Ando M - Search Results

1

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: ando m. Muscle Nerve Suppl. 1995;3:S113-8. doi: 10.1002/mus.880181423. Muscle Nerve Suppl. 1995. PMID: 7603511 Review.

2

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

3

Polymerase chain reaction fiber analysis and somatic mosaicism in autopsied tissue from a man with Duchenne muscular dystrophy.

Uchino M, Tokunaga M, Yamashita T, Mita S, Hara A, Uyama E, Teramoto H, Naoe H, Ando M. Uchino M, et al. Among authors: ando m. Acta Neuropathol. 1995;90(2):203-7. doi: 10.1007/BF00294322. Acta Neuropathol. 1995. PMID: 7484098

4

In vivo proviral burden and viral RNA expression in T cell subsets of patients with human T lymphotropic virus type-1-associated myelopathy/tropical spastic paraparesis.

Cho I, Sugimoto M, Mita S, Tokunaga M, Imamura F, Ando M. Cho I, et al. Among authors: ando m. Am J Trop Med Hyg. 1995 Oct;53(4):412-8. doi: 10.4269/ajtmh.1995.53.412. Am J Trop Med Hyg. 1995. PMID: 7485696

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: ando m. J Neurol Sci. 1994 Mar;122(1):74-9. doi: 10.1016/0022-510x(94)90054-x. J Neurol Sci. 1994. PMID: 7515106

6

PCR and immunocytochemical analyses of dystrophin-positive fibers in Duchenne muscular dystrophy.

Uchino M, Tokunaga M, Mita S, Uyama E, Ando Y, Teramoto H, Miike T, Ando M. Uchino M, et al. Among authors: ando y, ando m. J Neurol Sci. 1995 Mar;129(1):44-50. doi: 10.1016/0022-510x(94)00245-j. J Neurol Sci. 1995. PMID: 7751844

7

Dystrophin and dystrophin-related protein in the brains of normal and mdx mice.

Uchino M, Yoshioka K, Miike T, Tokunaga M, Uyama E, Teramoto H, Naoe H, Ando M. Uchino M, et al. Among authors: ando m. Muscle Nerve. 1994 May;17(5):533-8. doi: 10.1002/mus.880170511. Muscle Nerve. 1994. PMID: 8159184

8

Muscle fiber degradation in distal myopathy with rimmed vacuoles.

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

9

Oculopharyngeal muscular dystrophy in two unrelated Japanese families.

Uyama E, Nohira O, Chateau D, Tokunaga M, Uchino M, Okabe T, Ando M, Tome FM. Uyama E, et al. Among authors: ando m. Neurology. 1996 Mar;46(3):773-8. doi: 10.1212/wnl.46.3.773. Neurology. 1996. PMID: 8618681

10

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

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