These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. [A case of 3243 point mutation of mitochondrial gene with diabetes mellitus treated with large dose of coenzyme Q]. Usui T; Sawa S; Inoue A; Asahi Y; Takada Y; Ozumi S; Kobayashi T Nihon Naika Gakkai Zasshi; 1995 Nov; 84(11):1904-6. PubMed ID: 8568391 [No Abstract] [Full Text] [Related]
7. Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness. Manouvrier S; Rötig A; Hannebique G; Gheerbrandt JD; Royer-Legrain G; Munnich A; Parent M; Grünfeld JP; Largilliere C; Lombes A J Med Genet; 1995 Aug; 32(8):654-6. PubMed ID: 7473662 [TBL] [Abstract][Full Text] [Related]
8. Short stature is common feature of mitochondrial gene abnormalities with diabetes. Kameoka K; Isotani H; Kitaoka H; Takamatsu J; Ohsawa N Horm Metab Res; 2000 Apr; 32(4):159-60. PubMed ID: 10824714 [No Abstract] [Full Text] [Related]
9. [Diabetes mellitus with mitochondrial DNA tRNA(Leu)(UUR) mutation at 3264(T-->C)]. Suzuki Y; Suzuki S Nihon Rinsho; 1998 Jan; 56 Suppl 3():534-8. PubMed ID: 9513475 [No Abstract] [Full Text] [Related]
10. Cardiac sympathetic nervous dysfunction in mitochondrial cardiomyopathy and diabetes. Ishida Y; Ueno H; Yoshida R; Hozumi T; Shiotani H; Matsunaga K; Kasuga M; Kazumi T Diabetes Care; 1995 Sep; 18(9):1312-3. PubMed ID: 8612458 [No Abstract] [Full Text] [Related]
11. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus. Shigemoto M; Yoshimasa Y; Yamamoto Y; Hayashi T; Suga J; Inoue G; Okamoto M; Jingami H; Tsuda K; Yamamoto T; Yagura T; Oishi M; Tsujii S; Kuzuya H; Nakao K Intern Med; 1998 Mar; 37(3):265-72. PubMed ID: 9617861 [TBL] [Abstract][Full Text] [Related]
12. Multiple tumors in mitochondrial diabetes associated with tRNALeu(UUR) mutation at position 3264. Suzuki Y; Suzuki S; Taniyama M; Muramatsu T; Ohta S; Oka Y; Atsumi Y; Matsuoka K Diabetes Care; 2003 Jun; 26(6):1942-3. PubMed ID: 12766142 [No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene. Awata T; Matsumoto T; Iwamoto Y; Matsuda A; Kuzuya T; Saito T Lancet; 1993 May; 341(8855):1291-2. PubMed ID: 8098444 [No Abstract] [Full Text] [Related]
16. Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271. Suzuki Y; Tsukuda K; Atsumi Y; Goto Y; Hosokawa K; Asahina T; Nonaka I; Matsuoka K; Oka Y Diabetes Care; 1996 Nov; 19(11):1304-5. PubMed ID: 8908402 [No Abstract] [Full Text] [Related]
17. [Diabetes mellitus caused by a A to G transition at 3243 of the mitochondrial gene]. Oka Y Nihon Rinsho; 1998 Jan; 56 Suppl 3():525-9. PubMed ID: 9513473 [No Abstract] [Full Text] [Related]
18. [Mitochondrial diabetes]. Rötig A; Bonnefont JP; Munnich A Journ Annu Diabetol Hotel Dieu; 1997; ():33-42. PubMed ID: 9296988 [No Abstract] [Full Text] [Related]
19. Age of onset possibly associated with the degree of heteroplasmy in two male siblings with diabetes mellitus having an A to G transition at 3243 of mitochondrial DNA. Kato Y; Miura Y; Inagaki A; Itatsu T; Oiso Y Diabet Med; 2002 Sep; 19(9):784-6. PubMed ID: 12207817 [TBL] [Abstract][Full Text] [Related]
20. Cardiomyopathies and mitochondrial DNA mutations. Takeda N Mol Cell Biochem; 1997 Nov; 176(1-2):287-90. PubMed ID: 9406174 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]