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Journal Abstract Search

190 related items for PubMed ID: 2375642

  • 1. Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.
    Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S.
    Ann Neurol; 1990 Jul; 28(1):94-7. PubMed ID: 2375642
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S.
    N Engl J Med; 1989 May 18; 320(20):1293-9. PubMed ID: 2541333
    [Abstract] [Full Text] [Related]

  • 3. [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 18; 20(4):273-8. PubMed ID: 12903032
    [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. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ, Lopez Gallardo E, Solano A, Dahmani Y, Herrero MD, Montoya J.
    Neurologia; 2006 Sep 01; 21(7):357-64. PubMed ID: 16977556
    [Abstract] [Full Text] [Related]

  • 6. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
    Moslemi AR, Melberg A, Holme E, Oldfors A.
    Ann Neurol; 1996 Nov 01; 40(5):707-13. PubMed ID: 8957011
    [Abstract] [Full Text] [Related]

  • 7. Deletion screening of mitochondrial DNA via multiprimer DNA amplification.
    Ernst BP, Wilichowski E, Wagner M, Hanefeld F.
    Mol Cell Probes; 1994 Feb 01; 8(1):45-9. PubMed ID: 8028607
    [Abstract] [Full Text] [Related]

  • 8. [Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].
    Nelson I, d'Auriol L, Galibert F, Ponsot G, Lestienne P.
    C R Acad Sci III; 1989 Feb 01; 309(10):403-7. PubMed ID: 2514965
    [Abstract] [Full Text] [Related]

  • 9. Widespread tissue distribution of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.
    Kawashima S, Ohta S, Kagawa Y, Yoshida M, Nishizawa M.
    Muscle Nerve; 1994 Jul 01; 17(7):741-6. PubMed ID: 8008000
    [Abstract] [Full Text] [Related]

  • 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 01; 39(6):761-6. PubMed ID: 8651648
    [Abstract] [Full Text] [Related]

  • 11. Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations.
    Nelson I, Bonne G, Degoul F, Marsac C, Ponsot G, Lestienne P.
    Neuropediatrics; 1992 Aug 01; 23(4):199-205. PubMed ID: 1407387
    [Abstract] [Full Text] [Related]

  • 12. Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Ota Y, Tanaka M, Sato W, Ohno K, Yamamoto T, Maehara M, Negoro T, Watanabe K, Awaya S, Ozawa T.
    Invest Ophthalmol Vis Sci; 1991 Sep 01; 32(10):2667-75. PubMed ID: 1894466
    [Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution.
    Poulton J, Deadman ME, Gardiner RM.
    Nucleic Acids Res; 1989 Dec 25; 17(24):10223-9. PubMed ID: 2602151
    [Abstract] [Full Text] [Related]

  • 15. 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 25; 31(8):627-32. PubMed ID: 9876894
    [Abstract] [Full Text] [Related]

  • 16. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.
    Brockington M, Sweeney MG, Hammans SR, Morgan-Hughes JA, Harding AE.
    Nat Genet; 1993 May 25; 4(1):67-71. PubMed ID: 8513327
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