221 related articles for article (PubMed ID: 11245066)
1. Mitochondrial gene defect in patients with chronic progressive external ophthalmoplegia.
Chen Q; Li X; Wu L; Qi Y; Wu X
Chin Med J (Engl); 1998 Jun; 111(6):500-3. PubMed ID: 11245066
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [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; 19(4):278-83. PubMed ID: 10453567
[TBL] [Abstract][Full Text] [Related]
4. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
Kornblum C; Zsurka G; Wiesner RJ; Schröder R; Kunz WS
Biosci Rep; 2008 Apr; 28(2):89-96. PubMed ID: 18384291
[TBL] [Abstract][Full Text] [Related]
5. A novel heteroplasmic tRNA(Leu(CUN)) mtDNA point mutation associated with chronic progressive external ophthalmoplegia.
Cardaioli E; Da Pozzo P; Radi E; Dotti MT; Federico A
Biochem Biophys Res Commun; 2005 Feb; 327(3):675-8. PubMed ID: 15649400
[TBL] [Abstract][Full Text] [Related]
6. The molecular genetics of mitochondrial cytopathies: the Melbourne experience.
Thyagarajan D; Byrne E; Dennet X; Marzuki S
Clin Exp Neurol; 1992; 29():172-81. PubMed ID: 1343860
[TBL] [Abstract][Full Text] [Related]
7. [Multiple mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO)].
Kawashima S; Nishizawa M
Nihon Rinsho; 1993 Sep; 51(9):2391-5. PubMed ID: 8411718
[TBL] [Abstract][Full Text] [Related]
8. Abnormal H-Tfam in a patient harboring a single mtDNA deletion.
Tessa A; Manca ML; Mancuso M; Renna MR; Murri L; Martini B; Santorelli FM; Siciliano G
Funct Neurol; 2000; 15(4):211-4. PubMed ID: 11213524
[TBL] [Abstract][Full Text] [Related]
9. Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations.
Kollberg G; Jansson M; Pérez-Bercoff A; Melberg A; Lindberg C; Holme E; Moslemi AR; Oldfors A
Eur J Hum Genet; 2005 Apr; 13(4):463-9. PubMed ID: 15702133
[TBL] [Abstract][Full Text] [Related]
10. [Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)].
Kornblum C; Kunz WS; Klockgether T; Roggenkämper P; Schröder R
Klin Monbl Augenheilkd; 2004 Dec; 221(12):1057-61. PubMed ID: 15599814
[TBL] [Abstract][Full Text] [Related]
11. A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.
Cardaioli E; Da Pozzo P; Gallus GN; Malandrini A; Gambelli S; Gaudiano C; Malfatti E; Viscomi C; Zicari E; Berti G; Serni G; Dotti MT; Federico A
Neuromuscul Disord; 2007 Oct; 17(9-10):681-3. PubMed ID: 17614276
[TBL] [Abstract][Full Text] [Related]
12. [Molecular studies in Cuban patients with progressive external ophthalmoplegia].
Rodríguez-Hernández M; Hirano M; Arrieta T; Lestayo Z; Estrada R; Santiesteban R; Guerra-Badía R; Galarraga J; Gutierres J; Hechevarría E; Andreu A; Montoya J; DiMauro S
Rev Neurol; 2000 Jun 1-15; 30(11):1001-5. PubMed ID: 10904941
[TBL] [Abstract][Full Text] [Related]
13. Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia.
Ville-Ferlin T; Dumoulin R; Stepien G; Matha V; Bady B; Flocard F; Carrier H; Mathieu M; Mousson B
Mol Cell Probes; 1995 Jun; 9(3):207-14. PubMed ID: 7477015
[TBL] [Abstract][Full Text] [Related]
14. Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNA.
Cardaioli E; Da Pozzo P; Malfatti E; Gallus GN; Rubegni A; Malandrini A; Gaudiano C; Guidi L; Serni G; Berti G; Dotti MT; Federico A
J Neurol Sci; 2008 Sep; 272(1-2):106-9. PubMed ID: 18603265
[TBL] [Abstract][Full Text] [Related]
15. [A single deletion of mitochondrial DNA in a Brazilian patient with chronic progressive external ophthalmoplegia].
Carod-Artal FJ; Solano-Palacios A; Playán-Ariso A; Viana-Brandi I; López-Gallardo E; Andreu A; López-Pérez M; Montoya J
Rev Neurol; 2003 Dec 1-15; 37(11):1029-31. PubMed ID: 14669142
[TBL] [Abstract][Full Text] [Related]
16. Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of mitochondrial DNA deletion in chronic progressive external ophthalmoplegia (CPEO).
Kwon MJ; Ki CS; Kim JY; Lee ST; Kim JW; Kang SY
Ann Clin Lab Sci; 2011; 41(4):385-9. PubMed ID: 22166510
[TBL] [Abstract][Full Text] [Related]
17. Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?
Auré K; Ogier de Baulny H; Laforêt P; Jardel C; Eymard B; Lombès A
Brain; 2007 Jun; 130(Pt 6):1516-24. PubMed ID: 17439982
[TBL] [Abstract][Full Text] [Related]
18. A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNA with multiple deletions.
Komaki H; Fukazawa T; Houzen H; Yoshida K; Nonaka I; Goto Y
Ann Neurol; 2002 May; 51(5):645-8. PubMed ID: 12112115
[TBL] [Abstract][Full Text] [Related]
19. [Chronic progressive external ophthalmoplegia (CPEO); mitochondrial DNA deletion, brain MRI and electrophysiological studies].
Nakagawa M; Tokimura M; Kuriyama M; Higuchi I; Osame M
Rinsho Shinkeigaku; 1991 Sep; 31(9):981-6. PubMed ID: 1769162
[TBL] [Abstract][Full Text] [Related]
20. [Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].
Pineda M; Playán-Ariso A; Alcaine-Villarroya MJ; Vernet AM; Serra-Castanera A; Solano A; Vilaseca MA; Artuch R; López-Pérez M; Briones-Godino MP; Andreu A; Montoya J
Rev Neurol; 2004 Jun 1-15; 38(11):1023-7. PubMed ID: 15202078
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
