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324 related items for PubMed ID: 10074618

  • 1. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].
    Biarnés J, Barrientos A, Ricart W, Nunes V, Fernández-Castañer M, Soler J.
    Med Clin (Barc); 1999 Jan 30; 112(3):99-101. PubMed ID: 10074618
    [Abstract] [Full Text] [Related]

  • 2. 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 30; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 3. 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 30; 7(2):246-50. PubMed ID: 11257730
    [Abstract] [Full Text] [Related]

  • 4. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
    van den Ouweland JM, Lemkes HH, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PA, van de Kamp JJ, Maassen JA.
    Nat Genet; 1992 Aug 30; 1(5):368-71. PubMed ID: 1284550
    [Abstract] [Full Text] [Related]

  • 5. A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.
    Chen FL, Liu Y, Song XY, Hu HY, Xu HB, Zhang XM, Shi JH, Hu J, Shen Y, Lu B, Wang XC, Hu RM.
    Mutat Res; 2006 Dec 01; 602(1-2):26-33. PubMed ID: 16949108
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 113(2):111-6. PubMed ID: 11775531
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

  • 8. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees].
    Wang CL, Li F, Hou QZ, Li HZ, Zhang Y, Ning G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb 01; 26(1):74-7. PubMed ID: 19199257
    [Abstract] [Full Text] [Related]

  • 9. Level of heteroplasmy for the mitochondrial mutation A3243G correlates with age at onset of diabetes and deafness.
    Olsson C, Zethelius B, Lagerström-Fermér M, Asplund J, Berne C, Landegren U.
    Hum Mutat; 1998 Feb 01; 12(1):52-8. PubMed ID: 9633820
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 01; 14(6):343-8. PubMed ID: 11853367
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 42(4):485-92. PubMed ID: 10230654
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 43(6):746-51. PubMed ID: 7910800
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
    Xiang K, Wang Y, Wu S, Lu H, Zheng T, Sun D, Weng Q, Jia W, Shen W, Pu L, He J.
    Chin Med J (Engl); 1997 May 17; 110(5):372-8. PubMed ID: 9594306
    [Abstract] [Full Text] [Related]

  • 15. 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 17; 15(11):946-52. PubMed ID: 9827849
    [Abstract] [Full Text] [Related]

  • 16. Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus.
    Klemm T, Neumann S, Trülzsch B, Pistrosch F, Hanefeld M, Paschke R.
    Exp Clin Endocrinol Diabetes; 2001 Nov 17; 109(5):283-7. PubMed ID: 11507652
    [Abstract] [Full Text] [Related]

  • 17. Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.
    Lu J, Wang D, Li R, Li W, Ji J, Zhao J, Ye W, Yang L, Qian Y, Zhu Y, Guan MX.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):115-9. PubMed ID: 16876129
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 25(2):127-35. PubMed ID: 19116951
    [Abstract] [Full Text] [Related]

  • 19. Ptosis as an associated finding in maternally inherited diabetes and deafness.
    Robberecht K, Decock C, Stevens A, Seneca S, De Bleecker J, Leroy BP.
    Ophthalmic Genet; 2010 Dec 15; 31(4):240-3. PubMed ID: 21067488
    [Abstract] [Full Text] [Related]

  • 20. [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
    [Abstract] [Full Text] [Related]

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