Kumamoto T - Search Results

1

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

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

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

4

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

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

[Oculopharyngeal muscular dystrophy in a Japanese family].

Tokunaga M, Uyama E, Tooya M, Kumamoto T, Araki S. Tokunaga M, et al. Among authors: kumamoto t. Rinsho Shinkeigaku. 1990 Jan;30(1):29-36. Rinsho Shinkeigaku. 1990. PMID: 2184963 Review. Japanese.

7

Prevalence studies of multiple sclerosis, myasthenia gravis, and myopathies in Kumamoto district, Japan.

Araki S, Uchino M, Kumamoto T. Araki S, et al. Among authors: kumamoto t. Neuroepidemiology. 1987;6(3):120-9. doi: 10.1159/000110107. Neuroepidemiology. 1987. PMID: 3658081

8

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

9

Clinical and genetic studies of spinocerebellar ataxia type 2 in Japanese kindreds.

Ueyama H, Kumamoto T, Nagao S, Mita S, Uchino M, Tsuda T. Ueyama H, et al. Among authors: kumamoto t. Acta Neurol Scand. 1998 Dec;98(6):427-32. doi: 10.1111/j.1600-0404.1998.tb07325.x. Acta Neurol Scand. 1998. PMID: 9875622

10

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

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