Ohtomo M - Search Results

1

[Stability of allantoin and identification of its degradation compounds].

Yamamoto S, Ohtomo M, Komatsu K, Takamatsu T, Matsuoka M. Yamamoto S, et al. Among authors: ohtomo m. Yakugaku Zasshi. 1993 Jul;113(7):515-24. doi: 10.1248/yakushi1947.113.7_515. Yakugaku Zasshi. 1993. PMID: 8366429 Japanese.

2

Mitochondrial DNA 3394 mutation in the NADH dehydrogenase subunit 1 associated with non-insulin-dependent diabetes mellitus.

Hirai M, Suzuki S, Onoda M, Hinokio Y, Ai L, Hirai A, Ohtomo M, Komatsu K, Kasuga S, Satoh Y, Akai H, Toyota T. Hirai M, et al. Among authors: ohtomo m. Biochem Biophys Res Commun. 1996 Feb 27;219(3):951-5. doi: 10.1006/bbrc.1996.0324. Biochem Biophys Res Commun. 1996. PMID: 8645285

3

A new mitochondrial DNA deletion associated with diabetic amyotrophy, diabetic myoatrophy and diabetic fatty liver.

Hinokio Y, Suzuki S, Komatu K, Ohtomo M, Onoda M, Matsumoto M, Hirai S, Sato Y, Akai H, Abe K, et al. Hinokio Y, et al. Among authors: ohtomo m. Muscle Nerve Suppl. 1995;3:S142-9. doi: 10.1002/mus.880181428. Muscle Nerve Suppl. 1995. PMID: 7603516

4

Diabetes with mitochondrial gene tRNALYS mutation.

Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K, et al. Suzuki S, et al. Among authors: ohtomo m. Diabetes Care. 1994 Dec;17(12):1428-32. doi: 10.2337/diacare.17.12.1428. Diabetes Care. 1994. PMID: 7882812

5

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).

Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K, et al. Suzuki S, et al. Among authors: ohtomo m. Diabetologia. 1994 Aug;37(8):818-25. doi: 10.1007/BF00404339. Diabetologia. 1994. PMID: 7988784 Clinical Trial.

6

Mitochondrial deoxyribonucleic acid 3256C-T mutation in a Japanese family with noninsulin-dependent diabetes mellitus.

Hirai M, Suzuki S, Onoda M, Hinokio Y, Hirai A, Ohtomo M, Chiba M, Kasuga S, Hirai S, Satoh Y, Akai H, Miyabayashi S, Toyota T. Hirai M, et al. Among authors: ohtomo m. J Clin Endocrinol Metab. 1998 Mar;83(3):992-4. doi: 10.1210/jcem.83.3.4643. J Clin Endocrinol Metab. 1998. PMID: 9506761

7

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. Suzuki S, et al. Among authors: ohtomo m. Diabetologia. 1998 May;41(5):584-8. doi: 10.1007/s001250050950. Diabetologia. 1998. PMID: 9628277 Clinical Trial.

8

Oxidative damage to mitochondrial DNA and its relationship to diabetic complications.

Suzuki S, Hinokio Y, Komatu K, Ohtomo M, Onoda M, Hirai S, Hirai M, Hirai A, Chiba M, Kasuga S, Akai H, Toyota T. Suzuki S, et al. Among authors: ohtomo m. Diabetes Res Clin Pract. 1999 Sep;45(2-3):161-8. doi: 10.1016/s0168-8227(99)00046-7. Diabetes Res Clin Pract. 1999. PMID: 10588369

9

Urinary chiro-inositol excretion is an index marker of insulin sensitivity in Japanese type II diabetes.

Suzuki S, Kawasaki H, Satoh Y, Ohtomo M, Hirai M, Hirai A, Hirai S, Onoda M, Matsumoto M, Hinokio Y, et al. Suzuki S, et al. Among authors: ohtomo m. Diabetes Care. 1994 Dec;17(12):1465-8. doi: 10.2337/diacare.17.12.1465. Diabetes Care. 1994. PMID: 7882818

10

Effect of manidipine and delapril on insulin sensitivity in type 2 diabetic patients with essential hypertension.

Suzuki S, Ohtomo M, Satoh Y, Kawasaki H, Hirai M, Hirai A, Hirai S, Onoda M, Hinokio Y, Akai H, Toyota T. Suzuki S, et al. Among authors: ohtomo m. Diabetes Res Clin Pract. 1996 Jun;33(1):43-51. doi: 10.1016/0168-8227(96)01273-9. Diabetes Res Clin Pract. 1996. PMID: 8877275

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