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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. Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis. Okulla T; Kunz WS; Klockgether T; Schröder R; Kornblum C Graefes Arch Clin Exp Ophthalmol; 2005 Apr; 243(4):380-2. PubMed ID: 15864628 [TBL] [Abstract][Full Text] [Related]
14. [A case of chronic progressive external ophthalmoplegia presenting as inflammatory myopathy]. Fujimoto S; Ueyama H; Mita S; Kumamoto T; Tsuda T Rinsho Shinkeigaku; 1998 Mar; 38(3):228-32. PubMed ID: 9711119 [TBL] [Abstract][Full Text] [Related]
15. Ptosis as an associated finding in maternally inherited diabetes and deafness. Robberecht K; Decock C; Stevens A; Seneca S; De Bleecker J; Leroy BP Ophthalmic Genet; 2010 Dec; 31(4):240-3. PubMed ID: 21067488 [TBL] [Abstract][Full Text] [Related]
16. [Progressive external ophthalmoplegia with extensive mitochondrial DNA deletion]. Munakata S; Yamazaki H; Sato T Nippon Ganka Gakkai Zasshi; 1994 Oct; 98(10):1036-42. PubMed ID: 7976825 [TBL] [Abstract][Full Text] [Related]
17. 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]
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19. [Chronic progressive external ophthalmoplegia: clinical and electromyographic manifestations in a series of cases]. Jiménez-Caballero PE; Serviá M; Cabeza CI; Marsal-Alonso C; Alvarez-Tejerina A Rev Neurol; 2006 Dec 16-31; 43(12):724-8. PubMed ID: 17160922 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]