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Journal Abstract Search

270 related items for PubMed ID: 9557035

  • 21. 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; 108(2):81-5. PubMed ID: 10826513
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  • 22. Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group.
    Massin P, Virally-Monod M, Vialettes B, Paques M, Gin H, Porokhov B, Caillat-Zucman S, Froguel P, Paquis-Fluckinger V, Gaudric A, Guillausseau PJ.
    Ophthalmology; 1999 Sep; 106(9):1821-7. PubMed ID: 10485557
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  • 23. 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 Sep; 7(2):246-50. PubMed ID: 11257730
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  • 24. 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 Sep; 106(5):384-8. PubMed ID: 9831303
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  • 25. [From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
    Maassen JA, van den Ouweland JM, Losekoot M, Lemkes HH.
    Ned Tijdschr Geneeskd; 2001 Jun 16; 145(24):1153-4. PubMed ID: 11433662
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  • 26. MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy level.
    de Wit HM, Westeneng HJ, van Engelen BG, Mudde AH.
    Neth J Med; 2012 Dec 16; 70(10):460-2. PubMed ID: 23230016
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  • 27. Maternally inherited diabetes and deafness (MIDD): diagnosis and management.
    Naing A, Kenchaiah M, Krishnan B, Mir F, Charnley A, Egan C, Bano G.
    J Diabetes Complications; 2014 Dec 16; 28(4):542-6. PubMed ID: 24746802
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  • 30. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L, Wang H, Chen J, Jin W, Liu L, Ban B, Shen J, Hua Z, Chai J.
    Chin Med J (Engl); 2000 Feb 16; 113(2):111-6. PubMed ID: 11775531
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  • 33. Clinical aspects of mitochondrial diabetes.
    Vialettes B, Paquis-Flucklinger V, Bendahan D.
    Diabetes Metab; 1997 Mar 16; 23 Suppl 2():52-6. PubMed ID: 9105784
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  • 34. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
    Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC.
    Nat Genet; 1992 Apr 16; 1(1):11-5. PubMed ID: 1301992
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  • 36. 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
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