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Journal Abstract Search

218 related items for PubMed ID: 23295301

  • 1.
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  • 2. De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome.
    Jiang Z, Zhang Y, Yan J, Li F, Geng X, Lu H, Wei X, Feng Y, Wang C, Jia W.
    J Diabetes Res; 2019; 2019():5184647. PubMed ID: 31143779
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  • 3. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
    Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH.
    Ned Tijdschr Geneeskd; 1998 Jan 31; 142(5):229-33. PubMed ID: 9557035
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  • 5. Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.
    Bergamin CS, Rolim LC, Dib SA, Moisés RS.
    Arq Bras Endocrinol Metabol; 2008 Nov 31; 52(8):1345-9. PubMed ID: 19169492
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  • 7. 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 31; 106(9):1821-7. PubMed ID: 10485557
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  • 8. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun 31; 43(6):746-51. PubMed ID: 7910800
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  • 9. A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions.
    Mezghani N, Mnif M, Mkaouar-Rebai E, Kallel N, Charfi N, Abid M, Fakhfakh F.
    Biochem Biophys Res Commun; 2013 Feb 22; 431(4):670-4. PubMed ID: 23357420
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  • 11. Chronological change of left ventricular global longitudinal strain in patients with maternally inherited diabetes and deafness: A case series.
    Seo JS.
    Medicine (Baltimore); 2024 Mar 08; 103(10):e37447. PubMed ID: 38457558
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  • 12. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S, Hinokio Y, Ohtomo M, Hirai M, Hirai A, Chiba M, Kasuga S, Satoh Y, Akai H, Toyota T.
    Diabetologia; 1998 May 08; 41(5):584-8. PubMed ID: 9628277
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  • 13. 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 08; 70(10):460-2. PubMed ID: 23230016
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  • 14. Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
    Tabebi M, Charfi N, Kallabi F, Alila-Fersi O, Ben Mahmoud A, Tlili A, Keskes-Ammar L, Kamoun H, Abid M, Mnif M, Fakhfakh F.
    J Diabetes Complications; 2017 Jan 08; 31(1):253-259. PubMed ID: 27422531
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  • 15. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.
    Murphy R, Turnbull DM, Walker M, Hattersley AT.
    Diabet Med; 2008 Apr 08; 25(4):383-99. PubMed ID: 18294221
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  • 16. 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 08; 29(2):50-5. PubMed ID: 9105898
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  • 17. 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 Feb 08; 28(4):542-6. PubMed ID: 24746802
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  • 19. 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 08; 104(3):205-11. PubMed ID: 8817237
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