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PUBMED FOR HANDHELDS

Journal Abstract Search

264 related items for PubMed ID: 10894222

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  • 42. Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA.
    White SL, Shanske S, Biros I, Warwick L, Dahl HM, Thorburn DR, Di Mauro S.
    Prenat Diagn; 1999 Dec; 19(12):1165-8. PubMed ID: 10590437
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  • 50. Mitochondrial DNA point mutation T9176C in Leigh syndrome.
    Wilson CJ, Wood NW, Leonard JV, Surtees R, Rahman S.
    J Child Neurol; 2000 Dec; 15(12):830-3. PubMed ID: 11198506
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  • 51. Complex I function in familial and sporadic dystonia.
    Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM.
    Ann Neurol; 1997 Apr; 41(4):556-9. PubMed ID: 9124815
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  • 52. Mutation of mitochondrial DNA G13513A presenting with Leigh syndrome, Wolff-Parkinson-White syndrome and cardiomyopathy.
    Wang SB, Weng WC, Lee NC, Hwu WL, Fan PC, Lee WT.
    Pediatr Neonatol; 2008 Aug; 49(4):145-9. PubMed ID: 19054921
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  • 53. Leigh syndrome presenting with dystonia: report of one case.
    Huang WY, Chi CS, Mak SC, Wu HM, Yang MT.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1995 Aug; 36(5):378-81. PubMed ID: 8607367
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  • 56. Cardiac mitochondrial dysfunction in Leigh syndrome.
    Marin-Garcia J, Ananthakrishnan R, Korson M, Goldenthal MJ, Perez-Atayde A.
    Pediatr Cardiol; 1996 Aug; 17(6):387-9. PubMed ID: 8781089
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  • 57. Optic neuropathy in Lhon and Leigh syndrome.
    Carelli V, Sadun AA.
    Ophthalmology; 2001 Jul; 108(7):1172-3. PubMed ID: 11425664
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  • 58. Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C.
    Tarnopolsky M, Meaney B, Robinson B, Sheldon K, Boles RG.
    Am J Med Genet A; 2013 Aug; 161A(8):2020-3. PubMed ID: 23813926
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  • 59. Maternally inherited Leigh syndrome.
    Ciafaloni E, Santorelli FM, Shanske S, Deonna T, Roulet E, Janzer C, Pescia G, DiMauro S.
    J Pediatr; 1993 Mar; 122(3):419-22. PubMed ID: 8095070
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