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Journal Abstract Search

353 related items for PubMed ID: 8896989

  • 1. Mitochondrial diabetes mellitus.
    Rötig A, Bonnefont JP, Munnich A.
    Diabetes Metab; 1996 Oct; 22(5):291-8. PubMed ID: 8896989
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  • 2. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T.
    Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824
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  • 3. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L, Wang H, Chen J, Jin W, Liu L, Ban B, Shen J, Hua Z, Chai J.
    Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
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  • 4. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
    Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC.
    Nat Genet; 1992 Apr; 1(1):11-5. PubMed ID: 1301992
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  • 5. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.
    Biochem Biophys Res Commun; 1998 Apr 17; 245(2):523-7. PubMed ID: 9571188
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  • 9. Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.
    Gómez-Zaera M, Strom TM, Rodríguez B, Estivill X, Meitinger T, Nunes V.
    Mol Genet Metab; 2001 Jan 17; 72(1):72-81. PubMed ID: 11161832
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  • 10. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
    Ohno K, Yamamoto M, Engel AG, Harper CM, Roberts LR, Tan GH, Fatourechi V.
    Ann Neurol; 1996 Jun 17; 39(6):761-6. PubMed ID: 8651648
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  • 12. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
    Maassen JA, van den Ouweland JM, t Hart LM, Lemkes HH.
    Horm Metab Res; 1997 Feb 17; 29(2):50-5. PubMed ID: 9105898
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  • 13. 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 17; 14(12):1032-7. PubMed ID: 9455930
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  • 15. Molecular and clinical aspects of mitochondrial diabetes mellitus.
    Maassen JA, van Essen E, van den Ouweland JM, Lemkes HH.
    Exp Clin Endocrinol Diabetes; 2001 Dec 17; 109(3):127-34. PubMed ID: 11409293
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  • 16. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 17; 14(6):343-8. PubMed ID: 11853367
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  • 19. Mitochondrial diseases.
    Zeviani M, Taroni F.
    Baillieres Clin Neurol; 1994 Aug 17; 3(2):315-34. PubMed ID: 7952850
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  • 20. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus.
    Małecki M, Klupa T, Wanic K, Frey J, Cyganek K, Sieradzki J.
    Med Sci Monit; 2001 Aug 17; 7(2):246-50. PubMed ID: 11257730
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