Uchino M - 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: uchino m. 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: uchino m. 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: uchino 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

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

7

Leber's hereditary optic neuropathy with dystonia in a Japanese family.

Watanabe M, Mita S, Takita T, Goto Y, Uchino M, Imamura S. Watanabe M, et al. Among authors: uchino m. J Neurol Sci. 2006 Apr 15;243(1-2):31-4. doi: 10.1016/j.jns.2005.11.003. Epub 2005 Dec 27. J Neurol Sci. 2006. PMID: 16380132

8

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. Intern Med. 1996 Mar;35(3):189-94. doi: 10.2169/internalmedicine.35.189. Intern Med. 1996. PMID: 8785451 Free article.

9

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. Among authors: uchino m. 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

10

[A case of pericarotid syndrome with retention cyst in ethmoid sinus].

Tokunaga M, Uyama E, Goto A, Ogi K, Uchino M. Tokunaga M, et al. Among authors: uchino m. Rinsho Shinkeigaku. 2000 Jan;40(1):39-43. Rinsho Shinkeigaku. 2000. PMID: 10825799 Japanese.

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