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Journal Abstract Search

187 related items for PubMed ID: 16551460

  • 21. Falling After Starting Running in a Case of Myoclonus Epilepsy Associated with Ragged-red Fibers with a 8344A>G mtDNA Mutation.
    Miyaue N, Yamanishi Y, Tada S, Ando R, Nagai M, Nomoto M.
    Intern Med; 2018 Dec 01; 57(23):3439-3443. PubMed ID: 29984755
    [Abstract] [Full Text] [Related]

  • 22. Ekbom's syndrome: lipomas, ataxia, and neuropathy with MERRF.
    Calabresi PA, Silvestri G, DiMauro S, Griggs RC.
    Muscle Nerve; 1994 Aug 01; 17(8):943-5. PubMed ID: 8041403
    [Abstract] [Full Text] [Related]

  • 23. Overlapping syndrome of MERRF and MELAS: molecular and neuroradiological studies.
    Chen RS, Huang CC, Lee CC, Wai YY, Hsi MS, Pang CY, Wei YH.
    Acta Neurol Scand; 1993 Jun 01; 87(6):494-8. PubMed ID: 8356881
    [Abstract] [Full Text] [Related]

  • 24. [Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].
    Tanno Y, Yoneda M, Tanaka K, Tsuji S.
    Nihon Rinsho; 1993 Sep 01; 51(9):2379-85. PubMed ID: 8411716
    [Abstract] [Full Text] [Related]

  • 25. The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation.
    Chen HF, Chen CY, Lin TH, Huang ZW, Chi TH, Ma YS, Wu SB, Wei YH, Hsieh M.
    FEBS J; 2012 Aug 01; 279(16):2987-3001. PubMed ID: 22742457
    [Abstract] [Full Text] [Related]

  • 26. Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.
    Ozawa M, Nishino I, Horai S, Nonaka I, Goto YI.
    Muscle Nerve; 1997 Mar 01; 20(3):271-8. PubMed ID: 9052804
    [Abstract] [Full Text] [Related]

  • 27. A Novel Mutation of Mitochondrial T14709C Causes Myoclonic Epilepsy with Ragged Red Fibers Syndrome in a Chinese Patient.
    Ban R, Guo JH, Pu CQ, Shi Q, Liu HX, Zhang YT.
    Chin Med J (Engl); 2018 Jul 05; 131(13):1569-1574. PubMed ID: 29941710
    [Abstract] [Full Text] [Related]

  • 28. MERRF syndrome without ragged-red fibers: the need for molecular diagnosis.
    Mancuso M, Petrozzi L, Filosto M, Nesti C, Rocchi A, Choub A, Pistolesi S, Massetani R, Fontanini G, Siciliano G.
    Biochem Biophys Res Commun; 2007 Mar 23; 354(4):1058-60. PubMed ID: 17275787
    [Abstract] [Full Text] [Related]

  • 29. [Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome].
    Stratilová L, Zeman J, Houst'ková H, Hansíková H, Konrádová V, Hůlková H, Elleder M, Růzicka E, Tyl D, Hrubá E, Houstĕk J.
    Cas Lek Cesk; 1999 Jun 28; 138(13):401-5. PubMed ID: 10566210
    [Abstract] [Full Text] [Related]

  • 30. Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutation.
    Blakely EL, Alston CL, Lecky B, Chakrabarti B, Falkous G, Turnbull DM, Taylor RW, Gorman GS.
    Neuromuscul Disord; 2014 Jun 28; 24(6):533-6. PubMed ID: 24792523
    [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. A case of MERRF associated with chronic pancreatitis.
    Toyono M, Nakano K, Kiuchi M, Imai K, Suzuki H, Shishikura K, Osawa M, Shiratori K, Goto Y, Nonaka I, Sugie H.
    Neuromuscul Disord; 2001 Apr 15; 11(3):300-4. PubMed ID: 11297946
    [Abstract] [Full Text] [Related]

  • 33. Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.
    Altmann J, Büchner B, Nadaj-Pakleza A, Schäfer J, Jackson S, Lehmann D, Deschauer M, Kopajtich R, Lautenschläger R, Kuhn KA, Karle K, Schöls L, Schulz JB, Weis J, Prokisch H, Kornblum C, Claeys KG, Klopstock T.
    J Neurol; 2016 May 15; 263(5):961-972. PubMed ID: 26995359
    [Abstract] [Full Text] [Related]

  • 34. [Two cases of MERRF (myoclonus epilepsy associated with ragged red fibers) showing different clinical features in the same family].
    Nomura T, Ota M, Kotake N, Tanaka K.
    Rinsho Shinkeigaku; 1993 Nov 15; 33(11):1198-200. PubMed ID: 8124882
    [Abstract] [Full Text] [Related]

  • 35. Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR.
    Szuhai K, Ouweland J, Dirks R, Lemaître M, Truffert J, Janssen G, Tanke H, Holme E, Maassen J, Raap A.
    Nucleic Acids Res; 2001 Feb 01; 29(3):E13. PubMed ID: 11160915
    [Abstract] [Full Text] [Related]

  • 36. Impaired ROS Scavenging System in Human Induced Pluripotent Stem Cells Generated from Patients with MERRF Syndrome.
    Chou SJ, Tseng WL, Chen CT, Lai YF, Chien CS, Chang YL, Lee HC, Wei YH, Chiou SH.
    Sci Rep; 2016 Mar 30; 6():23661. PubMed ID: 27025901
    [Abstract] [Full Text] [Related]

  • 37. A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation.
    Herrero-Martín MD, Ayuso T, Tuñón MT, Martín MA, Ruiz-Pesini E, Montoya J.
    J Neurol Neurosurg Psychiatry; 2010 Apr 30; 81(4):471-2. PubMed ID: 20360171
    [No Abstract] [Full Text] [Related]

  • 38. [MERRF (myoclonus epilepsy associated with ragged-red fibers)].
    Goto Y.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr 30; (36):150-2. PubMed ID: 11596350
    [No Abstract] [Full Text] [Related]

  • 39. Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism.
    Masucci JP, Schon EA, King MP.
    Mol Cell Biochem; 1997 Sep 30; 174(1-2):215-9. PubMed ID: 9309690
    [Abstract] [Full Text] [Related]

  • 40. Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome.
    Wu SB, Ma YS, Wu YT, Chen YC, Wei YH.
    Mol Neurobiol; 2010 Jun 30; 41(2-3):256-66. PubMed ID: 20411357
    [Abstract] [Full Text] [Related]

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