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Journal Abstract Search

81 related items for PubMed ID: 24770403

  • 1. High-frequency involved hearing loss caused by novel mitochondrial DNA mutation in 16S ribosomal RNA gene.
    Abe S, Nagano M, Nishio SY, Kumakawa K, Usami S.
    Otol Neurotol; 2014 Jul; 35(6):1087-90. PubMed ID: 24770403
    [Abstract] [Full Text] [Related]

  • 2. 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; 28(3):332-42. PubMed ID: 17485982
    [Abstract] [Full Text] [Related]

  • 3. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.
    Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX.
    J Med Genet; 2011 Oct; 48(10):682-90. PubMed ID: 21931169
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5. Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment.
    Lehtonen MS, Uimonen S, Hassinen IE, Majamaa K.
    Eur J Hum Genet; 2000 Apr; 8(4):315-8. PubMed ID: 10854117
    [Abstract] [Full Text] [Related]

  • 6. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
    Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF, Dollfus H, Eliot MM, Faivre L, Duvillard C, Couderc R, Garabedian EN, Petit C, Feldmann D, Denoyelle F.
    Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
    [Abstract] [Full Text] [Related]

  • 7. Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
    Verhoeven K, Ensink RJ, Tiranti V, Huygen PL, Johnson DF, Schatteman I, Van Laer L, Verstreken M, Van de Heyning P, Fischel-Ghodsian N, Zeviani M, Cremers CW, Willems PJ, Van Camp G.
    Eur J Hum Genet; 1999 Jan; 7(1):45-51. PubMed ID: 10094190
    [Abstract] [Full Text] [Related]

  • 8. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
    Eur J Hum Genet; 1998 Jan; 6(6):563-9. PubMed ID: 9887373
    [Abstract] [Full Text] [Related]

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  • 10. Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.
    Mkaouar-Rebai E, Fendri-Kriaa N, Louhichi N, Tlili A, Triki C, Ghorbel A, Masmoudi S, Fakhfakh F.
    Biosci Rep; 2010 Dec; 30(6):405-11. PubMed ID: 20055758
    [Abstract] [Full Text] [Related]

  • 11. [Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].
    Cao X, Xing GQ, Wei QJ, Bu XK, Wang DY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):629-32. PubMed ID: 15583999
    [Abstract] [Full Text] [Related]

  • 12. Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.
    Labay V, Garrido G, Madeo AC, Nance WE, Friedman TB, Friedman PL, Del Castillo I, Griffith AJ.
    Clin Genet; 2008 Jan; 73(1):50-4. PubMed ID: 18028453
    [Abstract] [Full Text] [Related]

  • 13. Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.
    Li R, Ishikawa K, Deng JH, Heman-Ackah S, Tamagawa Y, Yang L, Bai Y, Ichimura K, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 04; 328(1):32-7. PubMed ID: 15670746
    [Abstract] [Full Text] [Related]

  • 14. Hereditary sensorineural hearing loss of unknown cause involving mitochondrial DNA 1555 mutation.
    Iwasaki S, Tamagawa Y, Ocho S, Hoshino T, Kitamura K.
    ORL J Otorhinolaryngol Relat Spec; 2000 Mar 04; 62(2):100-3. PubMed ID: 10729800
    [Abstract] [Full Text] [Related]

  • 15. [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].
    Dzhemileva LU, Posukh OL, Tazetdinov AM, Barashkov NA, Zhuravskiĭ SG, Ponidelko SN, Markova TG, Tadinova VN, Fedorova SA, Maksimova NR, Khusnutdinova EK.
    Genetika; 2009 Jul 04; 45(7):982-91. PubMed ID: 19705751
    [Abstract] [Full Text] [Related]

  • 16. [Non-syndromic familial hearing impairment transmitted by mitochondrial inheritance].
    Morales Angulo C, Del Castillo I, Sarduy M, Villamar M, Mazón A, Moreno F.
    Acta Otorrinolaringol Esp; 1999 Mar 04; 50(2):93-9. PubMed ID: 10217681
    [Abstract] [Full Text] [Related]

  • 17. Hearing loss with a mitochondrial gene mutation is highly prevalent in Japan.
    Oshima T, Ueda N, Ikeda K, Abe K, Takasaka T.
    Laryngoscope; 1999 Feb 04; 109(2 Pt 1):334-8. PubMed ID: 10890789
    [Abstract] [Full Text] [Related]

  • 18. 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 04; 28(1):49-59. PubMed ID: 18215147
    [Abstract] [Full Text] [Related]

  • 19. A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.
    Thyagarajan D, Bressman S, Bruno C, Przedborski S, Shanske S, Lynch T, Fahn S, DiMauro S.
    Ann Neurol; 2000 Nov 04; 48(5):730-6. PubMed ID: 11079536
    [Abstract] [Full Text] [Related]

  • 20. 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 Nov 04; 46(10):595-9. PubMed ID: 11587074
    [Abstract] [Full Text] [Related]

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