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Journal Abstract Search

267 related items for PubMed ID: 24961732

  • 1. Adult onset Leigh syndrome with mitochondrial DNA 8344 A>G mutation.
    Han JY, Sung JJ, Park HK, Yoon BN, Lee KW.
    J Clin Neurosci; 2014 Nov; 21(11):2009-11. PubMed ID: 24961732
    [Abstract] [Full Text] [Related]

  • 2. Optic neuropathy in Lhon and Leigh syndrome.
    Carelli V, Sadun AA.
    Ophthalmology; 2001 Jul; 108(7):1172-3. PubMed ID: 11425664
    [No Abstract] [Full Text] [Related]

  • 3. Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options.
    Gerards M, Sallevelt SC, Smeets HJ.
    Mol Genet Metab; 2016 Mar; 117(3):300-12. PubMed ID: 26725255
    [Abstract] [Full Text] [Related]

  • 4. Fatigable ptosis as an initial presentation of adult-onset Leigh syndrome.
    Oh EH, Chae SH, Cho JW, Baik SK, Choi SY, Choi KD, Choi JH.
    Neurology; 2017 Oct 17; 89(16):1754. PubMed ID: 29038134
    [No Abstract] [Full Text] [Related]

  • 5. Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.
    Monden Y, Mori M, Kuwajima M, Goto T, Yamagata T, Momoi MY.
    Brain Dev; 2013 Jun 17; 35(6):582-5. PubMed ID: 22981260
    [Abstract] [Full Text] [Related]

  • 6. Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation.
    Ronchi D, Bordoni A, Cosi A, Rizzuti M, Fassone E, Di Fonzo A, Servida M, Sciacco M, Collotta M, Ronzoni M, Lucchini V, Mattioli M, Moggio M, Bresolin N, Corti S, Comi GP.
    Biochem Biophys Res Commun; 2011 Aug 26; 412(2):245-8. PubMed ID: 21819970
    [Abstract] [Full Text] [Related]

  • 7. Adult Leigh syndrome with mitochondrial DNA mutation at 8993.
    Nagashima T, Mori M, Katayama K, Nunomura M, Nishihara H, Hiraga H, Tanaka S, Goto Y, Nagashima K.
    Acta Neuropathol; 1999 Apr 26; 97(4):416-22. PubMed ID: 10208283
    [Abstract] [Full Text] [Related]

  • 8. Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C.
    Dermaut B, Seneca S, Dom L, Smets K, Ceulemans L, Smet J, De Paepe B, Tousseyn S, Weckhuysen S, Gewillig M, Pals P, Parizel P, De Bleecker JL, Boon P, De Meirleir L, De Jonghe P, Van Coster R, Van Paesschen W, Santens P.
    J Neurol Neurosurg Psychiatry; 2010 Jan 26; 81(1):90-3. PubMed ID: 20019223
    [Abstract] [Full Text] [Related]

  • 9. 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 26; 25(6):782-5. PubMed ID: 20332385
    [Abstract] [Full Text] [Related]

  • 10. Unusual findings in Leigh syndrome caused by T8993C mutation.
    Yiş U, Seneca S, Dirik E, Kurul SH, Ozer E, Cakmakçi H, De Meirleir L.
    Eur J Paediatr Neurol; 2009 Nov 26; 13(6):550-2. PubMed ID: 19046652
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 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 26; 11(3):1956-62. PubMed ID: 25384404
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy.
    Sweeney MG, Hammans SR, Duchen LW, Cooper JM, Schapira AH, Kennedy CR, Jacobs JM, Youl BD, Morgan-Hughes JA, Harding AE.
    J Neurol Sci; 1994 Jan 26; 121(1):57-65. PubMed ID: 8133313
    [Abstract] [Full Text] [Related]

  • 14. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.
    Pang CY, Huang CC, Yen MY, Wang EK, Kao KP, Chen SS, Wei YH.
    J Formos Med Assoc; 1999 May 26; 98(5):326-34. PubMed ID: 10420700
    [Abstract] [Full Text] [Related]

  • 15. [Leigh syndrome caused by the mitochondrial DNA G14459A mutation in a Mexican family].
    Gutiérrez A, Saldaña-Martínez A, García-Ramírez R, Rayo-Mares D, Carreras M, López-Pérez MJ, Ruiz-Pesini E, Montoya J, Montiel-Sosa JF.
    Rev Neurol; 1999 May 26; 49(5):248-50. PubMed ID: 19714555
    [Abstract] [Full Text] [Related]

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  • 17. Mitochondrial DNA point mutation T9176C in Leigh syndrome.
    Wilson CJ, Wood NW, Leonard JV, Surtees R, Rahman S.
    J Child Neurol; 2000 Dec 26; 15(12):830-3. PubMed ID: 11198506
    [Abstract] [Full Text] [Related]

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  • 20. Adult-Onset Leigh Syndrome Due to an m.13513G>A Mutation.
    Hirosawa H, Nukui T, Noguchi K, Nakatsuji Y.
    Intern Med; 2022 May 15; 61(10):1627-1628. PubMed ID: 34670906
    [No Abstract] [Full Text] [Related]

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