243 related articles for article (PubMed ID: 8777986)
1. Maternally inherited diabetes and deafness: a new diabetes subtype.
Maassen JA; Kadowaki T
Diabetologia; 1996 Apr; 39(4):375-82. PubMed ID: 8777986
[TBL] [Abstract][Full Text] [Related]
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; 29(2):50-5. PubMed ID: 9105898
[TBL] [Abstract][Full Text] [Related]
3. 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; 104(3):205-11. PubMed ID: 8817237
[TBL] [Abstract][Full Text] [Related]
4. Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family.
Rigoli L; Prisco F; Caruso RA; Iafusco D; Ursomanno G; Zuccarello D; Ingenito N; Rigoli M; Barberi I
Diabet Med; 2001 Apr; 18(4):334-6. PubMed ID: 11437868
[No Abstract] [Full Text] [Related]
5. Mitochondrial diabetes mellitus.
Rötig A; Bonnefont JP; Munnich A
Diabetes Metab; 1996 Oct; 22(5):291-8. PubMed ID: 8896989
[TBL] [Abstract][Full Text] [Related]
6. 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; 43(6):746-51. PubMed ID: 7910800
[TBL] [Abstract][Full Text] [Related]
7. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
van den Ouweland JM; Lemkes HH; Gerbitz KD; Maassen JA
Muscle Nerve Suppl; 1995; 3():S124-30. PubMed ID: 7603513
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
Katagiri H; Asano T; Ishihara H; Inukai K; Anai M; Yamanouchi T; Tsukuda K; Kikuchi M; Kitaoka H; Ohsawa N
Diabetologia; 1994 May; 37(5):504-10. PubMed ID: 8056189
[TBL] [Abstract][Full Text] [Related]
9. 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; 245(2):523-7. PubMed ID: 9571188
[TBL] [Abstract][Full Text] [Related]
10. [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; 142(5):229-33. PubMed ID: 9557035
[TBL] [Abstract][Full Text] [Related]
11. 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; 602(1-2):26-33. PubMed ID: 16949108
[TBL] [Abstract][Full Text] [Related]
12. HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.
van Essen EH; Roep BO; 't Hart LM; Jansen JJ; Van den Ouweland JM; Lemkes HH; Maassen JA
Diabet Med; 2000 Dec; 17(12):841-7. PubMed ID: 11168326
[TBL] [Abstract][Full Text] [Related]
13. [Mitochondrial diabetes: clinical features, diagnosis and management].
Meas T; Laloi-Michelin M; Virally M; Ambonville C; Kevorkian JP; Guillausseau PJ
Rev Med Interne; 2010 Mar; 31(3):216-21. PubMed ID: 19299044
[TBL] [Abstract][Full Text] [Related]
14. 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; 106(6):1101-8. PubMed ID: 10366077
[TBL] [Abstract][Full Text] [Related]
15. [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; 112(3):99-101. PubMed ID: 10074618
[TBL] [Abstract][Full Text] [Related]
16. Prevalence of maternally inherited diabetes and deafness in Australian diabetic subjects.
Holmes-Walker DJ; Boyages SC
Diabetologia; 1999 Aug; 42(8):1028-9. PubMed ID: 10491766
[No Abstract] [Full Text] [Related]
17. Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
Gerbitz KD; Paprotta A; Jaksch M; Zierz S; Drechsel J
FEBS Lett; 1993 Apr; 321(2-3):194-6. PubMed ID: 8477849
[TBL] [Abstract][Full Text] [Related]
18. 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; 1(5):368-71. PubMed ID: 1284550
[TBL] [Abstract][Full Text] [Related]
19. [Detection of a mutation in mitochondrial DNA in a family with sensorineural deafness and diabetes mellitus as the predominant clinical features].
Tamagawa Y; Tanaka H; Hagiwara H; Ishida T; Kitamura K; Nishizawa M
Nihon Jibiinkoka Gakkai Kaiho; 1995 Jul; 98(7):1104-10. PubMed ID: 7562231
[TBL] [Abstract][Full Text] [Related]
20. 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; 15(11):946-52. PubMed ID: 9827849
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
