These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
293 related articles for article (PubMed ID: 8513327)
1. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies. Brockington M; Sweeney MG; Hammans SR; Morgan-Hughes JA; Harding AE Nat Genet; 1993 May; 4(1):67-71. PubMed ID: 8513327 [TBL] [Abstract][Full Text] [Related]
2. Ocular myopathy and mitochondrial DNA deletion. A presentation of seven identified Danish patients. Magalhães PJ; Sjö O; Nørby S Acta Ophthalmol Scand Suppl; 1996; (219):29-32. PubMed ID: 8741113 [TBL] [Abstract][Full Text] [Related]
3. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies. Filosto M; Mancuso M; Vives-Bauza C; Vilà MR; Shanske S; Hirano M; Andreu AL; DiMauro S Ann Neurol; 2003 Oct; 54(4):524-6. PubMed ID: 14520667 [TBL] [Abstract][Full Text] [Related]
4. [Deletions of mitochondrial DNA in Kearns-Sayre syndrome]. Soga F; Ueno S; Yorifuji S Nihon Rinsho; 1993 Sep; 51(9):2386-90. PubMed ID: 8411717 [TBL] [Abstract][Full Text] [Related]
5. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy. Ohno K; Yamamoto M; Engel AG; Harper CM; Roberts LR; Tan GH; Fatourechi V Ann Neurol; 1996 Jun; 39(6):761-6. PubMed ID: 8651648 [TBL] [Abstract][Full Text] [Related]
6. Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid. Tengan CH; Kiyomoto BH; Rocha MS; Tavares VL; Gabbai AA; Moraes CT J Clin Endocrinol Metab; 1998 Jan; 83(1):125-9. PubMed ID: 9435428 [TBL] [Abstract][Full Text] [Related]
7. 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]
9. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy]. Ito T Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824 [TBL] [Abstract][Full Text] [Related]
10. [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]
11. Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome. Ota Y; Tanaka M; Sato W; Ohno K; Yamamoto T; Maehara M; Negoro T; Watanabe K; Awaya S; Ozawa T Invest Ophthalmol Vis Sci; 1991 Sep; 32(10):2667-75. PubMed ID: 1894466 [TBL] [Abstract][Full Text] [Related]
12. Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence. Remes AM; Peuhkurinen KJ; Herva R; Majamaa K; Hassinen IE Genomics; 1993 Apr; 16(1):256-8. PubMed ID: 7683627 [TBL] [Abstract][Full Text] [Related]
13. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome]. Capková M; Tesarová M; Wenchich L; Cerná L; Hansíková H; Hůlková H; Hrubá E; Elleder M; Zeman J Cas Lek Cesk; 2002 Feb; 141(2):51-4. PubMed ID: 11925663 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation. Barthélémy C; Ogier de Baulny H; Diaz J; Cheval MA; Frachon P; Romero N; Goutieres F; Fardeau M; Lombès A Ann Neurol; 2001 May; 49(5):607-17. PubMed ID: 11357951 [TBL] [Abstract][Full Text] [Related]
16. POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions. Di Fonzo A; Bordoni A; Crimi M; Sara G; Del Bo R; Bresolin N; Comi GP Hum Mutat; 2003 Dec; 22(6):498-9. PubMed ID: 14635118 [TBL] [Abstract][Full Text] [Related]
17. [Multiple mitochondrial DNA deletions in cardiomyopathy]. Hattori K Nihon Rinsho; 1993 Jun; 51(6):1429-34. PubMed ID: 8320825 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. 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] [Next] [New Search]