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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

511 related articles for article (PubMed ID: 2554297)

  • 1. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
    Shoffner JM; Lott MT; Voljavec AS; Soueidan SA; Costigan DA; Wallace DC
    Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7952-6. PubMed ID: 2554297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.
    Degoul F; Nelson I; Lestienne P; Francois D; Romero N; Duboc D; Eymard B; Fardeau M; Ponsot G; Paturneau-Jouas M
    J Neurol Sci; 1991 Feb; 101(2):168-77. PubMed ID: 1851820
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple short direct repeats associated with single mtDNA deletions.
    Larsson NG; Holme E
    Biochim Biophys Acta; 1992 Aug; 1139(4):311-4. PubMed ID: 1325186
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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; 309(10):403-7. PubMed ID: 2514965
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
    Mita S; Schmidt B; Schon EA; DiMauro S; Bonilla E
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9509-13. PubMed ID: 2556715
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 90(2):126-9. PubMed ID: 7484086
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome.
    Moraes CT; Schon EA; DiMauro S; Miranda AF
    Biochem Biophys Res Commun; 1989 Apr; 160(2):765-71. PubMed ID: 2541710
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.
    Larsson NG; Holme E; Kristiansson B; Oldfors A; Tulinius M
    Pediatr Res; 1990 Aug; 28(2):131-6. PubMed ID: 2395603
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Nelson I; Degoul F; Obermaier-Kusser B; Romero N; Borrone C; Marsac C; Vayssiere JL; Gerbitz K; Fardeau M; Ponsot G; Lestienne P
    Nucleic Acids Res; 1989 Oct; 17(20):8117-24. PubMed ID: 2813058
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 110(1-2):169-77. PubMed ID: 1324295
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.
    Nakase H; Moraes CT; Rizzuto R; Lombes A; DiMauro S; Schon EA
    Am J Hum Genet; 1990 Mar; 46(3):418-27. PubMed ID: 1689952
    [TBL] [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; 105(5):180-4. PubMed ID: 7630231
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 320(20):1293-9. PubMed ID: 2541333
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.
    Goto Y; Koga Y; Horai S; Nonaka I
    J Neurol Sci; 1990 Dec; 100(1-2):63-9. PubMed ID: 1965208
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
    Reichmann H; Degoul F; Gold R; Meurers B; Ketelsen UP; Hartmann J; Marsac C; Lestienne P
    Eur Neurol; 1991; 31(2):108-13. PubMed ID: 1646110
    [TBL] [Abstract][Full Text] [Related]  

  • 16. mtDNA deletions in Kearns-Sayre.
    Johns DR
    Neurology; 1990 Aug; 40(8):1322-3. PubMed ID: 2381550
    [No Abstract]   [Full Text] [Related]  

  • 17. 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; 123(1-2):140-6. PubMed ID: 8064307
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies.
    Gerbitz KD; Obermaier-Kusser B; Lestienne P; Zierz S; Müller-Höcker J; Pongratz D; Paetzke-Brunner I; Deufel T
    J Clin Chem Clin Biochem; 1990 Apr; 28(4):241-50. PubMed ID: 2162908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].
    Desnuelle C; Pellissier JF; Serratrice G; Pouget J; Turnbull DM
    Rev Neurol (Paris); 1989; 145(12):842-50. PubMed ID: 2559448
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Kearns-Sayre syndrome with muscle mitochondrial DNA deletion.
    Lestienne P; Ponsot G
    Lancet; 1988 Apr; 1(8590):885. PubMed ID: 2895391
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 26.