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

220 related items for PubMed ID: 9212310

  • 1. 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; 14(6):457-60. PubMed ID: 9212310
    [Abstract] [Full Text] [Related]

  • 2. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus.
    Małecki M, Klupa T, Wanic K, Frey J, Cyganek K, Sieradzki J.
    Med Sci Monit; 2001 Jun; 7(2):246-50. PubMed ID: 11257730
    [Abstract] [Full Text] [Related]

  • 3. 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; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

  • 4. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?
    Holmes-Walker DJ, Mitchell P, Boyages SC.
    Diabet Med; 1998 Nov; 15(11):946-52. PubMed ID: 9827849
    [Abstract] [Full Text] [Related]

  • 5. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 6. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
    Tsukuda K, Suzuki Y, Kameoka K, Osawa N, Goto Y, Katagiri H, Asano T, Yazaki Y, Oka Y.
    Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec; 14(6):343-8. PubMed ID: 11853367
    [Abstract] [Full Text] [Related]

  • 8. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N, Babazono T, Tsuchiya K, Tomonaga O, Suzuki A, Togashi M, Ujihara N, Sakka Y, Yokokawa H, Ogata M, Nihei H, Iwamoto Y.
    J Hum Genet; 2001 Dec; 46(6):330-4. PubMed ID: 11393536
    [Abstract] [Full Text] [Related]

  • 9. Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.
    Katulanda P, Groves CJ, Barrett A, Sheriff R, Matthews DR, McCarthy MI, Gloyn AL.
    Diabet Med; 2008 Mar; 25(3):370-4. PubMed ID: 18279408
    [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. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
    Maassen JA, van den Ouweland JM, t Hart LM, Lemkes HH.
    Horm Metab Res; 1997 Feb; 29(2):50-5. PubMed ID: 9105898
    [Abstract] [Full Text] [Related]

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

  • 15. Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.
    van den Ouweland JM, Maechler P, Wollheim CB, Attardi G, Maassen JA.
    Diabetologia; 1999 Apr; 42(4):485-92. PubMed ID: 10230654
    [Abstract] [Full Text] [Related]

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

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

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

  • 19. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
    van den Ouweland JM, Lemkes HH, Gerbitz KD, Maassen JA.
    Muscle Nerve Suppl; 1995 Apr; 3():S124-30. PubMed ID: 7603513
    [Abstract] [Full Text] [Related]

  • 20. 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]

    Page: [Next] [New Search]
    of 11.