232 related articles for article (PubMed ID: 28599824)
21. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
Iwasaki N; Babazono T; Tsuchiya K; Tomonaga O; Suzuki A; Togashi M; Ujihara N; Sakka Y; Yokokawa H; Ogata M; Nihei H; Iwamoto Y
J Hum Genet; 2001; 46(6):330-4. PubMed ID: 11393536
[TBL] [Abstract][Full Text] [Related]
22. Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD).
Narbonne H; Paquis-Fluckinger V; Valero R; Heyries L; Pellissier JF; Vialettes B
Diabetes Metab; 2004 Feb; 30(1):61-6. PubMed ID: 15029099
[TBL] [Abstract][Full Text] [Related]
23. Prevalence and risk factors for diabetic retinopathy in Asian Indians with young onset type 1 and type 2 diabetes.
Rajalakshmi R; Amutha A; Ranjani H; Ali MK; Unnikrishnan R; Anjana RM; Narayan KM; Mohan V
J Diabetes Complications; 2014; 28(3):291-7. PubMed ID: 24512748
[TBL] [Abstract][Full Text] [Related]
24. Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea.
Rho EH; Baek SI; Lee H; Seong MW; Chae JH; Park KS; Kwak SH
Diabetes Metab J; 2024 May; 48(3):482-486. PubMed ID: 38311059
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. The urinary proteome and metabonome differ from normal in adults with mitochondrial disease.
Hall AM; Vilasi A; Garcia-Perez I; Lapsley M; Alston CL; Pitceathly RD; McFarland R; Schaefer AM; Turnbull DM; Beaumont NJ; Hsuan JJ; Cutillas PR; Lindon JC; Holmes E; Unwin RJ; Taylor RW; Gorman GS; Rahman S; Hanna MG
Kidney Int; 2015 Mar; 87(3):610-22. PubMed ID: 25207879
[TBL] [Abstract][Full Text] [Related]
27. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
Suzuki S; Hinokio Y; Ohtomo M; Hirai M; Hirai A; Chiba M; Kasuga S; Satoh Y; Akai H; Toyota T
Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
[TBL] [Abstract][Full Text] [Related]
28. [A 20-year prospective follow-up study to evaluate the development of retinopathy and nephropathy after the onset of type 1 diabetes mellitus: Contribution of glycemic control and metabolic memory].
Bolotskaya LL; Bessmertnaya EG; Shestakova MV; Shamkhalova MS; Nikankina LV; Ilyin AV; Glek IS; Zolotukhin AV; Dedov II
Ter Arkh; 2017; 89(10):17-21. PubMed ID: 29171465
[TBL] [Abstract][Full Text] [Related]
29. Identification of eight genomic protective alleles for mitochondrial diabetes by Kinship-graph convolutional network.
Wang J; Yan D; Cui H; Zhang R; Ma X; Chen L; Hu C; Wu J
J Diabetes Investig; 2024 Jan; 15(1):52-62. PubMed ID: 38157301
[TBL] [Abstract][Full Text] [Related]
30. Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report.
Sugai K; Ueda H; Morimoto K; Tanaka M; Takahashi D; Nakashima A; Kato J; Takahashi H; Yamaguchi Y; Kawamura T; Hanaoka K; Miyazaki Y; Yokoo T
BMC Nephrol; 2018 Dec; 19(1):350. PubMed ID: 30526529
[TBL] [Abstract][Full Text] [Related]
31. Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation.
Brändle M; Lehmann R; Maly FE; Schmid C; Spinas GA
Diabetes Care; 2001 Jul; 24(7):1253-8. PubMed ID: 11423511
[TBL] [Abstract][Full Text] [Related]
32. The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
Laloi-Michelin M; Meas T; Ambonville C; Bellanné-Chantelot C; Beaufils S; Massin P; Vialettes B; Gin H; Timsit J; Bauduceau B; Bernard L; Bertin E; Blickle JF; Cahen-Varsaux J; Cailleba A; Casanova S; Cathebras P; Charpentier G; Chedin P; Crea T; Delemer B; Dubois-Laforgue D; Duchemin F; Ducluzeau PH; Bouhanick B; Dusselier L; Gabreau T; Grimaldi A; Guerci B; Jacquin V; Kaloustian E; Larger E; Lecleire-Collet A; Lorenzini F; Louis J; Mausset J; Murat A; Nadler-Fluteau S; Olivier F; Paquis-Flucklinger V; Paris-Bockel D; Raynaud I; Reznik Y; Riveline JP; Schneebeli S; Sonnet E; Sola-Gazagnes A; Thomas JL; Trabulsi B; Virally M; Guillausseau PJ;
J Clin Endocrinol Metab; 2009 Aug; 94(8):3025-30. PubMed ID: 19470619
[TBL] [Abstract][Full Text] [Related]
33. Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.
Mory PB; Santos MC; Kater CE; Moisés RS
Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):574-7. PubMed ID: 23295301
[TBL] [Abstract][Full Text] [Related]
34. Incidence of complications in young-onset diabetes: Comparing type 2 with type 1 (the young diab study).
Amutha A; Anjana RM; Venkatesan U; Ranjani H; Unnikrishnan R; Narayan KMV; Mohan V; Ali MK
Diabetes Res Clin Pract; 2017 Jan; 123():1-8. PubMed ID: 27912129
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.
Yang M; Xu L; Xu C; Cui Y; Jiang S; Dong J; Liao L
Front Endocrinol (Lausanne); 2021; 12():728043. PubMed ID: 34899594
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Chronological change of left ventricular global longitudinal strain in patients with maternally inherited diabetes and deafness: A case series.
Seo JS
Medicine (Baltimore); 2024 Mar; 103(10):e37447. PubMed ID: 38457558
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcome.
de Laat P; Fleuren LH; Bekker MN; Smeitink JA; Janssen MC
Mitochondrion; 2015 Nov; 25():98-103. PubMed ID: 26455484
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
