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Journal Abstract Search

169 related items for PubMed ID: 1591103

  • 1. [MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].
    Onishi H, Inoue K, Osaka H, Nagatomo H, Ando N, Yamada Y, Suzuki K, Hanihara T, Kawamoto S, Okuda K.
    No To Shinkei; 1992 Mar; 44(3):259-64. PubMed ID: 1591103
    [Abstract] [Full Text] [Related]

  • 2. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML, Moraes CT, Shanske S, Langman CB, Ciafaloni E, DiMauro S.
    Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371
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  • 3. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
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  • 4. 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; 39(6):761-6. PubMed ID: 8651648
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  • 5. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M.
    Cas Lek Cesk; 1998 Jul 13; 137(14):430-3. PubMed ID: 9748738
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  • 7. [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 13; 34(4):361-5. PubMed ID: 8026131
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  • 9. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov 13; 110(11):851-5. PubMed ID: 9772417
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  • 10. A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy.
    Goto Y, Tojo M, Tohyama J, Horai S, Nonaka I.
    Ann Neurol; 1992 Jun 13; 31(6):672-5. PubMed ID: 1514779
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  • 11. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Hess JF, Parisi MA, Bennett JL, Clayton DA.
    Nature; 1991 May 16; 351(6323):236-9. PubMed ID: 1755869
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  • 12. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
    Song D, Zhang Y, Shi J, Lü Q, Chen J, Zhang H, Zhang W, Wang H, Cai Q.
    Chin Med J (Engl); 2001 Dec 16; 114(12):1273-5. PubMed ID: 11793851
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  • 14. [Mitochondrial diabetes complicated by or associated with "MELAS" syndrome?].
    Drouet A, Guilloton L, Godinot C, Rochet D, Ribot C, Carrier H.
    Rev Neurol (Paris); 2000 Oct 16; 156(10):892-5. PubMed ID: 11033519
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  • 16. 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 16; 113(2):111-6. PubMed ID: 11775531
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  • 19. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N, Babazono T, Tsuchiya K, Tomonaga O, Suzuki A, Togashi M, Ujihara N, Sakka Y, Yokokawa H, Ogata M, Nihei H, Iwamoto Y.
    J Hum Genet; 2001 Feb 16; 46(6):330-4. PubMed ID: 11393536
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  • 20. [A case of MELAS presenting juvenile-onset hyperglycemic chorea-ballism].
    Nakagaki H, Furuya J, Santa Y, Nagano S, Araki E, Yamada T.
    Rinsho Shinkeigaku; 2005 Jul 16; 45(7):502-5. PubMed ID: 16119832
    [Abstract] [Full Text] [Related]

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