221 related articles for article (PubMed ID: 11245066)
21. Progressive external ophthalmoplegia and multiple mitochondrial DNA deletions.
Van Goethem G; Martin JJ; Van Broeckhoven C
Acta Neurol Belg; 2002 Mar; 102(1):39-42. PubMed ID: 12094562
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) gene.
Seibel P; Lauber J; Klopstock T; Marsac C; Kadenbach B; Reichmann H
Biochem Biophys Res Commun; 1994 Oct; 204(2):482-9. PubMed ID: 7980504
[TBL] [Abstract][Full Text] [Related]
24. False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites.
Weglewska-Jurkiewicz A; Jakóbkiewicz-Banecka J; Pronicka E; Wegrzyn G
Diagn Mol Pathol; 2007 Jun; 16(2):116-20. PubMed ID: 17525683
[TBL] [Abstract][Full Text] [Related]
25. [A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA].
Hoshino S; Tamaoka A; Ohkoshi N; Shoji S; Goto Y
Rinsho Shinkeigaku; 1997 Apr; 37(4):326-30. PubMed ID: 9248343
[TBL] [Abstract][Full Text] [Related]
26. A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.
Tabaku M; Legius E; Robberecht W; Sciot R; Fryns JP; Cassiman JJ; Matthijs G
Genet Couns; 1999; 10(3):285-93. PubMed ID: 10546101
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. [Mutation analysis of mitochondrial DNA of children with Rett syndrome].
Tang J; Qi Y; Bao X
Zhonghua Yi Xue Za Zhi; 1996 Sep; 76(9):684-7. PubMed ID: 9275552
[TBL] [Abstract][Full Text] [Related]
30. Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population.
Remes AM; Majamaa-Voltti K; Kärppä M; Moilanen JS; Uimonen S; Helander H; Rusanen H; Salmela PI; Sorri M; Hassinen IE; Majamaa K
Neurology; 2005 Mar; 64(6):976-81. PubMed ID: 15781811
[TBL] [Abstract][Full Text] [Related]
31. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.
Van Goethem G; Dermaut B; Löfgren A; Martin JJ; Van Broeckhoven C
Nat Genet; 2001 Jul; 28(3):211-2. PubMed ID: 11431686
[TBL] [Abstract][Full Text] [Related]
32. A novel mitochondrial DNA deletion producing progressive external ophthalmoplegia associated with multiple sclerosis.
Slee M; Finkemeyer J; Krupa M; Raghupathi R; Gardner J; Blumbergs P; Agzarian M; Thyagarajan D
J Clin Neurosci; 2011 Oct; 18(10):1318-24. PubMed ID: 21795050
[TBL] [Abstract][Full Text] [Related]
33. [Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA].
Tanno Y; Yoneda M; Ohnishi Y; Miyatake T; Ozawa T
Rinsho Shinkeigaku; 1989 Sep; 29(9):1176-9. PubMed ID: 2598547
[TBL] [Abstract][Full Text] [Related]
34. [A case of chronic progressive external ophthalmoplegia associated with familial hypercholesterolemia].
Orimo S; Arai M; Hiyamuta E; Goto Y
Rinsho Shinkeigaku; 1992 Jan; 32(1):37-41. PubMed ID: 1628435
[TBL] [Abstract][Full Text] [Related]
35. [A mitochondrial DNA mutation in the heteroplasmic tRNA-Tyr gene associated with chronic progressive external ophthalmoplegia--clinical and molecular biological study].
Sahashi K; Ibi T; Yoneda M; Tanaka M; Ohno K
Nihon Rinsho; 1997 Dec; 55(12):3265-9. PubMed ID: 9436448
[TBL] [Abstract][Full Text] [Related]
36. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
[TBL] [Abstract][Full Text] [Related]
37. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
[TBL] [Abstract][Full Text] [Related]
38. Deletion screening of mitochondrial DNA via multiprimer DNA amplification.
Ernst BP; Wilichowski E; Wagner M; Hanefeld F
Mol Cell Probes; 1994 Feb; 8(1):45-9. PubMed ID: 8028607
[TBL] [Abstract][Full Text] [Related]
39. Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype.
Jackson CB; Neuwirth C; Hahn D; Nuoffer JM; Frank S; Gallati S; Schaller A
Br J Ophthalmol; 2014 Oct; 98(10):1453-9. PubMed ID: 25034047
[TBL] [Abstract][Full Text] [Related]
40. Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia.
Houshmand M; Panahi MS; Hosseini BN; Dorraj GH; Tabassi AR
Neurol India; 2006 Jun; 54(2):182-5. PubMed ID: 16804265
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]