126 related articles for article (PubMed ID: 16540924)
21. [From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
Leys AM; de Jong PT
Ned Tijdschr Geneeskd; 2001 Nov; 145(46):2250-2. PubMed ID: 11757250
[No Abstract] [Full Text] [Related]
22. Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.
Schrijver I; Gardner P
Expert Rev Mol Diagn; 2006 May; 6(3):375-86. PubMed ID: 16706740
[TBL] [Abstract][Full Text] [Related]
23. [Optic atrophy, type I diabetes and neurosensory hearing loss: a family syndrome].
Bujara K; Burck U; Dreyer M; Koepp P; Herberhold C
Klin Monbl Augenheilkd; 1982 Jun; 180(6):559-62. PubMed ID: 6890123
[No Abstract] [Full Text] [Related]
24. Bilateral versus unilateral sudden sensorineural hearing loss.
Oh JH; Park K; Lee SJ; Shin YR; Choung YH
Otolaryngol Head Neck Surg; 2007 Jan; 136(1):87-91. PubMed ID: 17210340
[TBL] [Abstract][Full Text] [Related]
25. [Dilated cardiomyopathy, diabetes and deafness related to a mutation of mitochondrial DNA].
Ferreira-Maldent N; Maillot F; Quilliet L; Guilmot JL; Charbonnier B
Arch Mal Coeur Vaiss; 2007 Feb; 100(2):149-52. PubMed ID: 17474502
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutation.
Jeppesen TD; Schwartz M; Frederiksen AL; Wibrand F; Olsen DB; Vissing J
Arch Neurol; 2006 Dec; 63(12):1701-6. PubMed ID: 17172609
[TBL] [Abstract][Full Text] [Related]
28. A case of diabetes, deafness, cardiomyopathy, and central sleep apnea: novel mitochondrial DNA polymorphisms.
Sakaue S; Ohmuro J; Mishina T; Miyazaki H; Yamaguchi E; Nishimura M; Fujita M; Nagashima K; Tagami S; Kawakami Y
Tohoku J Exp Med; 2002 Mar; 196(3):203-11. PubMed ID: 12002277
[TBL] [Abstract][Full Text] [Related]
29. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
30. Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNA.
DiFabio R; Santorelli FM; Nola G; Cricchi F; Masi R; Ingrosso A; Fattori F; Carrozzo R; Vanacore N; Pierelli F; Ralli G; Casali C
Neuromuscul Disord; 2009 Apr; 19(4):291-6. PubMed ID: 19233651
[TBL] [Abstract][Full Text] [Related]
31. [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]
32. Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss.
Gold M; Rapin I
Int J Pediatr Otorhinolaryngol; 1994 Aug; 30(2):91-104. PubMed ID: 8063504
[TBL] [Abstract][Full Text] [Related]
33. 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; 348(1):115-9. PubMed ID: 16876129
[TBL] [Abstract][Full Text] [Related]
34. A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea.
De Block CE; De Leeuw IH; Maassen JA; Ballaux D; Martin JJ
Exp Clin Endocrinol Diabetes; 2004 Feb; 112(2):80-3. PubMed ID: 15031771
[TBL] [Abstract][Full Text] [Related]
35. [Clinical manifestation of diabetes from mitochondrial cytopathy].
Vialettes B; Narbonne H; Silvestre-Aillaud P; Bendahan D; Paquis-Flucklinger V
Journ Annu Diabetol Hotel Dieu; 1997; ():17-23. PubMed ID: 9296972
[No Abstract] [Full Text] [Related]
36. A case of mitochondrial diabetes associated with 3243 bp tRNA(Leu(UUR)) mutation with few complications, regardless of 16-year disease duration.
Suzuki Y; Atumi Y; Matsuoka K; Taniyama M; Shigeo O
Diabetes Res Clin Pract; 2005 Sep; 69(3):309-10. PubMed ID: 15913828
[No Abstract] [Full Text] [Related]
37. Genetic factors related to mitochondrial function and risk of diabetes mellitus.
Cho YM; Park KS; Lee HK
Diabetes Res Clin Pract; 2007 Sep; 77 Suppl 1():S172-7. PubMed ID: 17451836
[TBL] [Abstract][Full Text] [Related]
38. Immunohistochemical and ultrastructural abnormalities in muscle from a patient with sensorineural hearing loss related to a 1555 A-to-G mitochondrial mutation.
Kouzaki H; Suzuki M; Shimizu T
J Clin Neurosci; 2007 Jun; 14(6):603-7. PubMed ID: 16935512
[TBL] [Abstract][Full Text] [Related]
39. [How to treat and manage mitochondrial diabetes].
Vialettes B; Narbonne H
Journ Annu Diabetol Hotel Dieu; 2001; ():179-84. PubMed ID: 11565460
[No Abstract] [Full Text] [Related]
40. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.
Uusimaa J; Moilanen JS; Vainionpää L; Tapanainen P; Lindholm P; Nuutinen M; Löppönen T; Mäki-Torkko E; Rantala H; Majamaa K
Ann Neurol; 2007 Sep; 62(3):278-87. PubMed ID: 17823937
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]