Kumamoto T - Search Results

1

Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Tokunaga M, Mita S, Murakami T, Kumamoto T, Uchino M, Nonaka I, Ando M. Tokunaga M, et al. Among authors: kumamoto t. Ann Neurol. 1994 Apr;35(4):413-9. doi: 10.1002/ana.410350407. Ann Neurol. 1994. PMID: 8154867

2

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Mita S, Tokunaga M, Kumamoto T, Uchino M, Nonaka I, Ando M. Mita S, et al. Among authors: kumamoto t. Muscle Nerve Suppl. 1995;3:S113-8. doi: 10.1002/mus.880181423. Muscle Nerve Suppl. 1995. PMID: 7603511 Review.

3

Facioscapulohumeral muscular dystrophy with chromosome 9p deletion.

Ueyama H, Kumamoto T, Mita S, Kimura E, Nakagawa M, Uchino M, Ando M. Ueyama H, et al. Among authors: kumamoto t. Neurology. 1996 Feb;46(2):566-9. doi: 10.1212/wnl.46.2.566. Neurology. 1996. PMID: 8614537

4

Single muscle fiber analysis of myoclonus epilepsy with ragged-red fibers.

Mita S, Tokunaga M, Uyama E, Kumamoto T, Uekawa K, Uchino M. Mita S, et al. Among authors: kumamoto t. Muscle Nerve. 1998 Apr;21(4):490-7. doi: 10.1002/(sici)1097-4598(199804)21:4<490::aid-mus7>3.0.co;2-4. Muscle Nerve. 1998. PMID: 9533783

5

Exonic trinucleotide repeats and expression of androgen receptor gene in spinal cord from X-linked spinal and bulbar muscular atrophy.

Nakamura M, Mita S, Murakami T, Uchino M, Watanabe S, Tokunaga M, Kumamoto T, Ando M. Nakamura M, et al. Among authors: kumamoto t. J Neurol Sci. 1994 Mar;122(1):74-9. doi: 10.1016/0022-510x(94)90054-x. J Neurol Sci. 1994. PMID: 7515106

6

Muscle fiber degradation in distal myopathy with rimmed vacuoles.

Kumamoto T, Ueyama H, Watanabe S, Kominami E, Ando M. Kumamoto T, et al. Acta Neuropathol. 1994;87(2):143-8. doi: 10.1007/BF00296183. Acta Neuropathol. 1994. PMID: 8171964

7

Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.

Murakami T, Mita S, Tokunaga M, Maeda H, Ueyama H, Kumamoto T, Uchino M, Ando M. Murakami T, et al. Among authors: kumamoto t. J Neurol Sci. 1996 Oct;142(1-2):111-3. doi: 10.1016/0022-510x(96)00165-7. J Neurol Sci. 1996. PMID: 8902729

8

[A case of chronic progressive external ophthalmoplegia presenting as inflammatory myopathy].

Fujimoto S, Ueyama H, Mita S, Kumamoto T, Tsuda T. Fujimoto S, et al. Among authors: kumamoto t. Rinsho Shinkeigaku. 1998 Mar;38(3):228-32. Rinsho Shinkeigaku. 1998. PMID: 9711119 Review. Japanese.

9

A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy.

Murakami T, Atsumi T, Maeda S, Tanase S, Ishikawa K, Mita S, Kumamoto T, Araki S, Ando M. Murakami T, et al. Among authors: kumamoto t. Biochem Biophys Res Commun. 1992 Aug 31;187(1):397-403. doi: 10.1016/s0006-291x(05)81506-2. Biochem Biophys Res Commun. 1992. PMID: 1520326

10

Neurologic features of chronic Minamata disease (organic mercury poisoning) certified at autopsy.

Uchino M, Okajima T, Eto K, Kumamoto T, Mishima I, Ando M. Uchino M, et al. Among authors: kumamoto t. Intern Med. 1995 Aug;34(8):744-7. doi: 10.2169/internalmedicine.34.744. Intern Med. 1995. PMID: 8563113 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

634 results

Search Page

Filters