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Journal Abstract Search

178 related items for PubMed ID: 11868597

  • 1. Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.
    Hirano M, Konishi K, Arata N, Iyori M, Saruta T, Kuramochi S, Akizuki M.
    Intern Med; 2002 Feb; 41(2):113-8. PubMed ID: 11868597
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  • 5. Hearing loss with a mitochondrial gene mutation is highly prevalent in Japan.
    Oshima T, Ueda N, Ikeda K, Abe K, Takasaka T.
    Laryngoscope; 1999 Feb; 109(2 Pt 1):334-8. PubMed ID: 10890789
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  • 6. 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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  • 7. Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation.
    Cheong HI, Chae JH, Kim JS, Park HW, Ha IS, Hwang YS, Lee HS, Choi Y.
    Pediatr Nephrol; 1999 Aug; 13(6):477-80. PubMed ID: 10452273
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  • 8. A case of mitochondrial diabetes associated with 3243 bp tRNA(Leu(UUR)) mutation with few complications, regardless of 16-year disease duration.
    Suzuki Y, Atumi Y, Matsuoka K, Taniyama M, Shigeo O.
    Diabetes Res Clin Pract; 2005 Sep; 69(3):309-10. PubMed ID: 15913828
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  • 9. 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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  • 13. [Diabetes mellitus with mitochondrial DNA tRNA(Leu)(UUR) mutation at 3256(C-T)].
    Hirai M, Suzuki S.
    Nihon Rinsho; 1998 Jan; 56 Suppl 3():530-3. PubMed ID: 9513474
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  • 14. [Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene].
    Hara K, Yamamoto M, Anegawa T, Sakuta R, Nakamura M.
    Rinsho Shinkeigaku; 1994 Apr; 34(4):361-5. PubMed ID: 8026131
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  • 16. Renal complications in patients with diabetes mellitus associated with an A to G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.
    Nakamura S, Yoshinari M, Doi Y, Yoshizumi H, Katafuchi R, Yokomizo Y, Nishiyama K, Wakisaka M, Fujishima M.
    Diabetes Res Clin Pract; 1999 Jun; 44(3):183-9. PubMed ID: 10462141
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  • 17. Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
    Gerbitz KD, Paprotta A, Jaksch M, Zierz S, Drechsel J.
    FEBS Lett; 1993 Apr 26; 321(2-3):194-6. PubMed ID: 8477849
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  • 18. Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene.
    Awata T, Matsumoto T, Iwamoto Y, Matsuda A, Kuzuya T, Saito T.
    Lancet; 1993 May 15; 341(8855):1291-2. PubMed ID: 8098444
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  • 19. Diabetes mellitus and cardiomyopathy--association with mutation in the mitochondrial tRNA(Leu)(UUR) gene.
    Shiotani H, Ueno H, Inoue S, Yokota Y, Yokoyama M.
    Jpn Circ J; 1998 Apr 15; 62(4):309-10. PubMed ID: 9583468
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  • 20. The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes.
    Karaa A, Goldstein A.
    Pediatr Diabetes; 2015 Feb 15; 16(1):1-9. PubMed ID: 25330715
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