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528 related items for PubMed ID: 8651648

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T.
    Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
    Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 6. 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 13; 29(6):680-3. PubMed ID: 1892371
    [Abstract] [Full Text] [Related]

  • 7. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb 13; 27(1):77-80. PubMed ID: 15782498
    [Abstract] [Full Text] [Related]

  • 8. Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.
    Wang Z, Liu S, Yang Y, Yuan Y, Wu L, Qi Y, Chen Q.
    Chin Med J (Engl); 2002 Jul 13; 115(7):995-7. PubMed ID: 12150728
    [Abstract] [Full Text] [Related]

  • 9. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ.
    Brain Dev; 2004 Oct 13; 26(7):459-62. PubMed ID: 15351082
    [Abstract] [Full Text] [Related]

  • 10. Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies.
    Bonod-Bidaud C, Giraud S, Mandon G, Mousson B, Stepien G.
    Exp Cell Res; 1999 Jan 10; 246(1):91-7. PubMed ID: 9882518
    [Abstract] [Full Text] [Related]

  • 11. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW, Huang CC, Tsai JL, Liu JY, Pang CY, Lee HC, Wang EK, Wei YH.
    Acta Neurol Scand; 2000 Jan 10; 101(1):65-9. PubMed ID: 10660156
    [Abstract] [Full Text] [Related]

  • 12. A case of Kearns-Sayre syndrome with the 4,977-bp common deletion associated with a novel 7,704-bp deletion.
    Vázquez-Acevedo M, Vázquez-Memije ME, Mutchinick OM, Morales JJ, García-Ramos G, González-Halphen D.
    Neurol Sci; 2002 Dec 10; 23(5):247-50. PubMed ID: 12522683
    [Abstract] [Full Text] [Related]

  • 13. [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 10; 44(3):259-64. PubMed ID: 1591103
    [Abstract] [Full Text] [Related]

  • 14. A case of Kearns-Sayre syndrome with autoimmune thyroiditis and possible Hashimoto encephalopathy.
    Berio A, Piazzi A.
    Panminerva Med; 2002 Sep 10; 44(3):265-9. PubMed ID: 12094144
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial genome analysis in Kearns-Sayre syndrome.
    Lertrit P, Atchaneeyasakul L, Devahastin V, Saechan V, Sangruchi T, Neungton N, Lekhakula S.
    Southeast Asian J Trop Med Public Health; 1995 Sep 10; 26 Suppl 1():162-5. PubMed ID: 8629098
    [Abstract] [Full Text] [Related]

  • 16. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH.
    Acta Neurol Scand; 2006 May 10; 113(5):334-41. PubMed ID: 16629770
    [Abstract] [Full Text] [Related]

  • 17. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
    Degoul F, Diry M, Pou-Serradell A, Lloreta J, Marsac C.
    Ann Neurol; 1994 Mar 10; 35(3):365-70. PubMed ID: 8122891
    [Abstract] [Full Text] [Related]

  • 18. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].
    Capková M, Tesarová M, Wenchich L, Cerná L, Hansíková H, Hůlková H, Hrubá E, Elleder M, Zeman J.
    Cas Lek Cesk; 2002 Feb 01; 141(2):51-4. PubMed ID: 11925663
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct 01; 5(5):622-32. PubMed ID: 1392136
    [Abstract] [Full Text] [Related]

  • 20. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
    Delgado-Sánchez R, Zárate-Moysen A, Monsalvo-Reyes A, Herrero MD, Ruiz-Pesini E, López-Pérez M, Montoya J, Montiel-Sosa JF.
    Rev Neurol; 1992 Oct 01; 44(1):18-22. PubMed ID: 17199225
    [Abstract] [Full Text] [Related]

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