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Journal Abstract Search

637 related items for PubMed ID: 16788417

  • 1. 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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  • 2. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
    Newkirk JE, Taylor RW, Howell N, Bindoff LA, Chinnery PF, Alberti KG, Turnbull DM, Walker M.
    Diabet Med; 1997 Jun; 14(6):457-60. PubMed ID: 9212310
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  • 3. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
    van den Ouweland JM, Lemkes HH, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PA, van de Kamp JJ, Maassen JA.
    Nat Genet; 1992 Aug; 1(5):368-71. PubMed ID: 1284550
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  • 4. Audiological findings of sensorineural deafness associated with a mutation in the mitochondrial DNA.
    Sawada S, Takeda T, Kakigi A, Saito H, Suehiro T, Nakauchi Y, Chikamori K.
    Am J Otol; 1997 May; 18(3):332-5. PubMed ID: 9149827
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  • 7. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].
    Biarnés J, Barrientos A, Ricart W, Nunes V, Fernández-Castañer M, Soler J.
    Med Clin (Barc); 1999 Jan 30; 112(3):99-101. PubMed ID: 10074618
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  • 9. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 30; 14(6):343-8. PubMed ID: 11853367
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  • 10. [Maternally inherited diabetes and deafness: a case report].
    Maseda E, Sampedro A, Ablanedo A, Alonso JR.
    Acta Otorrinolaringol Esp; 2008 Nov 30; 59(9):472-3. PubMed ID: 19080780
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  • 11. 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 30; 130(3):281-8. PubMed ID: 15023833
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  • 12. Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9.
    Bom SJ, Kemperman MH, De Kok YJ, Huygen PL, Verhagen WI, Cremers FP, Cremers CW.
    Laryngoscope; 1999 Sep 30; 109(9):1525-30. PubMed ID: 10499067
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  • 14. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?
    Holmes-Walker DJ, Mitchell P, Boyages SC.
    Diabet Med; 1998 Nov 30; 15(11):946-52. PubMed ID: 9827849
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  • 17. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
    Xiu L, Zhang Q, Yu B.
    Zhonghua Yi Xue Za Zhi; 1997 Jun 30; 77(6):418-21. PubMed ID: 9772504
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  • 20. 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 30; 129(4):421-6. PubMed ID: 12707188
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