These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

178 related items for PubMed ID: 9197460

  • 1. Quantitative analysis of mitochondrial DNA deletion in paraffin embedded muscle tissues from patients with KSS and CPEO.
    Kim SH, Chi JG, Reith A, Kadenbach B.
    Biochim Biophys Acta; 1997 May 24; 1360(3):193-5. PubMed ID: 9197460
    [Abstract] [Full Text] [Related]

  • 2. [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 24; 20(4):273-8. PubMed ID: 12903032
    [Abstract] [Full Text] [Related]

  • 3. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
    Poulton J, Morten KJ, Weber K, Brown GK, Bindoff L.
    Hum Mol Genet; 1994 Jun 24; 3(6):947-51. PubMed ID: 7951243
    [Abstract] [Full Text] [Related]

  • 4. CPEO and KSS differ in the percentage and location of the mtDNA deletion.
    López-Gallardo E, López-Pérez MJ, Montoya J, Ruiz-Pesini E.
    Mitochondrion; 2009 Sep 24; 9(5):314-7. PubMed ID: 19410662
    [Abstract] [Full Text] [Related]

  • 5. Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.
    Fassati A, Bordoni A, Amboni P, Fortunato F, Fagiolari G, Bresolin N, Prelle A, Comi G, Scarlato G.
    J Neurol Sci; 1994 May 24; 123(1-2):140-6. PubMed ID: 8064307
    [Abstract] [Full Text] [Related]

  • 6. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y, Hou Y, Zhao X, Liufu T, Yu M, Zhang W, Xie Z, Zhang VW, Yuan Y, Wang Z.
    Mol Genet Genomic Med; 2024 Jan 24; 12(1):e2328. PubMed ID: 38018320
    [Abstract] [Full Text] [Related]

  • 7. A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletion.
    Coulter-Mackie MB, Applegarth DA, Toone JR, Gagnier L.
    Clin Biochem; 1998 Nov 24; 31(8):627-32. PubMed ID: 9876894
    [Abstract] [Full Text] [Related]

  • 8. A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples.
    De Coo IF, Gussinklo T, Arts PJ, Van Oost BA, Smeets HJ.
    J Neurol Sci; 1997 Jul 24; 149(1):37-40. PubMed ID: 9168163
    [Abstract] [Full Text] [Related]

  • 9. [Chronic progressive external ophthalmoplegia (CPEO), Kearns-Sayre syndrome (KSS)].
    Ishikawa H, Nishino I.
    Ryoikibetsu Shokogun Shirizu; 2001 Jul 24; (36):153-6. PubMed ID: 11596351
    [No Abstract] [Full Text] [Related]

  • 10. Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Bosbach S, Kornblum C, Schröder R, Wagner M.
    Brain; 2003 May 24; 126(Pt 5):1231-40. PubMed ID: 12690061
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia.
    Kiyomoto BH, Tengan CH, Moraes CT, Oliveira AS, Gabbai AA.
    J Neurol Sci; 1997 Nov 25; 152(2):160-5. PubMed ID: 9415537
    [Abstract] [Full Text] [Related]

  • 12. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
    Barrientos A, Casademont J, Grau JM, Cardellach F, Montoya J, Estivill X, Urbano-Márquez A, Nunes V.
    Med Clin (Barc); 1995 Jul 01; 105(5):180-4. PubMed ID: 7630231
    [Abstract] [Full Text] [Related]

  • 13. Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation.
    Kierdaszuk B, Kaliszewska M, Rusecka J, Kosińska J, Bartnik E, Tońska K, Kamińska AM, Kostera-Pruszczyk A.
    Genes (Basel); 2020 Dec 31; 12(1):. PubMed ID: 33396418
    [Abstract] [Full Text] [Related]

  • 14. Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes.
    Sadikovic B, Wang J, El-Hattab AW, Landsverk M, Douglas G, Brundage EK, Craigen WJ, Schmitt ES, Wong LJ.
    PLoS One; 2010 Dec 20; 5(12):e15687. PubMed ID: 21187929
    [Abstract] [Full Text] [Related]

  • 15. [Partial deletion of mitochondrial DNA in mitochondrial encephalomyopathies].
    Wang W, Zhang J, Guo Y, Guo Z, Ren H.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1997 Aug 20; 19(4):278-83. PubMed ID: 10453567
    [Abstract] [Full Text] [Related]

  • 16. [A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].
    Akaike M, Kawai H, Kashiwagi S, Kunishige M, Saito S.
    Rinsho Shinkeigaku; 1995 Feb 20; 35(2):190-4. PubMed ID: 7781238
    [Abstract] [Full Text] [Related]

  • 17. Characterization of a mitochondrial DNA deletion in patients with mitochondrial myopathy.
    Kim SH, Chi JG.
    Mol Cells; 1997 Dec 31; 7(6):726-9. PubMed ID: 9509412
    [Abstract] [Full Text] [Related]

  • 18. [Single deletion of mitochondrial DNA: CPEO, Kearns-Sayre syndrome].
    Arisato T, Higuchi I, Nakagawa M.
    Nihon Rinsho; 2002 Apr 31; 60 Suppl 4():458-61. PubMed ID: 12013912
    [No Abstract] [Full Text] [Related]

  • 19. Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
    Grigalionienė K, Burnytė B, Balkelienė D, Ambrozaitytė L, Utkus A.
    Mol Genet Genomic Med; 2023 Jan 31; 11(1):e2059. PubMed ID: 36181358
    [Abstract] [Full Text] [Related]

  • 20. Clinical Phenotype and Genetic Features of a Pair of Chinese Twins with Kearns-Sayre Syndrome.
    Guo L, Wang X, Ji H.
    DNA Cell Biol; 2020 Aug 31; 39(8):1449-1457. PubMed ID: 32609007
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.