Nonaka I - Search Results

1

[Cousins with X-linked recessive myotubular myopathy].

Mori Y, Kaneko S, Nakayama T, Date M, Nakamoto N, Kobayashi M, Sugiura M, Hashira S, Abe T, Hirokawa H, Nonaka I. Mori Y, et al. Among authors: nonaka i. No To Hattatsu. 1997 Jul;29(4):310-4. No To Hattatsu. 1997. PMID: 9248291 Review. Japanese.

2

[Reducing body myopathy--a case report].

Kobayashi Y, Nihei K, Kuwajima K, Nonaka I. Kobayashi Y, et al. Among authors: nonaka i. Rinsho Shinkeigaku. 1992 Jan;32(1):62-7. Rinsho Shinkeigaku. 1992. PMID: 1321016 Review. Japanese.

3

Infantile polymyositis: a case report.

Nagai T, Hasegawa T, Saito M, Hayashi S, Nonaka I. Nagai T, et al. Among authors: nonaka i. Brain Dev. 1992 May;14(3):167-9. doi: 10.1016/s0387-7604(12)80258-0. Brain Dev. 1992. PMID: 1514657

4

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation.

Goto Y, Horai S, Matsuoka T, Koga Y, Nihei K, Kobayashi M, Nonaka I. Goto Y, et al. Among authors: nonaka i. Neurology. 1992 Mar;42(3 Pt 1):545-50. doi: 10.1212/wnl.42.3.545. Neurology. 1992. PMID: 1549215

5

[Ergometric and pathologic study of a family with complex I deficiency].

Tojo M, Ogawa N, Takeuchi M, Toyama J, Torigoe K, Sato S, Takahashi R, Koga Y, Nonaka I. Tojo M, et al. Among authors: nonaka i. No To Hattatsu. 1992 Jan;24(1):20-6. No To Hattatsu. 1992. PMID: 1731824 Japanese.

6

[MELAS without ragged-red fibers: a case report].

Mimaki N, Hasegawa H, Nonaka I. Mimaki N, et al. Among authors: nonaka i. No To Hattatsu. 1991 Nov;23(6):606-11. No To Hattatsu. 1991. PMID: 1760209 Japanese.

7

[A case with MELAS associated with epilepsia partialis continua].

Miyazaki M, Saijo T, Mori K, Tayama M, Naito E, Hashimoto T, Kuroda Y, Nonaka I. Miyazaki M, et al. Among authors: nonaka i. No To Hattatsu. 1991 Jan;23(1):65-70. No To Hattatsu. 1991. PMID: 1899796 Japanese.

8

[A case of facioscapulohumeral muscular dystrophy with infantile spasms, sensorineural deafness and retinal vessel abnormality].

Akiyama C, Suzuki H, Nonaka I. Akiyama C, et al. Among authors: nonaka i. No To Hattatsu. 1991 Jul;23(4):395-9. No To Hattatsu. 1991. PMID: 1908258 Review. Japanese.

9

[Congenital neuromuscular disease with uniform type 1 fibers : a case report].

Araki A, Kurokawa T, Sakuragawa N, Nonaka I. Araki A, et al. Among authors: nonaka i. No To Hattatsu. 1991 May;23(3):295-8. No To Hattatsu. 1991. PMID: 2043374 Japanese.

10

[A case of complex I deficiency with episodic respiratory distress].

Tohyama J, Torigoe K, Sato S, Takahashi R, Suda M, Tojo M, Nonaka I, Koga Y, Tanaka M, Ozawa T. Tohyama J, et al. Among authors: nonaka i. No To Hattatsu. 1990 Jul;22(4):369-75. No To Hattatsu. 1990. PMID: 2119195 Japanese.

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