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243 related items for PubMed ID: 11510939

  • 1. Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome.
    Cacić M, Wilichowski E, Mejaski-Bosnjak V, Fumić K, Lujić L, Marusić Della Marina B, Hanefeld F.
    J Child Neurol; 2001 Aug; 16(8):616-9. PubMed ID: 11510939
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  • 2. Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.
    Savasta S, Comi GP, Perini MP, Lupi A, Strazzer S, Rognoni F, Rossoni R.
    J Child Neurol; 2001 Aug; 16(8):608-13. PubMed ID: 11510937
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  • 3. Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome.
    Zafeiriou DI, Koletzko B, Mueller-Felber W, Paetzke I, Kueffer G, Jensen M.
    Brain Dev; 1995 Aug; 17(2):117-21. PubMed ID: 7625545
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  • 4. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
    Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR.
    Chin Med J (Engl); 2006 Mar 05; 119(5):373-7. PubMed ID: 16542579
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  • 5. [Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases].
    Castro-Gago M, González-Conde V, Fernández-Seara MJ, Rodrigo-Sáez E, Fernández-Cebrián S, Alonso-Martín A, Campos Y, Arenas J, Eirís-Puñal J.
    Rev Neurol; 2006 Mar 05; 29(10):912-7. PubMed ID: 10637838
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  • 9. Leigh syndrome in an infant resulting from mitochondrial DNA depletion.
    Absalon MJ, Harding CO, Fain DR, Li L, Mack KJ.
    Pediatr Neurol; 2001 Jan 05; 24(1):60-3. PubMed ID: 11182283
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  • 14. [A mitochondrial encephalomyopathy due to partial cytochrome c oxidase deficiency with giant evoked potentials--a case report].
    Higashi Y, Higashi S, Terao A, Yasuda T, Shirabe T.
    Rinsho Shinkeigaku; 1990 Oct 05; 30(10):1084-9. PubMed ID: 2177689
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  • 15. A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.
    Bruno C, Biancheri R, Garavaglia B, Biedi C, Rossi A, Lamba LD, Bado M, Greco M, Zeviani M, Minetti C.
    J Child Neurol; 2002 Mar 05; 17(3):233-6. PubMed ID: 12026244
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  • 16. Diagnosis and treatment in a case of juvenile subacute necrotizing encephalopathy Leigh without cytochrome c oxidase deficiency.
    Westarp ME, Holzgraefe M, Gallenkamp U, Thomas R, Bechinger D.
    Eur Neurol; 1992 Mar 05; 32(4):206-11. PubMed ID: 1324178
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