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PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 11182283

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  • 2. 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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  • 4. Mitochondrial DNA depletion in Leigh syndrome.
    Filiano JJ, Goldenthal MJ, Mamourian AC, Hall CC, Marín-García J.
    Pediatr Neurol; 2002 Mar; 26(3):239-42. PubMed ID: 11955936
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  • 5. 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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  • 8. 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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  • 12. Mild clinical manifestation and unusual recovery upon coenzyme Q₁₀ treatment in the first Chinese Leigh syndrome pedigree with mutation m.10197 G>A.
    Chen Z, Zhao Z, Ye Q, Chen Y, Pan X, Sun B, Huang H, Zheng A.
    Mol Med Rep; 2015 Mar; 11(3):1956-62. PubMed ID: 25384404
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  • 15. Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.
    García-Silva MT, Ribes A, Campos Y, Garavaglia B, Arenas J.
    Pediatr Neurol; 1997 Sep; 17(2):165-70. PubMed ID: 9367300
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  • 20. Maternally inherited Leigh syndrome: an unusual cause of infantile apnea.
    Shuk-kuen Chau C, Kwok KL, Ng DK, Lam CW, Tong SF, Chan YW, Siu WK, Yuen YP.
    Sleep Breath; 2010 Jun; 14(2):161-5. PubMed ID: 19669818
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