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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

386 related items for PubMed ID: 11257730

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  • 22. 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
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  • 25. Molecular and clinical aspects of mitochondrial diabetes mellitus.
    Maassen JA, van Essen E, van den Ouweland JM, Lemkes HH.
    Exp Clin Endocrinol Diabetes; 2001 Dec; 109(3):127-34. PubMed ID: 11409293
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  • 31. 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 Dec; 46(10):595-9. PubMed ID: 11587074
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  • 33. 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
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  • 37. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation.
    Thorns C, Widjaja A, Boeck N, Skamira C, Zühlke H.
    Exp Clin Endocrinol Diabetes; 1998 Mar; 106(5):384-8. PubMed ID: 9831303
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  • 39. 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
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  • 40. Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis.
    Löwik MM, Hol FA, Steenbergen EJ, Wetzels JF, van den Heuvel LP.
    Nephrol Dial Transplant; 2005 Feb 17; 20(2):336-41. PubMed ID: 15585516
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