Murakami T - Search Results

1

Encephalopathy caused by visceral larva migrans due to Ascaris suum.

Inatomi Y, Murakami T, Tokunaga M, Ishiwata K, Nawa Y, Uchino M. Inatomi Y, et al. Among authors: murakami t. J Neurol Sci. 1999 Apr 1;164(2):195-9. doi: 10.1016/s0022-510x(99)00078-7. J Neurol Sci. 1999. PMID: 10402033

2

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. J Neurol Sci. 1996 Oct;142(1-2):111-3. doi: 10.1016/0022-510x(96)00165-7. J Neurol Sci. 1996. PMID: 8902729

3

Decrease in Cu/Zn- and Mn-superoxide dismutase activities in brain and spinal cord of patients with amyotrophic lateral sclerosis.

Uchino M, Ando Y, Tanaka Y, Nakamura T, Uyama E, Mita S, Murakami T, Ando M. Uchino M, et al. Among authors: murakami t. J Neurol Sci. 1994 Dec 1;127(1):61-7. doi: 10.1016/0022-510x(94)90136-8. J Neurol Sci. 1994. PMID: 7699393

4

Parkinsonian symptoms as an initial manifestation in a Japanese patient with acquired immunodeficiency syndrome and Toxoplasma infection.

Murakami T, Nakajima M, Nakamura T, Hara A, Uyama E, Mita S, Matsushita S, Uchino M. Murakami T, et al. Intern Med. 2000 Dec;39(12):1111-4. doi: 10.2169/internalmedicine.39.1111. Intern Med. 2000. PMID: 11197803 Free article. Review.

5

Genetic abnormalities and pathogenesis of familial amyloidotic polyneuropathy.

Murakami T, Uchino M, Ando M. Murakami T, et al. Pathol Int. 1995 Jan;45(1):1-9. doi: 10.1111/j.1440-1827.1995.tb03373.x. Pathol Int. 1995. PMID: 7704238 Review.

6

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: murakami t. Ann Neurol. 1994 Apr;35(4):413-9. doi: 10.1002/ana.410350407. Ann Neurol. 1994. PMID: 8154867

7

High signal in the spinal cord on T2-weighted images in rapidly progressive tropical spastic paraparesis.

Watanabe M, Yamashita T, Hara A, Murakami T, Ando Y, Uyama E, Mita S, Uchino M. Watanabe M, et al. Among authors: murakami t. Neuroradiology. 2001 Mar;43(3):231-3. doi: 10.1007/s002340000449. Neuroradiology. 2001. PMID: 11305756

8

Atypical phenotype of charcot-marie-tooth disease type 1A.

Murakami T, Oomori H, Hara A, Uyama E, Mita S, Uchino M. Murakami T, et al. Muscle Nerve. 1999 Nov;22(11):1593-6. doi: 10.1002/(sici)1097-4598(199911)22:11<1593::aid-mus17>3.0.co;2-h. Muscle Nerve. 1999. PMID: 10514240

9

Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-loxP recombination system in motor neurons of mutant SOD1 transgenic mice.

Yamashita S, Mita S, Arima T, Maeda Y, Kimura E, Nishida Y, Murakami T, Okado H, Uchino M. Yamashita S, et al. Among authors: murakami t. Gene Ther. 2001 Jul;8(13):977-86. doi: 10.1038/sj.gt.3301479. Gene Ther. 2001. PMID: 11438832

10

A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita.

Sasaki R, Ito N, Shimamura M, Murakami T, Kuzuhara S, Uchino M, Uyama E. Sasaki R, et al. Among authors: murakami t. Muscle Nerve. 2001 Mar;24(3):357-63. doi: 10.1002/1097-4598(200103)24:3<357::aid-mus1006>3.0.co;2-e. Muscle Nerve. 2001. PMID: 11353420

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