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127 related items for PubMed ID: 21427669

  • 1. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.
    Lu J, He B, Wang D.
    Neurosciences (Riyadh); 2011 Apr; 16(2):162-3. PubMed ID: 21427669
    [No Abstract] [Full Text] [Related]

  • 2. Marked left ventricular hypertrophy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
    Takahashi N, Shimada T, Ishibashi Y, Yoshitomi H, Oyake N, Murakami Y, Nishino I, Nonaka I, Goto Y, Kitamura J.
    Int J Cardiol; 2008 Oct 13; 129(3):e77-80. PubMed ID: 17900719
    [No Abstract] [Full Text] [Related]

  • 3. Mitochondrial encephalomyopathy lactic acidosis and strokelike episodes mimicking occipital idiopathic epilepsy.
    Cesaroni E, Scarpelli M, Zamponi N, Polonara G, Zeviani M.
    Pediatr Neurol; 2009 Aug 13; 41(2):131-4. PubMed ID: 19589463
    [Abstract] [Full Text] [Related]

  • 4. [Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].
    Suzuki S.
    Nihon Rinsho; 1994 Oct 13; 52(10):2606-10. PubMed ID: 7527090
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes in a 69-year-old woman.
    Molaee P, Dundon BK.
    Intern Med J; 2008 Jun 13; 38(6):451-2. PubMed ID: 18613903
    [No Abstract] [Full Text] [Related]

  • 6. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA.
    Terauchi A, Tamagawa K, Morimatsu Y, Kobayashi M, Sano T, Yoda S.
    Brain Dev; 1996 Jun 13; 18(3):224-9. PubMed ID: 8836506
    [Abstract] [Full Text] [Related]

  • 7. Acute blindness.
    Abboud H, Sabbagh C.
    Emerg Med J; 2008 Nov 13; 25(11):779-80. PubMed ID: 18955627
    [Abstract] [Full Text] [Related]

  • 8. Teaching NeuroImages: mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes.
    Allou T, Castelnovo G, Renard D.
    Neurology; 2012 Oct 02; 79(14):e125. PubMed ID: 23033508
    [No Abstract] [Full Text] [Related]

  • 9. A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome.
    Emmanuele V, Sotiriou E, Rios PG, Ganesh J, Ichord R, Foley AR, Akman HO, Dimauro S.
    J Child Neurol; 2013 Feb 02; 28(2):236-42. PubMed ID: 22638077
    [Abstract] [Full Text] [Related]

  • 10. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
    Song D, Zhang Y, Shi J, Lü Q, Chen J, Zhang H, Zhang W, Wang H, Cai Q.
    Chin Med J (Engl); 2001 Dec 02; 114(12):1273-5. PubMed ID: 11793851
    [Abstract] [Full Text] [Related]

  • 11. Fundus changes in patients with the mitochondrial DNA point mutation at position 3243.
    Bonte C, Leys A, Matthijs G, Missotten L.
    Bull Soc Belge Ophtalmol; 1996 Dec 02; 261():9-12. PubMed ID: 9009357
    [Abstract] [Full Text] [Related]

  • 12. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure.
    Yanagihara C, Oyama A, Tanaka M, Nakaji K, Nishimura Y.
    Intern Med; 2001 Jul 02; 40(7):662-5. PubMed ID: 11506313
    [Abstract] [Full Text] [Related]

  • 13. Choroidal Pigmentary Streaks in Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-like Episodes Syndrome.
    Ramtohul P, Chehaibou I, Bonnin S.
    Ophthalmol Retina; 2021 May 02; 5(5):486. PubMed ID: 33962759
    [No Abstract] [Full Text] [Related]

  • 14. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.
    Sproule DM, Kaufmann P.
    Ann N Y Acad Sci; 2008 Oct 02; 1142():133-58. PubMed ID: 18990125
    [Abstract] [Full Text] [Related]

  • 15. Pitfalls in the diagnosis of mitochondrial encephalopathy with lactic acidosis and stroke-like episodes.
    Mizrachi IB, Gomez-Hassan D, Blaivas M, Trobe JD.
    J Neuroophthalmol; 2006 Mar 02; 26(1):38-43. PubMed ID: 16518165
    [Abstract] [Full Text] [Related]

  • 16. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb 02; 27(1):77-80. PubMed ID: 15782498
    [Abstract] [Full Text] [Related]

  • 17. A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.
    Campos Y, Lorenzo G, Martín MA, Torregrosa A, del Hoyo P, Rubio JC, García A, Arenas J.
    Neuromuscul Disord; 2000 Oct 02; 10(7):493-6. PubMed ID: 10996780
    [Abstract] [Full Text] [Related]

  • 18. SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.
    Carrozzo R, Dionisi-Vici C, Steuerwald U, Lucioli S, Deodato F, Di Giandomenico S, Bertini E, Franke B, Kluijtmans LA, Meschini MC, Rizzo C, Piemonte F, Rodenburg R, Santer R, Santorelli FM, van Rooij A, Vermunt-de Koning D, Morava E, Wevers RA.
    Brain; 2007 Mar 02; 130(Pt 3):862-74. PubMed ID: 17301081
    [Abstract] [Full Text] [Related]

  • 19. Sigmoid volvulus in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): a rare occurrence.
    Hallac A, Keshava HB, Morris-Stiff G, Ibrahim S.
    BMJ Case Rep; 2016 Mar 02; 2016():. PubMed ID: 26935953
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report.
    Gunawardena K, Praveenan S, Dissanayake VHW, Ratnayake P.
    J Med Case Rep; 2024 Sep 04; 18(1):420. PubMed ID: 39252049
    [Abstract] [Full Text] [Related]

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