1004 related articles for article (PubMed ID: 10366077)
1. 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]
2. 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]
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. Retinal pigment epithelial dysfunction in human immunodeficiency virus-infected patients with cytomegalovirus retinitis.
Harrison JM; van Heuven WA
Ophthalmology; 1999 Apr; 106(4):790-7. PubMed ID: 10201604
[TBL] [Abstract][Full Text] [Related]
6. Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.
Michaelides M; Wilkie SE; Jenkins S; Holder GE; Hunt DM; Moore AT; Webster AR
Ophthalmology; 2005 Aug; 112(8):1442-7. PubMed ID: 15953638
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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; 113(2):111-6. PubMed ID: 11775531
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
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; 42(4):485-92. PubMed ID: 10230654
[TBL] [Abstract][Full Text] [Related]
12. [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; 26(1):74-7. PubMed ID: 19199257
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Concentric retinitis pigmentosa: clinicopathologic correlations.
Milam AH; De Castro EB; Smith JE; Tang WX; John SK; Gorin MB; Stone EM; Aguirre GD; Jacobson SG
Exp Eye Res; 2001 Oct; 73(4):493-508. PubMed ID: 11825021
[TBL] [Abstract][Full Text] [Related]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. 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; 31(4):240-3. PubMed ID: 21067488
[TBL] [Abstract][Full Text] [Related]
17. Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family members.
Michaelides M; Jenkins SA; Bamiou DE; Sweeney MG; Davis MB; Luxon L; Bird AC; Rath PP
Arch Ophthalmol; 2008 Mar; 126(3):320-8. PubMed ID: 18332310
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
Renner AB; Kellner U; Cropp E; Preising MN; MacDonald IM; van den Hurk JA; Cremers FP; Foerster MH
Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340
[TBL] [Abstract][Full Text] [Related]
20. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
Newkirk JE; Taylor RW; Howell N; Bindoff LA; Chinnery PF; Alberti KG; Turnbull DM; Walker M
Diabet Med; 1997 Jun; 14(6):457-60. PubMed ID: 9212310
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
