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Journal Abstract Search


142 related items for PubMed ID: 9266520

  • 1. Diabetes mellitus associated with 3243 mitochondrial tRNA(Leu(UUR)) mutation: clinical features and coenzyme Q10 treatment.
    Suzuki Y, Taniyama M, Muramatsu T, Atsumi Y, Hosokawa K, Asahina T, Shimada A, Murata C, Matsuoka K.
    Mol Aspects Med; 1997; 18 Suppl():S181-8. PubMed ID: 9266520
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  • 2. Mitochondrial aldehyde dehydrogenase in diabetes associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243.
    Suzuki Y, Muramatsu T, Taniyama M, Atsumi Y, Suematsu M, Kawaguchi R, Higuchi S, Asahina T, Murata C, Handa M, Matsuoka K.
    Diabetes Care; 1996 Dec; 19(12):1423-5. PubMed ID: 8941476
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  • 4. 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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  • 8. Diabetes mellitus associated with the 3243 mitochondrial tRNA(Leu)(UUR) mutation: insulin secretion and sensitivity.
    Suzuki Y, Iizuka T, Kobayashi T, Nishikawa T, Atsumi Y, Kadowaki T, Oka Y, Kadowaki H, Taniyama M, Hosokawa K, Asahina T, Matsuoka K.
    Metabolism; 1997 Sep; 46(9):1019-23. PubMed ID: 9284890
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  • 9. A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with coenzyme Q10.
    Suzuki Y, Kadowaki H, Atsumi Y, Hosokawa K, Katagiri H, Kadowaki T, Oka Y, Uyama K, Mokubo A, Asahina T.
    Endocr J; 1995 Apr; 42(2):141-5. PubMed ID: 7542975
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  • 10. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K.
    Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
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  • 11. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
    Mitsuoka T, Kawarai T, Watanabe C, Katayama S, Nakamura S.
    No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
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  • 12. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
    Tsukuda K, Suzuki Y, Kameoka K, Osawa N, Goto Y, Katagiri H, Asano T, Yazaki Y, Oka Y.
    Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930
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  • 13. Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?
    Silvestre-Aillaud P, BenDahan D, Paquis-Fluckinger V, Pouget J, Pelissier JF, Desnuelle C, Cozzone PJ, Vialettes B.
    Diabetologia; 1995 Dec; 38(12):1485-6. PubMed ID: 8786027
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  • 14. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus.
    Shigemoto M, Yoshimasa Y, Yamamoto Y, Hayashi T, Suga J, Inoue G, Okamoto M, Jingami H, Tsuda K, Yamamoto T, Yagura T, Oishi M, Tsujii S, Kuzuya H, Nakao K.
    Intern Med; 1998 Mar; 37(3):265-72. PubMed ID: 9617861
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  • 15. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ, Lertrit P, Berkovic SF, Crimmins D, Morris J, Marzuki S, Byrne E.
    Aust N Z J Med; 1994 Apr; 24(2):188-93. PubMed ID: 8042948
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  • 16. Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Kishimoto M, Hashiramoto M, Araki S, Ishida Y, Kazumi T, Kanda E, Kasuga M.
    Diabetologia; 1995 Feb; 38(2):193-200. PubMed ID: 7713314
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  • 17. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S, Hinokio Y, Ohtomo M, Hirai M, Hirai A, Chiba M, Kasuga S, Satoh Y, Akai H, Toyota T.
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
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  • 18. Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10.
    Salles JE, Moisés VA, Almeida DR, Chacra AR, Moisés RS.
    Diabetes Res Clin Pract; 2006 Apr; 72(1):100-3. PubMed ID: 16253379
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  • 19. Pancreatic exocrine dysfunction associated with mitochondrial tRNA(Leu)(UUR) mutation.
    Onishi H, Hanihara T, Sugiyama N, Kawanishi C, Iseki E, Maruyama Y, Yamada Y, Kosaka K, Yagishita S, Sekihara H, Satoh S.
    J Med Genet; 1998 Mar; 35(3):255-7. PubMed ID: 9541116
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  • 20. Mitochondrial DNA mutations in diabetes mellitus patients in Chinese Han population.
    Wang S, Wu S, Zheng T, Yang Z, Ma X, Jia W, Xiang K.
    Gene; 2013 Dec 01; 531(2):472-5. PubMed ID: 24055484
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