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Journal Abstract Search

139 related items for PubMed ID: 10890789

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  • 2. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
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  • 3. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
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  • 9. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.
    Remes AM, Majamaa K, Herva R, Hassinen IE.
    Neurology; 1993 May; 43(5):1015-20. PubMed ID: 8492919
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  • 11. Prevalence of mitochondrial gene mutations among hearing impaired patients.
    Usami S, Abe S, Akita J, Namba A, Shinkawa H, Ishii M, Iwasaki S, Hoshino T, Ito J, Doi K, Kubo T, Nakagawa T, Komiyama S, Tono T, Komune S.
    J Med Genet; 2000 Jan; 37(1):38-40. PubMed ID: 10633132
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  • 12. 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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  • 15. Presence of mitochondrial tRNA(Leu(UUR)) A to G 3243 mutation in DNA extracted from serum and plasma of patients with type 2 diabetes mellitus.
    Zhong S, Ng MC, Lo YM, Chan JC, Johnson PJ.
    J Clin Pathol; 2000 Jun; 53(6):466-9. PubMed ID: 10911806
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  • 17. [Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].
    Morales Angulo C, Gallo-Terán J, Señaris B, Fontalva A, González-Aguado R, Fernández-Luna JL.
    Acta Otorrinolaringol Esp; 2011 Jun; 62(2):83-6. PubMed ID: 21129708
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  • 19. Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.
    Procaccio V, Neckelmann N, Paquis-Flucklinger V, Bannwarth S, Jimenez R, Davila A, Poole JC, Wallace DC.
    Mol Diagn Ther; 2006 Jun; 10(6):381-9. PubMed ID: 17154655
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