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Journal Abstract Search

133 related items for PubMed ID: 12013911

  • 21. 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
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  • 22. 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
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  • 23. Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
    Zanssen S, Molnar M, Buse G, Schröder JM.
    Clin Neuropathol; 1998 Mar; 17(6):291-6. PubMed ID: 9832255
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  • 28. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S.
    N Engl J Med; 1989 May 18; 320(20):1293-9. PubMed ID: 2541333
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  • 30. A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea.
    De Block CE, De Leeuw IH, Maassen JA, Ballaux D, Martin JJ.
    Exp Clin Endocrinol Diabetes; 2004 Feb 18; 112(2):80-3. PubMed ID: 15031771
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  • 31. [Pigmented retinopathy as a presenting sign of mitochondrial encephalomyopathy without external ophthalmoplegia].
    Staudt S, Joussen AM, Rating D, Wilichowski E, Kolling G, Holz FG.
    Ophthalmologe; 2003 Mar 18; 100(3):234-7. PubMed ID: 12640554
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  • 32. Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA.
    Zoccolella S, Torraco A, Amati A, Lamberti P, Serlenga L, Papa S, Petruzzella V.
    Funct Neurol; 2006 Mar 18; 21(1):39-41. PubMed ID: 16735000
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  • 33. 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 22; 64(6):976-81. PubMed ID: 15781811
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  • 34. 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 22; 51(5):645-8. PubMed ID: 12112115
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  • 37. Pregnancy in chronic progressive external ophthalmoplegia: a case report.
    Ewart RM, Burrows RF.
    Am J Perinatol; 1997 May 22; 14(5):293-5. PubMed ID: 9259947
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  • 40. Sensorineural hearing loss in patients with chronic progressive external ophthalmoplegia or Kearns-Sayre syndrome.
    Kornblum C, Broicher R, Walther E, Herberhold S, Klockgether T, Herberhold C, Schröder R.
    J Neurol; 2005 Sep 22; 252(9):1101-7. PubMed ID: 15827867
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