738760
    [Abstract] [Full Text] [Related]

  • 19. [Unexceptional symptoms as expression of MELAS].
    van Rossum IA, ten Houten R.
    Ned Tijdschr Geneeskd; 2010 Sep 30; 154():A2168. PubMed ID: 21083956
    [Abstract] [Full Text] [Related]

  • 20. 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 30; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

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