130 related articles for article (PubMed ID: 11333748)
1. [Analysis of mutations A3243G, C3256T and mitochondrial deletions in 41 diabetic patients].
Biarnésa J; Rojas I; Fernández-Castañer M; Nunes V; Gómez M; Ricart W
Med Clin (Barc); 2001 Mar; 116(8):292-3. PubMed ID: 11333748
[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. [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]
4. 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; 7(2):246-50. PubMed ID: 11257730
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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; 109(5):283-7. PubMed ID: 11507652
[TBL] [Abstract][Full Text] [Related]
7. Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.
Choo-Kang AT; Lynn S; Taylor GA; Daly ME; Sihota SS; Wardell TM; Chinnery PF; Turnbull DM; Walker M
Diabetes; 2002 Jul; 51(7):2317-20. PubMed ID: 12086967
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus.
Rigoli L; Salpietro DC; Caruso RA; Chiarenza A; Barberi I
Acta Diabetol; 1999 Sep; 36(3):163-7. PubMed ID: 10664322
[TBL] [Abstract][Full Text] [Related]
10. Macular pattern dystrophy associated with a mutation of mitochondrial DNA.
Massin P; Guillausseau PJ; Vialettes B; Paquis V; Orsini F; Grimaldi AD; Gaudric A
Am J Ophthalmol; 1995 Aug; 120(2):247-8. PubMed ID: 7639309
[TBL] [Abstract][Full Text] [Related]
11. Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA.
Tanaka K; Takada Y; Matsunaka T; Yuyama S; Fujino S; Maguchi M; Yamashita S; Yuba I
Intern Med; 2000 Mar; 39(3):249-52. PubMed ID: 10772130
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNA(Leu (UUR))) applied to a Norwegian family with diabetes mellitus and hearing loss.
Akbari M; Skjelbred C; Følling I; Sagen J; Krokan HE
Scand J Clin Lab Invest; 2004 Apr; 64(2):86-92. PubMed ID: 15115244
[TBL] [Abstract][Full Text] [Related]
14. [Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA].
Gál A; Szabó A; Pentelényi K; Pál Z
Orv Hetil; 2008 Aug; 149(34):1593-8. PubMed ID: 18708313
[TBL] [Abstract][Full Text] [Related]
15. 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; 27(6):802-8. PubMed ID: 16788417
[TBL] [Abstract][Full Text] [Related]
16. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
Nagata H; Kumahara K; Tomemori T; Arimoto Y; Isoyama K; Yoshida K; Konno A
J Hum Genet; 2001; 46(10):595-9. PubMed ID: 11587074
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy.
Harrison TJ; Boles RG; Johnson DR; LeBlond C; Wong LJ
Am J Ophthalmol; 1997 Aug; 124(2):217-21. PubMed ID: 9262546
[TBL] [Abstract][Full Text] [Related]
19. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
Xiu L; Zhang Q; Yu B
Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
[TBL] [Abstract][Full Text] [Related]
20. [A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA].
Hoshino S; Tamaoka A; Ohkoshi N; Shoji S; Goto Y
Rinsho Shinkeigaku; 1997 Apr; 37(4):326-30. PubMed ID: 9248343
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
