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

Journal Abstract Search


484 related items for PubMed ID: 17484047

  • 1. Mitochondrial DNA medicine.
    DiMauro S.
    Biosci Rep; 2007 Jun; 27(1-3):5-9. PubMed ID: 17484047
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Lessons from mitochondrial DNA mutations.
    DiMauro S.
    Semin Cell Dev Biol; 2001 Dec; 12(6):397-405. PubMed ID: 11735374
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial DNA-related disorders.
    Mancuso M, Filosto M, Choub A, Tentorio M, Broglio L, Padovani A, Siciliano G.
    Biosci Rep; 2007 Jun; 27(1-3):31-7. PubMed ID: 17484046
    [Abstract] [Full Text] [Related]

  • 5. Diseases of oxidative phosphorylation due to mtDNA mutations.
    DiMauro S, Andreu AL, Musumeci O, Bonilla E.
    Semin Neurol; 2001 Sep; 21(3):251-60. PubMed ID: 11641815
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial DNA and disease.
    Dimauro S, Davidzon G.
    Ann Med; 2005 Sep; 37(3):222-32. PubMed ID: 16019721
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [Diseases of the human mitochondrial oxidative phosphorylation system].
    Ruiz-Pesini E, López-Gallardo E, Dahmani Y, Herrero MD, Solano A, Díez-Sánchez C, López-Pérez M, Montoya J.
    Rev Neurol; 2005 Sep; 43(7):416-24. PubMed ID: 17006861
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial DNA analysis in clinical laboratory diagnostics.
    Wong LJ, Boles RG.
    Clin Chim Acta; 2005 Apr; 354(1-2):1-20. PubMed ID: 15748595
    [Abstract] [Full Text] [Related]

  • 11. Autosomal disorders of mitochondrial DNA maintenance.
    Van Goethem G.
    Acta Neurol Belg; 2006 Jun; 106(2):66-72. PubMed ID: 16898256
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. [The mitochondrial genome and human mitochondrial diseases].
    Sukernik RI, Derbeneva OA, Starikovskaia EB, Volod'ko NV, Mikhaĭlovskaia IE, Bychkov IIu, Lott M, Brown M, Wallace D.
    Genetika; 2002 Feb; 38(2):161-70. PubMed ID: 11898607
    [Abstract] [Full Text] [Related]

  • 15. [Mitochondrial disorders: a classification for the 21st century].
    Andreu AL, Gonzalo-Sanz R.
    Neurologia; 2004 Feb; 19(1):15-22. PubMed ID: 14762729
    [Abstract] [Full Text] [Related]

  • 16. Molecular genetic and clinical aspects of mitochondrial disorders in childhood.
    Moslemi AR, Darin N.
    Mitochondrion; 2007 Jul; 7(4):241-52. PubMed ID: 17376748
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation.
    Finsterer J.
    Acta Neurol Scand; 2007 Jul; 116(1):1-14. PubMed ID: 17587249
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 25.