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Journal Abstract Search

205 related items for PubMed ID: 11757250

  • 1. [From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
    Leys AM, de Jong PT.
    Ned Tijdschr Geneeskd; 2001 Nov 17; 145(46):2250-2. PubMed ID: 11757250
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  • 2. 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 17; 29(2):50-5. PubMed ID: 9105898
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  • 3. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 17; 14(6):343-8. PubMed ID: 11853367
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  • 4. 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 Dec 17; 106(5):384-8. PubMed ID: 9831303
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  • 8. 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 17; 25(2):127-35. PubMed ID: 19116951
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  • 9. Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family.
    Schleiffer T, 't Hart LM, Schürfeld C, Kraatz K, Riemann JF.
    Exp Clin Endocrinol Diabetes; 2000 Feb 17; 108(2):81-5. PubMed ID: 10826513
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  • 11. The molecular basis and clinical characteristics of Maternally Inherited Diabetes and Deafness (MIDD), a recently recognized diabetic subtype.
    Maassen JA, Jansen JJ, Kadowaki T, van den Ouweland JM, 't Hart LM, Lemkes HH.
    Exp Clin Endocrinol Diabetes; 1996 Feb 17; 104(3):205-11. PubMed ID: 8817237
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  • 17. Mitochondrial DNA (mtDNA) A 3243G mutation associated with an annular perimacular retinal atrophy.
    Adjadj E, Mansouri K, Borruat FX.
    Klin Monbl Augenheilkd; 2008 May 17; 225(5):462-4. PubMed ID: 18454399
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  • 20. New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome.
    Maassen JA, Jahangir Tafrechi RS, Janssen GM, Raap AK, Lemkes HH, 't Hart LM.
    Endocrinol Metab Clin North Am; 2006 Jun 17; 35(2):385-96, x-xi. PubMed ID: 16632100
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