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Volumn 59, Issue 9, 2008, Pages 472-473

Maternally inherited diabetes and deafness: A case report;Síndrome de diabetes de herencia materna y sordera

Author keywords

Maternally inherited diabetes and deafness syndrome; Mitochondrial DNA; Sensorineural deafness

Indexed keywords

MITOCHONDRIAL DNA;

EID: 56049125942     PISSN: 00016519     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0001-6519(08)75121-5     Document Type: Article
Times cited : (3)

References (9)
  • 1
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    • Prevalence of mitochondrial gene mutations among hearing impaired patients
    • Usami S, Abe S, Akita J, Namba A, Shinkawa H, Ishii M, et al. Prevalence of mitochondrial gene mutations among hearing impaired patients. J Med Genet. 2000;37:38-40.
    • (2000) J Med Genet , vol.37 , pp. 38-40
    • Usami, S.1    Abe, S.2    Akita, J.3    Namba, A.4    Shinkawa, H.5    Ishii, M.6
  • 2
    • 0026849690 scopus 로고
    • Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion
    • Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koonz DA, et al. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nat Genet. 1992;1:11-5.
    • (1992) Nat Genet , vol.1 , pp. 11-15
    • Ballinger, S.W.1    Shoffner, J.M.2    Hedaya, E.V.3    Trounce, I.4    Polak, M.A.5    Koonz, D.A.6
  • 3
    • 0021143782 scopus 로고
    • Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
    • Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol. 1984;16:481-8.
    • (1984) Ann Neurol , vol.16 , pp. 481-488
    • Pavlakis, S.G.1    Phillips, P.C.2    DiMauro, S.3    De Vivo, D.C.4    Rowland, L.P.5
  • 4
    • 0038813819 scopus 로고    scopus 로고
    • Areview of cochlear implantation in mitochondrial sensorineural hearing loss
    • Sinnathuray AR, Raut V, Awa A, Magee A, Toner JG. Areview of cochlear implantation in mitochondrial sensorineural hearing loss. Otol Neurotol. 2003;24:418-26.
    • (2003) Otol Neurotol , vol.24 , pp. 418-426
    • Sinnathuray, A.R.1    Raut, V.2    Awa, A.3    Magee, A.4    Toner, J.G.5
  • 8
    • 0030021109 scopus 로고    scopus 로고
    • Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene
    • Yamasoba T, Oka Y, Tsukuda K, Nakamura M, Kaga K. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene. Laryngoscope. 1996;106:49-53.
    • (1996) Laryngoscope , vol.106 , pp. 49-53
    • Yamasoba, T.1    Oka, Y.2    Tsukuda, K.3    Nakamura, M.4    Kaga, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.