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

777 related items for PubMed ID: 12903032

  • 1. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
    Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
    [Abstract] [Full Text] [Related]

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

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. CPEO and KSS differ in the percentage and location of the mtDNA deletion.
    López-Gallardo E, López-Pérez MJ, Montoya J, Ruiz-Pesini E.
    Mitochondrion; 2009 Sep; 9(5):314-7. PubMed ID: 19410662
    [Abstract] [Full Text] [Related]

  • 5. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ, Lopez Gallardo E, Solano A, Dahmani Y, Herrero MD, Montoya J.
    Neurologia; 2006 Sep; 21(7):357-64. PubMed ID: 16977556
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 8. Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population.
    Remes AM, Majamaa-Voltti K, Kärppä M, Moilanen JS, Uimonen S, Helander H, Rusanen H, Salmela PI, Sorri M, Hassinen IE, Majamaa K.
    Neurology; 2005 Mar 22; 64(6):976-81. PubMed ID: 15781811
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Deletion screening of mitochondrial DNA via multiprimer DNA amplification.
    Ernst BP, Wilichowski E, Wagner M, Hanefeld F.
    Mol Cell Probes; 1994 Feb 22; 8(1):45-9. PubMed ID: 8028607
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. [Chronic progressive external ophthalmoplegia (CPEO), Kearns-Sayre syndrome (KSS)].
    Ishikawa H, Nishino I.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb 22; (36):153-6. PubMed ID: 11596351
    [No Abstract] [Full Text] [Related]

  • 13. Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
    Zanssen S, Molnar M, Buse G, Schröder JM.
    Clin Neuropathol; 1998 Feb 22; 17(6):291-6. PubMed ID: 9832255
    [Abstract] [Full Text] [Related]

  • 14. [Chronic progressive external ophthalmoplegia (CPEO); mitochondrial DNA deletion, brain MRI and electrophysiological studies].
    Nakagawa M, Tokimura M, Kuriyama M, Higuchi I, Osame M.
    Rinsho Shinkeigaku; 1991 Sep 22; 31(9):981-6. PubMed ID: 1769162
    [Abstract] [Full Text] [Related]

  • 15. [Chronic progressive external ophthalmoplegia--symptom or syndrome?].
    Bau V, Deschauer M, Zierz S.
    Klin Monbl Augenheilkd; 2009 Oct 22; 226(10):822-8. PubMed ID: 19830638
    [Abstract] [Full Text] [Related]

  • 16. A novel heteroplasmic tRNA(Leu(CUN)) mtDNA point mutation associated with chronic progressive external ophthalmoplegia.
    Cardaioli E, Da Pozzo P, Radi E, Dotti MT, Federico A.
    Biochem Biophys Res Commun; 2005 Feb 18; 327(3):675-8. PubMed ID: 15649400
    [Abstract] [Full Text] [Related]

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

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

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 39.