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Journal Abstract Search

162 related items for PubMed ID: 33779865

  • 1. Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation.
    Yu X, Ji K, Lin Y, Xu X, Wang W, Li Y, Lu JQ, Zhao Y, Yan C.
    Neurol Sci; 2021 Dec; 42(12):5123-5130. PubMed ID: 33779865
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  • 8. Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.
    Wang K, Takahashi Y, Gao ZL, Wang GX, Chen XW, Goto J, Lou JN, Tsuji S.
    Neurogenetics; 2009 Oct; 10(4):337-45. PubMed ID: 19458970
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  • 9. Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions.
    La Morgia C, Caporali L, Gandini F, Olivieri A, Toni F, Nassetti S, Brunetto D, Stipa C, Scaduto C, Parmeggiani A, Tonon C, Lodi R, Torroni A, Carelli V.
    BMC Neurol; 2014 May 28; 14():116. PubMed ID: 24884847
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  • 10. A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation.
    Saracchi E, Difrancesco JC, Brighina L, Marzorati L, Curtò NA, Lamperti C, Carrara F, Zeviani M, Ferrarese C.
    Neurol Sci; 2013 Mar 28; 34(3):407-8. PubMed ID: 22426787
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  • 13. Understanding the nomenclature of mitochondrial DNA mutations through examples of two specific disease entities: Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes and Leber hereditary optic neuropathy.
    Heuer B, Seibert DC.
    J Am Assoc Nurse Pract; 2022 Feb 01; 34(2):217-219. PubMed ID: 35120083
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  • 14. Leber's hereditary optic neuropathy with dystonia in a Japanese family.
    Watanabe M, Mita S, Takita T, Goto Y, Uchino M, Imamura S.
    J Neurol Sci; 2006 Apr 15; 243(1-2):31-4. PubMed ID: 16380132
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  • 17. [Mitochondrial diseases].
    Radelfahr F, Klopstock T.
    Nervenarzt; 2019 Feb 15; 90(2):121-130. PubMed ID: 30643957
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  • 19. Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
    De Vries DD, Went LN, Bruyn GW, Scholte HR, Hofstra RM, Bolhuis PA, van Oost BA.
    Am J Hum Genet; 1996 Apr 15; 58(4):703-11. PubMed ID: 8644732
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  • 20. Genetic counseling in Leber hereditary optic neuropathy (LHON).
    Huoponen K, Puomila A, Savontaus ML, Mustonen E, Kronqvist E, Nikoskelainen E.
    Acta Ophthalmol Scand; 2002 Feb 15; 80(1):38-43. PubMed ID: 11906302
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