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Journal Abstract Search

319 related items for PubMed ID: 18950542

  • 1. 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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  • 2. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA, Furze AD, Angeli SI.
    J Laryngol Otol; 2006 Mar; 120(3):230-2. PubMed ID: 16359140
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  • 3. 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
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  • 5. Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition.
    Sudo A, Takeichi N, Hosoki K, Saitoh S.
    J Laryngol Otol; 2011 Dec; 125(12):1282-5. PubMed ID: 21914246
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  • 6. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
    Xiu L, Zhang Q, Yu B.
    Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
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  • 7. [Maternally inherited diabetes and deafness: a case report].
    Maseda E, Sampedro A, Ablanedo A, Alonso JR.
    Acta Otorrinolaringol Esp; 2008 Nov; 59(9):472-3. PubMed ID: 19080780
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  • 11. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
    Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH.
    Ned Tijdschr Geneeskd; 1998 Jan 31; 142(5):229-33. PubMed ID: 9557035
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  • 12. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.
    Biochem Biophys Res Commun; 1998 Apr 17; 245(2):523-7. PubMed ID: 9571188
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  • 16. Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.
    Katulanda P, Groves CJ, Barrett A, Sheriff R, Matthews DR, McCarthy MI, Gloyn AL.
    Diabet Med; 2008 Mar 17; 25(3):370-4. PubMed ID: 18279408
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  • 17. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.
    Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C.
    Biochem Biophys Res Commun; 2000 Nov 02; 277(3):771-5. PubMed ID: 11062027
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