245 related articles for article (PubMed ID: 14669142)
1. [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]
2. [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]
3. 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; 40(5):707-13. PubMed ID: 8957011
[TBL] [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; 105(5):180-4. PubMed ID: 7630231
[TBL] [Abstract][Full Text] [Related]
5. Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3,399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA.
Thajeb P; Ma YS; Tzen CY; Chuang CK; Wu TY; Chen SC; Wei YH
Clin Neurol Neurosurg; 2006 Jun; 108(4):407-10. PubMed ID: 16644408
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. The common deletion found in patient reexamined after 33 years and comparison with complete mtDNA sequences of maternal relatives.
Levin BC; Sekiguchi K; Tully LA; Chen TL; Gropman A
Mitochondrion; 2005 Dec; 5(6):403-10. PubMed ID: 16172025
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. [Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].
Laforêt P; Eymard B; Danan C; Chevallay M; Rouche A; Frachon P; Fardeau M; Lombès A
Rev Neurol (Paris); 1997 Feb; 153(1):51-8. PubMed ID: 9296156
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis.
Taylor RW; Chinnery PF; Bates MJ; Jackson MJ; Johnson MA; Andrews RM; Turnbull DM
Biochem Biophys Res Commun; 1998 Feb; 243(1):47-51. PubMed ID: 9473477
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant chronic progressive external ophthalmoplegia: a tale of two genomes.
Shoubridge EA
Ann Neurol; 1996 Nov; 40(5):693-4. PubMed ID: 8957008
[No Abstract] [Full Text] [Related]
19. CPEO and KSS differ in the percentage and location of the mtDNA deletion.
López-Gallardo E; López-Pérez MJ; Montoya J; Ruiz-Pesini E
Mitochondrion; 2009 Sep; 9(5):314-7. PubMed ID: 19410662
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
