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

244 related items for PubMed ID: 9772504

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.
    Biochem Biophys Res Commun; 1998 Apr 17; 245(2):523-7. PubMed ID: 9571188
    [Abstract] [Full Text] [Related]

  • 6. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ, Mudde AH, 't Hart LM, Huygen PL, Cremers CW.
    Otol Neurotol; 2006 Sep 17; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

  • 7. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
    Newkirk JE, Taylor RW, Howell N, Bindoff LA, Chinnery PF, Alberti KG, Turnbull DM, Walker M.
    Diabet Med; 1997 Jun 17; 14(6):457-60. PubMed ID: 9212310
    [Abstract] [Full Text] [Related]

  • 8. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.
    Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, Tanabe Y, Sakura H, Awata T, Goto Y.
    N Engl J Med; 1994 Apr 07; 330(14):962-8. PubMed ID: 8121460
    [Abstract] [Full Text] [Related]

  • 9. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
    Nagata H, Kumahara K, Tomemori T, Arimoto Y, Isoyama K, Yoshida K, Konno A.
    J Hum Genet; 2001 Apr 07; 46(10):595-9. PubMed ID: 11587074
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

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

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 18. Mitochondrial gene mutations that affect the binding of the termination factor and their prevalence among Japanese diabetes mellitus.
    Odawara M, Asano M, Yamashita K.
    Nucleic Acids Symp Ser; 1995 Apr 07; (34):237-8. PubMed ID: 8841639
    [Abstract] [Full Text] [Related]

  • 19. A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern.
    Hosszúfalusi N, Karcagi V, Horváth R, Palik E, Várkonyi J, Rajczy K, Prohászka Z, Szentirmai C, Karádi I, Romics L, Pánczél P.
    Diabetes Metab Res Rev; 2009 Feb 07; 25(2):127-35. PubMed ID: 19116951
    [Abstract] [Full Text] [Related]

  • 20. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun 07; 28(3):332-42. PubMed ID: 17485982
    [Abstract] [Full Text] [Related]

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