230 related articles for article (PubMed ID: 7603518)
1. 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]
2. 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]
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; 20(4):273-8. PubMed ID: 12903032
[TBL] [Abstract][Full Text] [Related]
4. mtDNA deletions in Kearns-Sayre.
Johns DR
Neurology; 1990 Aug; 40(8):1322-3. PubMed ID: 2381550
[No Abstract] [Full Text] [Related]
5. 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]
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; 12(1):e2328. PubMed ID: 38018320
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Mitochondrial DNA deletion and duplication in Kearns-Sayre Syndrome (KSS) with initial presentation as Pearson Marrow-Pancreas Syndrome (PMPS): Two case reports in Barranquilla, Colombia.
Sabella-Jiménez V; Otero-Herrera C; Silvera-Redondo C; Garavito-Galofre P
Mol Genet Genomic Med; 2020 Nov; 8(11):e1509. PubMed ID: 33030289
[TBL] [Abstract][Full Text] [Related]
15. Ophthalmoplegia in Mitochondrial Disease.
Lee SJ; Na JH; Han J; Lee YM
Yonsei Med J; 2018 Dec; 59(10):1190-1196. PubMed ID: 30450853
[TBL] [Abstract][Full Text] [Related]
16. Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions.
Odoardi F; Rana M; Broccolini A; Mirabella M; Modoni A; D'Amico A; Papacci M; Tonali P; Servidei S; Silvestri G
Am J Med Genet A; 2003 Apr; 118A(3):247-54. PubMed ID: 12673655
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.
Fischel-Ghodsian N; Bohlman MC; Prezant TR; Graham JM; Cederbaum SD; Edwards MJ
Pediatr Res; 1992 Jun; 31(6):557-60. PubMed ID: 1635816
[TBL] [Abstract][Full Text] [Related]
20. A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.
Schon EA; Rizzuto R; Moraes CT; Nakase H; Zeviani M; DiMauro S
Science; 1989 Apr; 244(4902):346-9. PubMed ID: 2711184
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
