메뉴 건너뛰기




Volumn 122, Issue 11, 2008, Pages 1249-1252

Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome

Author keywords

Cochlear implantation; Heteroplasmy; MIDD; Mitochondrial DNA; Sensorineural hearing loss

Indexed keywords

MITOCHONDRIAL DNA;

EID: 54949131798     PISSN: 00222151     EISSN: 17485460     Source Type: Journal    
DOI: 10.1017/S0022215108001503     Document Type: Article
Times cited : (8)

References (18)
  • 1
    • 0029888826 scopus 로고    scopus 로고
    • Measuring patient benefit from otorhinolaryngological surgery and therapy
    • Robinson K, Gatehouse S, Browning G. Measuring patient benefit from otorhinolaryngological surgery and therapy. Ann Otol Rhinol Laryngol 1996;105:415-22
    • (1996) Ann Otol Rhinol Laryngol , vol.105 , pp. 415-422
    • Robinson, K.1    Gatehouse, S.2    Browning, G.3
  • 3
    • 0032231623 scopus 로고    scopus 로고
    • Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: Prevalence of the mutation in an adult population
    • Majamaa K, Moilanen JS, Uimonen S, Remes AM, Salmela PI, Karppa M et al. Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population. Am J Hum Genet 1998;63:447-54
    • (1998) Am J Hum Genet , vol.63 , pp. 447-454
    • Majamaa, K.1    Moilanen, J.S.2    Uimonen, S.3    Remes, A.M.4    Salmela, P.I.5    Karppa, M.6
  • 4
    • 0034054301 scopus 로고    scopus 로고
    • 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
  • 5
    • 0034758460 scopus 로고    scopus 로고
    • Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics
    • Nagata H, Kunahara K, Tomemori T, Arimoto Y, Isoyama K, Yoshida K et al. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics. J Hum Genet 2001;46:595-9
    • (2001) J Hum Genet , vol.46 , pp. 595-599
    • Nagata, H.1    Kunahara, K.2    Tomemori, T.3    Arimoto, Y.4    Isoyama, K.5    Yoshida, K.6
  • 6
    • 0025666322 scopus 로고
    • leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
    • leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 1990;348:651-3
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 8
    • 0035016350 scopus 로고    scopus 로고
    • Hearing impairment in patients with 3243 A>G mtDNA mutation: Phenotype and rate of progression
    • Uimonen S, Moilanen JS, Sorri M, Hassinen IE, Majamaa K. Hearing impairment in patients with 3243 A>G mtDNA mutation: phenotype and rate of progression. Hum Genet 2001;108:284-9
    • (2001) Hum Genet , vol.108 , pp. 284-289
    • Uimonen, S.1    Moilanen, J.S.2    Sorri, M.3    Hassinen, I.E.4    Majamaa, K.5
  • 11
    • 0030059395 scopus 로고    scopus 로고
    • Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome
    • Oshima T, Ueda N, Ikeda K, Abe K, Takasaka T. Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome. Laryngoscope 1996;106:43-8
    • (1996) Laryngoscope , vol.106 , pp. 43-48
    • Oshima, T.1    Ueda, N.2    Ikeda, K.3    Abe, K.4    Takasaka, T.5
  • 13
    • 0028022596 scopus 로고
    • A molecular and cellular hypothesis for aminoglycoside-induced deafness
    • Cortopassi G, Hutchin T. A molecular and cellular hypothesis for aminoglycoside-induced deafness. Hear Res 1994;78:27-30
    • (1994) Hear Res , vol.78 , pp. 27-30
    • Cortopassi, G.1    Hutchin, T.2
  • 15
    • 0027318529 scopus 로고
    • Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(VVR)) mutation
    • Remes AM, Majamaa K, Herva R, Hassinen IE. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(VVR)) mutation. Neurology 1993;35:1015-20
    • (1993) Neurology , vol.35 , pp. 1015-1020
    • Remes, A.M.1    Majamaa, K.2    Herva, R.3    Hassinen, I.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.