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Journal Abstract Search

182 related items for PubMed ID: 15493224

  • 21. Heart diseases in mitochondrial encephalomyopathy, lactic acidosis, and stroke syndrome.
    Fayssoil A.
    Congest Heart Fail; 2009; 15(6):284-7. PubMed ID: 19925507
    [Abstract] [Full Text] [Related]

  • 22. Clinical features of MELAS and its relation with A3243G gene point mutation.
    Zhang J, Guo J, Fang W, Jun Q, Shi K.
    Int J Clin Exp Pathol; 2015; 8(10):13411-5. PubMed ID: 26722549
    [Abstract] [Full Text] [Related]

  • 23. Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree.
    Dubeau F, De Stefano N, Zifkin BG, Arnold DL, Shoubridge EA.
    Ann Neurol; 2000 Feb; 47(2):179-85. PubMed ID: 10665488
    [Abstract] [Full Text] [Related]

  • 24. Nerve conduction abnormalities in patients with MELAS and the A3243G mutation.
    Kaufmann P, Pascual JM, Anziska Y, Gooch CL, Engelstad K, Jhung S, DiMauro S, De Vivo DC.
    Arch Neurol; 2006 May; 63(5):746-8. PubMed ID: 16682545
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. [Unexceptional symptoms as expression of MELAS].
    van Rossum IA, ten Houten R.
    Ned Tijdschr Geneeskd; 2010 Sep; 154():A2168. PubMed ID: 21083956
    [Abstract] [Full Text] [Related]

  • 27. An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
    Ravn K, Wibrand F, Hansen FJ, Horn N, Rosenberg T, Schwartz M.
    Eur J Hum Genet; 2001 Oct; 9(10):805-9. PubMed ID: 11781695
    [Abstract] [Full Text] [Related]

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

  • 29. Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g).
    Tzen CY, Thajeb P, Wu TY, Chen SC.
    Muscle Nerve; 2003 Nov; 28(5):575-81. PubMed ID: 14571459
    [Abstract] [Full Text] [Related]

  • 30. [Infantile encephalopathy associated with the MELAS A3243G mutation. Case report].
    Guevara-Campos J, Gonzalez-Guevara L, Parada Y, Urbáez-Cano J.
    Invest Clin; 2007 Jun; 48(2):243-8. PubMed ID: 17598646
    [Abstract] [Full Text] [Related]

  • 31. 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]

  • 32. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
    Horváth R, Reilmann R, Holinski-Feder E, Ringelstein EB, Klopstock T.
    Neuromuscul Disord; 2008 Jul 15; 18(7):553-6. PubMed ID: 18590963
    [Abstract] [Full Text] [Related]

  • 33. Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA.
    Tay SK, Shanske S, Crowe C, Shanske A, Schafer I, Pancrudo J, Lu J, Bonilla E, DiMauro S.
    J Child Neurol; 2005 Feb 15; 20(2):142-6. PubMed ID: 15794182
    [Abstract] [Full Text] [Related]

  • 34. [A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA].
    Hoshino S, Tamaoka A, Ohkoshi N, Shoji S, Goto Y.
    Rinsho Shinkeigaku; 1997 Apr 15; 37(4):326-30. PubMed ID: 9248343
    [Abstract] [Full Text] [Related]

  • 35. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Donegal kindred--clinical features and molecular genetic analysis.
    McEntagart M, Droogan O, Burke M, Brett F, Murphy S, Farrell M.
    Ir Med J; 1997 Apr 15; 90(4):144-5. PubMed ID: 9267093
    [Abstract] [Full Text] [Related]

  • 36. [Analysis of clinical phenotype in 42 nuclear pedigrees carrying mitochondrial DNA A3243G mutation].
    Ma YN, Fang F, Cao YY, Yang YL, Zou LP, Zhang Y, Wang ST, Zhu SN, Li L, Zheng XF, Pei P, Wu HR, Xiao Y, Qi Y.
    Zhonghua Yi Xue Za Zhi; 2010 Dec 07; 90(45):3184-7. PubMed ID: 21223764
    [Abstract] [Full Text] [Related]

  • 37. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.
    Li JY, Hsieh RH, Peng NJ, Lai PH, Lee CF, Lo YK, Wei YH.
    J Formos Med Assoc; 2007 Jul 07; 106(7):528-36. PubMed ID: 17660142
    [Abstract] [Full Text] [Related]

  • 38. Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation.
    Komlósi K, Kellermayer R, Maász A, Havasi V, Hollódy K, Vincze O, Merkli H, Pál E, Melegh B.
    Pathol Oncol Res; 2005 Jul 07; 11(2):82-6. PubMed ID: 15999151
    [Abstract] [Full Text] [Related]

  • 39. Mitochondrial genetic analysis in a Chinese family suffering from both mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes and diabetes.
    Li W, Zhang W, Li F, Wang C.
    Int J Clin Exp Pathol; 2015 Jul 07; 8(6):7022-7. PubMed ID: 26261593
    [Abstract] [Full Text] [Related]

  • 40. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
    Spruijt L, Smeets HJ, Hendrickx A, Bettink-Remeijer MW, Maat-Kievit A, Schoonderwoerd KC, Sluiter W, de Coo IF, Hintzen RQ.
    Arch Neurol; 2007 Jun 07; 64(6):890-3. PubMed ID: 17562939
    [Abstract] [Full Text] [Related]

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