BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 2381550)

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

  • 2. Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
    Poulton J; Morten KJ; Marchington D; Weber K; Brown GK; Rötig A; Bindoff L
    Muscle Nerve Suppl; 1995; 3():S154-8. PubMed ID: 7603518
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathy.
    Kosmorsky G; Johns DR
    Neurol Clin; 1991 Feb; 9(1):147-61. PubMed ID: 2011107
    [No Abstract]   [Full Text] [Related]  

  • 8. [Ophthalmoplegia-plus: clinical variability, biochemical defects of the mitochondria respiratory chain and deletions of the mitochondria genome].
    Zierz S; von Wersebe O; Gerbitz KD; Jerusalem F
    Nervenarzt; 1990 Jun; 61(6):332-9. PubMed ID: 2377259
    [No Abstract]   [Full Text] [Related]  

  • 9. [PCR-based detection of heteroplasmic deleted mitochondrial DNA in Kearns-Sayre syndrome].
    Ramírez-Miranda A; Navas-Pérez A; Gurria-Quintana L; Vargas-Ortega J; Murillo-Correa C; Zenteno JC
    Arch Soc Esp Oftalmol; 2008 Mar; 83(3):155-9. PubMed ID: 18311673
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
    Zeviani M; Moraes CT; DiMauro S; Nakase H; Bonilla E; Schon EA; Rowland LP
    Neurology; 1988 Sep; 38(9):1339-46. PubMed ID: 3412580
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A patient with Pearson and Kearns-Sayre syndrome and a common 4.9 Kb deletion of mitochondrial DNA in blood].
    Guirado Giménez F; Montoya Villarroya J; Oliván del Cacho MJ; Playán Ariso A; Alcaine Villarroya MJ; Rábano Rodríguez A; Baldellou Vázquez A; López-Pisón J
    An Esp Pediatr; 1998 Nov; 49(5):510-2. PubMed ID: 9949596
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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; 3(6):947-51. PubMed ID: 7951243
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes.
    Gerbitz KD; Obermaier-Kusser B; Zierz S; Pongratz D; Müller-Höcker J; Lestienne P
    J Neurol; 1990 Feb; 237(1):5-10. PubMed ID: 2156958
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.