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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

109 related items for PubMed ID: 11564302

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  • 3. 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
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  • 4. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
    Howes T, Madden C, Dasgupta S, Saeed S, Das V.
    J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
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  • 7. A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation.
    Mancuso M, Filosto M, Forli F, Rocchi A, Berrettini S, Siciliano G, Murri L.
    Acta Neurol Scand; 2004 Jul; 110(1):72-4. PubMed ID: 15180810
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  • 9. Cochlear implantation in maternal inherited diabetes and deafness syndrome.
    Raut V, Sinnathuray AR, Toner JG.
    J Laryngol Otol; 2002 May; 116(5):373-5. PubMed ID: 12080997
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  • 10. 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
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  • 11. An initial experience of cochlear implantation for patients with single-sided deafness after prior osseointegrated hearing device.
    Erbele ID, Bernstein JG, Schuchman GI, Brungart DS, Rivera A.
    Otol Neurotol; 2015 Jan; 36(1):e24-9. PubMed ID: 25406870
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  • 12. Congenital cochlear deafness in mitochondrial diseases related to RRM2B and SERAC1 gene defects. A study of the mitochondrial patients of the CMHI hospital in Warsaw, Poland.
    Iwanicka-Pronicka K, Ciara E, Piekutowska-Abramczuk D, Halat P, Pajdowska M, Pronicki M.
    Int J Pediatr Otorhinolaryngol; 2019 Jun; 121():143-149. PubMed ID: 30909120
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  • 13. [Cochlear implantation in bilateral traumatic severe to profound sensorineural deafness].
    Wang N, Xu A, Li F, Yu Y.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Apr; 50(4):324-7. PubMed ID: 26081088
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  • 15. Cochlear implantation in 13q deletion syndrome.
    Haskins A, Caten A, McKinnon BJ.
    Am J Otolaryngol; 2014 Apr; 35(1):56-8. PubMed ID: 24112761
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  • 17. [The value of genetic diagnosis of deafness in evaluating the prognosis of cochlear implantation].
    Zhang H, Chen S, Sun Y, Kong W.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Mar; 35(3):274-281. PubMed ID: 33794619
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