These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

247 related items for PubMed ID: 18314141

  • 21. 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]

  • 22. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov; 122(11):978-81. PubMed ID: 9822126
    [Abstract] [Full Text] [Related]

  • 23. Cell cycle of myocytes of cardiac and skeletal muscle in mitochondrial myopathy.
    Takeda A, Chiba S, Takaaki I, Tanamura A, Yamaguchi Y, Takeda N.
    Jpn Circ J; 1998 Sep; 62(9):695-9. PubMed ID: 9766710
    [Abstract] [Full Text] [Related]

  • 24. Late onset of stroke-like episode associated with a 3256C-->T point mutation of mitochondrial DNA.
    Jeppesen TD, Schwartz M, Hansen K, Danielsen ER, Wibrand F, Vissing J.
    J Neurol Sci; 2003 Oct 15; 214(1-2):17-20. PubMed ID: 12972383
    [Abstract] [Full Text] [Related]

  • 25. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
    Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R.
    Arch Neurol; 2004 Feb 15; 61(2):269-72. PubMed ID: 14967777
    [Abstract] [Full Text] [Related]

  • 26. A study of familial MELAS: evaluation of A3243G mutation, clinical phenotype, and magnetic resonance spectroscopy-monitored progression.
    Chen C, Xiong N, Wang Y, Xiong J, Huang J, Zhang Z, Wang T.
    Neurol India; 2012 Feb 15; 60(1):86-9. PubMed ID: 22406788
    [Abstract] [Full Text] [Related]

  • 27. 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 15; 110(11):851-5. PubMed ID: 9772417
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. MELAS syndrome associated with a tandem duplication in the D-loop of mitochondrial DNA.
    Li JY, Kong KW, Chang MH, Cheung SC, Lee HC, Pang CY, Wei YH.
    Acta Neurol Scand; 1996 Jun 15; 93(6):450-5. PubMed ID: 8836308
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun 15; 43(6):746-51. PubMed ID: 7910800
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes.
    Li R, Guan MX.
    Mol Cell Biol; 2010 May 15; 30(9):2147-54. PubMed ID: 20194621
    [Abstract] [Full Text] [Related]

  • 36. An 80-year-old mitochondrial disease patient with A3243G tRNA(Leu(UUR)) gene presenting cardiac dysfunction as the main symptom.
    Higashikata T, Koyama J, Shimada H, Yazaki M, Owa M, Ikeda S.
    Intern Med; 2001 May 15; 40(5):405-8. PubMed ID: 11393411
    [Abstract] [Full Text] [Related]

  • 37. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ, Lertrit P, Berkovic SF, Crimmins D, Morris J, Marzuki S, Byrne E.
    Aust N Z J Med; 1994 Apr 15; 24(2):188-93. PubMed ID: 8042948
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep 15; 4(5):631-44. PubMed ID: 15347257
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.