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Journal Abstract Search

152 related items for PubMed ID: 22426787

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  • 5. Leber optic hereditary neuropathy plus dystonia.
    Mahoui S, Belkhamsa O, Ait Kaci I, Abada Bendib M, Castelnovo G.
    Rev Neurol (Paris); 2019; 175(7-8):483-484. PubMed ID: 31221418
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  • 6. Pediatric-onset dystonia associated with bilateral striatal necrosis and G14459A mutation in a Korean family: a case report.
    Kim IS, Ki CS, Park KJ.
    J Korean Med Sci; 2010 Jan; 25(1):180-4. PubMed ID: 20052369
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  • 9. Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation.
    Fruhman G, Landsverk ML, Lotze TE, Hunter JV, Wangler MF, Adesina AM, Wong LJ, Scaglia F.
    Mol Genet Metab; 2011 Jun; 103(2):153-60. PubMed ID: 21414825
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  • 15. Posterior reversible encephalopathy syndrome in a leber hereditary optic neuropathy patient with mitochondrial DNA 11778G>A point mutation.
    Da Y, Zhang X, Li F, Yang X, Zhang X, Jia J.
    J Neuroophthalmol; 2013 Sep; 33(3):276-8. PubMed ID: 23782927
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  • 16. Co-occurrence of amyotrophic lateral sclerosis and Leber's hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
    Amore G, Vacchiano V, La Morgia C, Valentino ML, Caporali L, Fiorini C, Ormanbekova D, Salvi F, Bartoletti-Stella A, Capellari S, Liguori R, Carelli V.
    J Neurol; 2023 Jan; 270(1):559-564. PubMed ID: 36066624
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  • 19. Painful vision loss in Leber hereditary optic neuropathy with novel ND1 variant mimicking optic neuritis.
    Alkabie S, Fraser JA, Racosta J.
    Can J Ophthalmol; 2023 Feb; 58(1):e40-e42. PubMed ID: 35809626
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  • 20. Demyelinating polyneuropathy in Leber hereditary optic neuropathy.
    Gilhuis HJ, Schelhaas HJ, Cruysberg JR, Zwarts MJ.
    Neuromuscul Disord; 2006 Jun; 16(6):394-5. PubMed ID: 16690316
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