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

332 related items for PubMed ID: 18340555

  • 41. Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafness.
    Bathelier C, François M, Lucotte G.
    Genet Couns; 2004; 15(1):61-6. PubMed ID: 15083701
    [Abstract] [Full Text] [Related]

  • 42. Despite a lack of otoacoustic emission, word recognition is not seriously influenced in a TECTA DFNA8/12 family.
    Ramsebner R, Koenighofer M, Parzefall T, Lucas T, Schoefer C, Frei K.
    Int J Pediatr Otorhinolaryngol; 2014 May; 78(5):837-42. PubMed ID: 24636747
    [Abstract] [Full Text] [Related]

  • 43. 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; 109(2 Pt 1):334-8. PubMed ID: 10890789
    [Abstract] [Full Text] [Related]

  • 44. 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]

  • 45. 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]

  • 46. 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]

  • 47. Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Jun 16; 344(4):1253-7. PubMed ID: 16650816
    [Abstract] [Full Text] [Related]

  • 48. Mitochondrial syndromic sensorineural hearing loss.
    Forli F, Passetti S, Mancuso M, Seccia V, Siciliano G, Nesti C, Berrettini S.
    Biosci Rep; 2007 Jun 16; 27(1-3):113-23. PubMed ID: 17487579
    [Abstract] [Full Text] [Related]

  • 49. [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 16; 45(7):982-91. PubMed ID: 19705751
    [Abstract] [Full Text] [Related]

  • 50. Distortion-product otoacoustic emission tests evaluate cochlear function and differentiate cochlear and vestibular schwannoma.
    Kagoya R, Shinogami M, Kohno M, Yamasoba T.
    Otolaryngol Head Neck Surg; 2013 Feb 16; 148(2):267-71. PubMed ID: 23197675
    [Abstract] [Full Text] [Related]

  • 51. Confirmation of PDZD7 as a Nonsyndromic Hearing Loss Gene.
    Vona B, Lechno S, Hofrichter MA, Hopf S, Läig AK, Haaf T, Keilmann A, Zechner U, Bartsch O.
    Ear Hear; 2016 Feb 16; 37(4):e238-46. PubMed ID: 26849169
    [Abstract] [Full Text] [Related]

  • 52. [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]

  • 53. The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers.
    Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, Barges S, Pratt H.
    Hear Res; 2002 Jan 30; 163(1-2):93-100. PubMed ID: 11788203
    [Abstract] [Full Text] [Related]

  • 54. Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.
    Huang T, Santarelli R, Starr A.
    Brain Res; 2009 Dec 01; 1300():97-104. PubMed ID: 19733158
    [Abstract] [Full Text] [Related]

  • 55. Auditory neuropathy in childhood.
    Doyle KJ, Sininger Y, Starr A.
    Laryngoscope; 1998 Sep 01; 108(9):1374-7. PubMed ID: 9738760
    [Abstract] [Full Text] [Related]

  • 56. [Audiological test results of the autoimmune sensorineural hearing loss].
    Gu R, Zou J, Yu L.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1995 Sep 01; 30(1):20-3. PubMed ID: 7598979
    [Abstract] [Full Text] [Related]

  • 57. A review of cochlear implantation in mitochondrial sensorineural hearing loss.
    Sinnathuray AR, Raut V, Awa A, Magee A, Toner JG.
    Otol Neurotol; 2003 May 01; 24(3):418-26. PubMed ID: 12806294
    [Abstract] [Full Text] [Related]

  • 58. 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 01; 73(1):50-4. PubMed ID: 18028453
    [Abstract] [Full Text] [Related]

  • 59. [A case of preserved otoacoustic emissions in a child with unilateral idiopathic severe sensorineural hearing loss].
    Namysłowski G, Morawski K, Trybalska G.
    Otolaryngol Pol; 1999 Jan 01; 53(1):101-5. PubMed ID: 10337167
    [Abstract] [Full Text] [Related]

  • 60. Successful cochlear implantation in two profoundly deafened patients with neurofibromatosis type 1: further evidence to support a cochlear site of lesion.
    Vincenti V, Pasanisi E, Guida M, Di Lella F, Giordano D, Bacciu A.
    Otol Neurotol; 2015 Apr 01; 36(4):588-91. PubMed ID: 25356763
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 17.