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

180 related items for PubMed ID: 12923421

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS, Brown DJ, McMillan PM, Barker SE, Lesperance MM.
    Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):830-5. PubMed ID: 12925340
    [Abstract] [Full Text] [Related]

  • 25. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
    Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM.
    Biochem Biophys Res Commun; 2008 Apr 11; 368(3):631-6. PubMed ID: 18261986
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis.
    Maassen JA.
    Am J Med Genet; 2002 May 30; 115(1):66-70. PubMed ID: 12116179
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 34. Long-lived C. elegans mitochondrial mutants as a model for human mitochondrial-associated diseases.
    Ventura N, Rea SL, Testi R.
    Exp Gerontol; 2006 Oct 30; 41(10):974-91. PubMed ID: 16945497
    [Abstract] [Full Text] [Related]

  • 35. Mitochondrial hepatopathies.
    Bandyopadhyay SK, Dutta A.
    J Assoc Physicians India; 2005 Nov 30; 53():973-8. PubMed ID: 16515238
    [Abstract] [Full Text] [Related]

  • 36. Mitochondrial RNA processing and translation: link between mitochondrial mutations and hearing loss?
    Fischel-Ghodsian N.
    Mol Genet Metab; 1998 Oct 30; 65(2):97-104. PubMed ID: 9787101
    [No Abstract] [Full Text] [Related]

  • 37. [Familial neural mitochondrial deafness].
    Marangos N, Mausolf A.
    HNO; 1990 Sep 30; 38(9):322-5. PubMed ID: 2262349
    [Abstract] [Full Text] [Related]

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

  • 39. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
    Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):200-5. PubMed ID: 16875663
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.