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Journal Abstract Search

355 related items for PubMed ID: 19144360

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  • 2. [Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)].
    Playán A, Solano-Palacios A, González de la Rosa JB, Merino-Arribas JM, Andreu AL, López-Pérez M, Montoya J.
    Rev Neurol; ; 34(12):1124-6. PubMed ID: 12134275
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  • 5. Novel mitochondrial mutation in the ND4 gene associated with Leigh syndrome.
    Vanniarajan A, Rajshekher GP, Joshi MB, Reddy AG, Singh L, Thangaraj K.
    Acta Neurol Scand; 2006 Nov; 114(5):350-3. PubMed ID: 17022785
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  • 11. Leigh syndrome: clinical and neuroimaging follow-up.
    Lee HF, Tsai CR, Chi CS, Lee HJ, Chen CC.
    Pediatr Neurol; 2009 Feb; 40(2):88-93. PubMed ID: 19135620
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  • 13. A previously undescribed leukodystrophy in Leigh syndrome associated with T9176C mutation of the mitochondrial ATPase 6 gene.
    Hung PC, Wang HS.
    Dev Med Child Neurol; 2007 Jan; 49(1):65-7. PubMed ID: 17209980
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  • 14. SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.
    Carrozzo R, Dionisi-Vici C, Steuerwald U, Lucioli S, Deodato F, Di Giandomenico S, Bertini E, Franke B, Kluijtmans LA, Meschini MC, Rizzo C, Piemonte F, Rodenburg R, Santer R, Santorelli FM, van Rooij A, Vermunt-de Koning D, Morava E, Wevers RA.
    Brain; 2007 Mar; 130(Pt 3):862-74. PubMed ID: 17301081
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  • 17. A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.
    de Vries DD, van Engelen BG, Gabreëls FJ, Ruitenbeek W, van Oost BA.
    Ann Neurol; 1993 Sep; 34(3):410-2. PubMed ID: 8395787
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  • 19. A novel presentation of inappropriate antidiuretic hormone secretion in Leigh syndrome with the myoclonic epilepsy and ragged red fibers, mitochondrial DNA 8344A>G mutation.
    Swiderska N, Appleton R, Morris A, Isherwood D, Selby A.
    J Child Neurol; 2010 Jun; 25(6):782-5. PubMed ID: 20332385
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  • 20. Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.
    Funalot B, Reynier P, Vighetto A, Ranoux D, Bonnefont JP, Godinot C, Malthièry Y, Mas JL.
    Ann Neurol; 2002 Sep; 52(3):374-7. PubMed ID: 12205655
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