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Journal Abstract Search

442 related items for PubMed ID: 11562875

  • 1. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M, Díaz-Guzmán J, Pérez-Martínez DA, Sáiz-Díaz RA, Rodríguez-Vallejo A, Campos Y.
    Rev Neurol; ; 33(2):148-50. PubMed ID: 11562875
    [Abstract] [Full Text] [Related]

  • 2. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
    [Abstract] [Full Text] [Related]

  • 3. Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Chen JC, Tsai TC, Liu CS, Lu CT.
    Acta Neurol Taiwan; 2007 Sep; 16(3):168-72. PubMed ID: 17966957
    [Abstract] [Full Text] [Related]

  • 4. Adult-onset of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presenting as acute meningoencephalitis: a case report.
    Hsu YC, Yang FC, Perng CL, Tso AC, Wong LJ, Hsu CH.
    J Emerg Med; 2012 Sep; 43(3):e163-6. PubMed ID: 20036095
    [Abstract] [Full Text] [Related]

  • 5. [Unexceptional symptoms as expression of MELAS].
    van Rossum IA, ten Houten R.
    Ned Tijdschr Geneeskd; 2010 Sep; 154():A2168. PubMed ID: 21083956
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  • 8. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov; 110(11):851-5. PubMed ID: 9772417
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  • 9. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
    [Abstract] [Full Text] [Related]

  • 10. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796
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  • 11. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
    [Abstract] [Full Text] [Related]

  • 12. MELAS masquerading as a systemic vasculitis.
    Carroll MB.
    J Clin Rheumatol; 2007 Dec 15; 13(6):334-7. PubMed ID: 18176143
    [Abstract] [Full Text] [Related]

  • 13. Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Santa KM.
    Pharmacotherapy; 2010 Nov 15; 30(11):1179-96. PubMed ID: 20973690
    [Abstract] [Full Text] [Related]

  • 14. Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELAS.
    Takahashi K, Merchant SN, Miyazawa T, Yamaguchi T, McKenna MJ, Kouda H, Iino Y, Someya T, Tamagawa Y, Takiyama Y, Nakano I, Saito K, Boyer P, Kitamura K.
    Laryngoscope; 2003 Aug 15; 113(8):1362-8. PubMed ID: 12897560
    [Abstract] [Full Text] [Related]

  • 15. Diversity of clinical symptoms in A3243G mitochondrial DNA mutation (MELAS syndrome mutation).
    Pronicki M, Sykut-Cegielska J, Mierzewska H, Tońska K, Karczmarewicz E, Iwanicka K, Bartnik E, Pronicka E.
    Med Sci Monit; 2002 Nov 15; 8(11):CR767-73. PubMed ID: 12444382
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  • 17. [MELAS presenting herpes simplex encephalitis].
    Ogata A, Mitsumori K.
    Nihon Rinsho; 2002 Apr 15; 60 Suppl 4():629-31. PubMed ID: 12013959
    [No Abstract] [Full Text] [Related]

  • 18. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome mimicking herpes simplex encephalitis on imaging studies.
    Gieraerts C, Demaerel P, Van Damme P, Wilms G.
    J Comput Assist Tomogr; 2013 Apr 15; 37(2):279-81. PubMed ID: 23493219
    [Abstract] [Full Text] [Related]

  • 19. [Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].
    Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B.
    Orv Hetil; 2004 Aug 29; 145(35):1805-9. PubMed ID: 15493224
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  • 20. MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation.
    Connolly BS, Feigenbaum AS, Robinson BH, Dipchand AI, Simon DK, Tarnopolsky MA.
    Biochem Biophys Res Commun; 2010 Nov 12; 402(2):443-7. PubMed ID: 20965148
    [Abstract] [Full Text] [Related]

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