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Journal Abstract Search

244 related items for PubMed ID: 15794182

  • 21. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW, Huang CC, Tsai JL, Liu JY, Pang CY, Lee HC, Wang EK, Wei YH.
    Acta Neurol Scand; 2000 Jan; 101(1):65-9. PubMed ID: 10660156
    [Abstract] [Full Text] [Related]

  • 22. Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).
    De Kremer RD, Paschini-Capra A, Bacman S, Argaraña C, Civallero G, Kelley RI, Guelbert N, Latini A, Noher de Halac I, Giner-Ayala A, Johnston J, Proujansky R, Gonzalez I, Depetris-Boldini C, Oller-Ramírez A, Angaroni C, Theaux RA, Hliba E, Juaneda E.
    Am J Med Genet; 2001 Mar 01; 99(2):83-93. PubMed ID: 11241464
    [Abstract] [Full Text] [Related]

  • 23. 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 01; 30(8):919-27. PubMed ID: 20656703
    [Abstract] [Full Text] [Related]

  • 24. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
    Degoul F, Diry M, Pou-Serradell A, Lloreta J, Marsac C.
    Ann Neurol; 1994 Mar 01; 35(3):365-70. PubMed ID: 8122891
    [Abstract] [Full Text] [Related]

  • 25. 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 01; 110(11):851-5. PubMed ID: 9772417
    [Abstract] [Full Text] [Related]

  • 26. The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).
    Nishino I, Komatsu M, Kodama S, Horai S, Nonaka I, Goto Y.
    Muscle Nerve; 1996 Dec 01; 19(12):1603-4. PubMed ID: 8941275
    [No Abstract] [Full Text] [Related]

  • 27. Wolff-Parkinson-White syndrome in Patients With MELAS.
    Sproule DM, Kaufmann P, Engelstad K, Starc TJ, Hordof AJ, De Vivo DC.
    Arch Neurol; 2007 Nov 01; 64(11):1625-7. PubMed ID: 17998445
    [Abstract] [Full Text] [Related]

  • 28. Disruption of endothelial tight junctions in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Matsuzaki M, Takahashi R, Nakayama T, Shishikura K, Suzuki H, Hirayama Y, Osawa M, Oda H.
    Neuropediatrics; 2010 Aug 01; 41(2):72-4. PubMed ID: 20799154
    [Abstract] [Full Text] [Related]

  • 29. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.
    Hoptasz M, Szczuciński A, Losy J.
    Neurol Neurochir Pol; 2014 Aug 01; 48(2):150-3. PubMed ID: 24821643
    [Abstract] [Full Text] [Related]

  • 30. MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation.
    Prasad M, Narayan B, Prasad AN, Rupar CA, Levin S, Kronick J, Ramsay D, Tay KY, Prasad C.
    Can J Neurol Sci; 2014 Mar 01; 41(2):210-9. PubMed ID: 24534033
    [Abstract] [Full Text] [Related]

  • 31. Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.
    Demarest ST, Whitehead MT, Turnacioglu S, Pearl PL, Gropman AL.
    J Child Neurol; 2014 Sep 01; 29(9):1249-56. PubMed ID: 25038129
    [Abstract] [Full Text] [Related]

  • 32. Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
    Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB.
    Biochim Biophys Acta; 1995 May 24; 1271(1):135-40. PubMed ID: 7599199
    [Abstract] [Full Text] [Related]

  • 33. Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.
    Huang CC, Kuo HC, Chu CC, Liou CW, Ma YS, Wei YH.
    J Biomed Sci; 2002 May 24; 9(6 Pt 1):527-33. PubMed ID: 12372990
    [Abstract] [Full Text] [Related]

  • 34. Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
    Morovvati S, Nakagawa M, Sato Y, Hamada K, Higuchi I, Osame M.
    Acta Neurol Scand; 2002 Aug 24; 106(2):104-8. PubMed ID: 12100370
    [Abstract] [Full Text] [Related]

  • 35. The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families.
    Vilarinho L, Santorelli FM, Coelho I, Rodrigues L, Maia M, Barata I, Cabral P, Dionísio A, Costa A, Guimarães A, DiMauro S.
    J Neurol Sci; 1999 Mar 01; 163(2):168-74. PubMed ID: 10371079
    [Abstract] [Full Text] [Related]

  • 36. Investigation of common mitochondrial point mutations in Korea.
    Kwon SJ, Park SS, Kim JM, Ahn TB, Kim SH, Kim J, Lee SH, Ha CK, Ahn MY, Jeon BS.
    Ann N Y Acad Sci; 2004 Apr 01; 1011():339-44. PubMed ID: 15126311
    [Abstract] [Full Text] [Related]

  • 37. [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]

  • 38. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.
    Mongini T, Doriguzzi C, Chiadò-Piat L, Silvestri G, Servidei S, Palmucci L.
    Clin Neuropathol; 2002 Dec 07; 21(2):72-6. PubMed ID: 12005255
    [Abstract] [Full Text] [Related]

  • 39. [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 07; 36(11):1159-67. PubMed ID: 25567874
    [Abstract] [Full Text] [Related]

  • 40. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H.
    J Med Genet; 2010 Oct 07; 47(10):659-64. PubMed ID: 20610441
    [Abstract] [Full Text] [Related]

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