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Journal Abstract Search

181 related items for PubMed ID: 8095070

  • 21. High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.
    Tsao CY, Mendell JR, Bartholomew D.
    J Child Neurol; 2001 Jul; 16(7):533-5. PubMed ID: 11453454
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  • 22. 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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  • 23. Dichloroacetate therapy in Leigh syndrome with a mitochondrial T8993C mutation.
    Fujii T, Ito M, Miyajima T, Okuno T.
    Pediatr Neurol; 2002 Jul; 27(1):58-61. PubMed ID: 12160976
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  • 24. [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; 2002 Jul; 34(12):1124-6. PubMed ID: 12134275
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  • 29. Phenotypic differences between T-->C and T-->G mutations at nt 8993 of mitochondrial DNA in Leigh syndrome.
    Fujii T, Hattori H, Higuchi Y, Tsuji M, Mitsuyoshi I.
    Pediatr Neurol; 1998 Mar; 18(3):275-7. PubMed ID: 9568930
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  • 31. Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene.
    Leshinsky-Silver E, Lev D, Tzofi-Berman Z, Cohen S, Saada A, Yanoov-Sharav M, Gilad E, Lerman-Sagie T.
    Biochem Biophys Res Commun; 2005 Aug 26; 334(2):582-7. PubMed ID: 16023078
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  • 35. A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.
    Chalmers RM, Lamont PJ, Nelson I, Ellison DW, Thomas NH, Harding AE, Hammans SR.
    Neurology; 1997 Aug 26; 49(2):589-92. PubMed ID: 9270602
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  • 36. De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring.
    Tulinius MH, Houshmand M, Larsson NG, Holme E, Oldfors A, Holmberg E, Wahlström J.
    Hum Genet; 1995 Sep 26; 96(3):290-4. PubMed ID: 7649544
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