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Journal Abstract Search

121 related items for PubMed ID: 26219939

  • 21. Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.
    Latvala T, Mustonen E, Uusitalo R, Majamaa K.
    Graefes Arch Clin Exp Ophthalmol; 2002 Oct; 240(10):795-801. PubMed ID: 12397426
    [Abstract] [Full Text] [Related]

  • 22. Fear of disease progression in carriers of the m.3243A > G mutation.
    Custers JAE, de Laat P, Koene S, Smeitink J, Janssen MCH, Verhaak C.
    Orphanet J Rare Dis; 2018 Nov 13; 13(1):203. PubMed ID: 30424784
    [Abstract] [Full Text] [Related]

  • 23. Detection rates and phenotypic spectrum of m.3243A>G in the MT-TL1 gene: a molecular diagnostic laboratory perspective.
    Chin J, Marotta R, Chiotis M, Allan EH, Collins SJ.
    Mitochondrion; 2014 Jul 13; 17():34-41. PubMed ID: 24846800
    [Abstract] [Full Text] [Related]

  • 24. Lifestyle Changes Normalize Serum Lactate Levels in an m.3243A>G Carrier.
    Finsterer J.
    Am J Case Rep; 2021 Apr 19; 22():e930175. PubMed ID: 33867519
    [Abstract] [Full Text] [Related]

  • 25. Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.
    Kärppä M, Mahjneh I, Karttunen A, Tolonen U, Majamaa K.
    J Neurol; 2004 May 19; 251(5):556-63. PubMed ID: 15164188
    [Abstract] [Full Text] [Related]

  • 26. MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy level.
    de Wit HM, Westeneng HJ, van Engelen BG, Mudde AH.
    Neth J Med; 2012 Dec 19; 70(10):460-2. PubMed ID: 23230016
    [Abstract] [Full Text] [Related]

  • 27. Cardiac involvement in adults with m.3243A>G MELAS gene mutation.
    Vydt TC, de Coo RF, Soliman OI, Ten Cate FJ, van Geuns RJ, Vletter WB, Schoonderwoerd K, van den Bosch BJ, Smeets HJ, Geleijnse ML.
    Am J Cardiol; 2007 Jan 15; 99(2):264-9. PubMed ID: 17223431
    [Abstract] [Full Text] [Related]

  • 28. Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M, Syrjälä P, Tolonen U, Majamaa K.
    J Neurol; 2003 Feb 15; 250(2):216-21. PubMed ID: 12574954
    [Abstract] [Full Text] [Related]

  • 29. Head lifting strength is associated with dysphagia and malnutrition in frail older adults.
    Wakabayashi H, Sashika H, Matsushima M.
    Geriatr Gerontol Int; 2015 Apr 15; 15(4):410-6. PubMed ID: 24690326
    [Abstract] [Full Text] [Related]

  • 30. [Mitochondrial genome analysis in the probands of six Chinese families with MELAS].
    Liu L, Yuquan S, Baorong Z, Pingping J, Ailian D, Minxin G.
    Yi Chuan; 2014 Nov 15; 36(11):1159-67. PubMed ID: 25567874
    [Abstract] [Full Text] [Related]

  • 31. Mitochondrial DNA mutation m.3243A>G is associated with altered mitochondrial function in peripheral blood mononuclear cells, with heteroplasmy levels and with clinical phenotypes.
    Geng X, Zhang Y, Yan J, Chu C, Gao F, Jiang Z, Zhang X, Chen Y, Wei X, Feng Y, Lu H, Wang C, Zeng F, Jia W.
    Diabet Med; 2019 Jun 15; 36(6):776-783. PubMed ID: 30536471
    [Abstract] [Full Text] [Related]

  • 32. The urinary proteome and metabonome differ from normal in adults with mitochondrial disease.
    Hall AM, Vilasi A, Garcia-Perez I, Lapsley M, Alston CL, Pitceathly RD, McFarland R, Schaefer AM, Turnbull DM, Beaumont NJ, Hsuan JJ, Cutillas PR, Lindon JC, Holmes E, Unwin RJ, Taylor RW, Gorman GS, Rahman S, Hanna MG.
    Kidney Int; 2015 Mar 15; 87(3):610-22. PubMed ID: 25207879
    [Abstract] [Full Text] [Related]

  • 33. Pre-eclampsia and magnesium toxicity with therapeutic plasma level in a woman with m.3243A>G melas mutation.
    Moriarty KT, McFarland R, Whittaker R, Burch J, Turnbull HE, Taylor RW, Turnbull DM.
    J Obstet Gynaecol; 2008 Apr 15; 28(3):349. PubMed ID: 18569490
    [No Abstract] [Full Text] [Related]

  • 34. Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
    Marotta R, Reardon K, McKelvie PA, Chiotis M, Chin J, Cook M, Collins SJ.
    J Clin Neurosci; 2009 Sep 15; 16(9):1223-5. PubMed ID: 19502062
    [Abstract] [Full Text] [Related]

  • 35. High prevalence of impaired glucose homeostasis and myopathy in asymptomatic and oligosymptomatic 3243A>G mitochondrial DNA mutation-positive subjects.
    Frederiksen AL, Jeppesen TD, Vissing J, Schwartz M, Kyvik KO, Schmitz O, Poulsen PL, Andersen PH.
    J Clin Endocrinol Metab; 2009 Aug 15; 94(8):2872-9. PubMed ID: 19470628
    [Abstract] [Full Text] [Related]

  • 36. Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A > G tRNA(Leu) mutation.
    van Eijsden RG, Eijssen LM, Lindsey PJ, van den Burg CM, de Wit LE, Rubio-Gozalbo ME, de Die CE, Ayoubi T, Sluiter W, de Coo IF, Smeets HJ.
    J Med Genet; 2008 Aug 15; 45(8):525-34. PubMed ID: 18456717
    [Abstract] [Full Text] [Related]

  • 37. High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.
    Cevoli S, Pallotti F, La Morgia C, Valentino ML, Pierangeli G, Cortelli P, Baruzzi A, Montagna P, Carelli V.
    Cephalalgia; 2010 Aug 15; 30(8):919-27. PubMed ID: 20656703
    [Abstract] [Full Text] [Related]

  • 38. Postlingual hearing loss as a mitochondrial 3243A>G mutation phenotype.
    Iwanicka-Pronicka K, Pollak A, Skórka A, Lechowicz U, Pajdowska M, Furmanek M, Rzeski M, Korniszewski L, Skarżyński H, Płoski R.
    PLoS One; 2012 Aug 15; 7(10):e44054. PubMed ID: 23133508
    [Abstract] [Full Text] [Related]

  • 39. Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation.
    Hsiue HC, Lee NC, Tsai HB, Yang CC, Wu CS, Lee WT, Weng WC, Fan PC, Chien YH, Hwu WL, Hung KL, Huang CC, Chen CH, Lin SJ, Chu SY, Wang TJ, Lu CJ, Lee PL.
    Intensive Care Med; 2015 Aug 15; 41(8):1493-5. PubMed ID: 26077074
    [No Abstract] [Full Text] [Related]

  • 40. Gastrointestinal involvement is frequent in Myotonic Dystrophy type 2.
    Tieleman AA, van Vliet J, Jansen JB, van der Kooi AJ, Borm GF, van Engelen BG.
    Neuromuscul Disord; 2008 Aug 15; 18(8):646-9. PubMed ID: 18602828
    [Abstract] [Full Text] [Related]

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