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Journal Abstract Search

156 related items for PubMed ID: 9003302

  • 1. Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathies.
    Collombet JM, Mandon G, Dumoulin R, Mousson B, Stepien G.
    Mol Gen Genet; 1996 Nov 27; 253(1-2):182-8. PubMed ID: 9003302
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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 25; 123(1-2):140-6. PubMed ID: 8064307
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5. New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle.
    Schröder R, Vielhaber S, Wiedemann FR, Kornblum C, Papassotiropoulos A, Broich P, Zierz S, Elger CE, Reichmann H, Seibel P, Klockgether T, Kunz WS.
    J Neuropathol Exp Neurol; 2000 May 01; 59(5):353-60. PubMed ID: 10888364
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy.
    Marzuki S, Berkovic SF, Saifuddin Noer A, Kapsa RM, Kalnins RM, Byrne E, Sasmono T, Sudoyo H.
    J Neurol Sci; 1997 Feb 12; 145(2):155-62. PubMed ID: 9094043
    [Abstract] [Full Text] [Related]

  • 9. Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe.
    Nakamura N, Hattori N, Tanaka M, Mizuno Y.
    Biochim Biophys Acta; 1996 Sep 11; 1308(3):215-21. PubMed ID: 8809113
    [Abstract] [Full Text] [Related]

  • 10. 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 11; 12(1):e2328. PubMed ID: 38018320
    [Abstract] [Full Text] [Related]

  • 11. 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 11; 149(1):37-40. PubMed ID: 9168163
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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 May 24; 26 Suppl 1():162-5. PubMed ID: 8629098
    [Abstract] [Full Text] [Related]

  • 14. [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]

  • 15. 3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.
    Klopstock T, Bischof F, Gerok K, Deuschl G, Seibel P, Ketelsen UP, Reichmann H.
    Acta Neuropathol; 1995 Aug 24; 90(2):126-9. PubMed ID: 7484086
    [Abstract] [Full Text] [Related]

  • 16. Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patients.
    Laforêt P, Lombès A, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M.
    Neuromuscul Disord; 1995 Sep 24; 5(5):399-413. PubMed ID: 7496174
    [Abstract] [Full Text] [Related]

  • 17. [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 24; 19(4):278-83. PubMed ID: 10453567
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M.
    J Neurol Sci; 1992 Jul 31; 110(1-2):169-77. PubMed ID: 1324295
    [Abstract] [Full Text] [Related]

  • 20. Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia.
    Rodríguez-López C, García-Cárdaba LM, Blázquez A, Serrano-Lorenzo P, Gutiérrez-Gutiérrez G, San Millán-Tejado B, Muelas N, Hernández-Laín A, Vílchez JJ, Gutiérrez-Rivas E, Arenas J, Martín MA, Domínguez-González C.
    J Med Genet; 2020 Sep 31; 57(9):643-646. PubMed ID: 32161153
    [Abstract] [Full Text] [Related]

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