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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

226 related items for PubMed ID: 19893302

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  • 3. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS, Brown DJ, McMillan PM, Barker SE, Lesperance MM.
    Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340
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  • 4. Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis.
    Oonk AM, Leijendeckers JM, Lammers EM, Weegerink NJ, Oostrik J, Beynon AJ, Huygen PL, Kunst HP, Kremer H, Snik AF, Pennings RJ.
    Hear Res; 2013 May; 299():88-98. PubMed ID: 23340379
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  • 7. 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; 28(1):49-59. PubMed ID: 18215147
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  • 8. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 11. Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
    Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 2003 Apr; 129(4):421-6. PubMed ID: 12707188
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  • 15. [Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].
    Jin Z, Cheng J, Lu Y, Li J, Sun Y, Yuan H, Han D.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Feb; 25(4):158-61. PubMed ID: 21563462
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  • 16. A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study.
    Kim BJ, Han JH, Park HR, Kim MY, Kim AR, Oh SH, Park WY, Oh DY, Lee S, Choi BY.
    J Gene Med; 2018 Jun; 20(6):e3019. PubMed ID: 29607572
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  • 17. A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.
    Kemperman MH, De Leenheer EM, Huygen PL, van Wijk E, van Duijnhoven G, Cremers FP, Kremer H, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 2004 Mar; 130(3):281-8. PubMed ID: 15023833
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  • 18. Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.
    Payne M, Yang Z, Katz BJ, Warner JE, Weight CJ, Zhao Y, Pearson ED, Treft RL, Hillman T, Kennedy RJ, Meire FM, Zhang K.
    Am J Ophthalmol; 2004 Nov; 138(5):749-55. PubMed ID: 15531309
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  • 19. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area].
    Oeken J, König E.
    HNO; 1993 Jun; 41(6):301-10. PubMed ID: 8365917
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  • 20. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
    Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.
    Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963
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