Mita S - Search Results

1

[Single-fiber polymerase chain reaction for detection of mutant mitochondrial DNA].

Tokunaga M, Mita S, Uchino M. Tokunaga M, et al. Among authors: mita s. Nihon Rinsho. 1997 Dec;55(12):3291-4. Nihon Rinsho. 1997. PMID: 9436453 Review. Japanese.

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

3

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

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. 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

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: mita s. Acta Neuropathol. 1995;90(2):203-7. doi: 10.1007/BF00294322. Acta Neuropathol. 1995. PMID: 7484098

6

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

7

Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S. Tokunaga M, et al. Among authors: mita s. Ann Neurol. 1993 Mar;33(3):275-80. doi: 10.1002/ana.410330308. Ann Neurol. 1993. PMID: 7684581

8

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: mita s. J Neurol Sci. 1995 Mar;129(1):44-50. doi: 10.1016/0022-510x(94)00245-j. J Neurol Sci. 1995. PMID: 7751844

9

Increased human T lymphotropic virus type-1 (HTLV-1) proviral DNA in peripheral blood mononuclear cells and bronchoalveolar lavage cells from Japanese patients with HTLV-1-associated myelopathy.

Mita S, Sugimoto M, Nakamura M, Murakami T, Tokunaga M, Uyama E, Araki S. Mita S, et al. Am J Trop Med Hyg. 1993 Feb;48(2):170-7. doi: 10.4269/ajtmh.1993.48.170. Am J Trop Med Hyg. 1993. PMID: 8447519

10

Distribution of dystrophin and dystrophin-associated protein 43DAG (beta-dystroglycan) in the central nervous system of normal controls and patients with Duchenne muscular dystrophy.

Uchino M, Hara A, Mizuno Y, Fujiki M, Nakamura T, Tokunaga M, Hirano T, Yamashita T, Uyama E, Ando Y, Mita S, Ando M. Uchino M, et al. Among authors: mita s. Intern Med. 1996 Mar;35(3):189-94. doi: 10.2169/internalmedicine.35.189. Intern Med. 1996. PMID: 8785451 Free article.

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