Ogawa M - Search Results

1

A new diagnostic test for VLCAD deficiency using immunohistochemistry.

Ohashi Y, Hasegawa Y, Murayama K, Ogawa M, Hasegawa T, Kawai M, Sakata N, Yoshida K, Yarita H, Imai K, Kumagai I, Murakami K, Hasegawa H, Noguchi S, Nonaka I, Yamaguchi S, Nishino I. Ohashi Y, et al. Among authors: ogawa m. Neurology. 2004 Jun 22;62(12):2209-13. doi: 10.1212/01.wnl.0000130486.54839.15. Neurology. 2004. PMID: 15210884

2

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

Hayashi YK, Ogawa M, Tagawa K, Noguchi S, Ishihara T, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: ogawa m. Neurology. 2001 Jul 10;57(1):115-21. doi: 10.1212/wnl.57.1.115. Neurology. 2001. PMID: 11445638

3

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I. Kim DS, et al. Among authors: ogawa m. Neurology. 2004 Mar 23;62(6):1009-11. doi: 10.1212/01.wnl.0000115386.28769.65. Neurology. 2004. PMID: 15037715

4

[Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].

Oya Y, Segawa M, Ogawa M, Goto Y, Nonaka I, Kawai M. Oya Y, et al. Among authors: ogawa m. Rinsho Shinkeigaku. 2000 May;40(5):452-8. Rinsho Shinkeigaku. 2000. PMID: 11002727 Japanese.

5

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.

Matsuda C, Hayashi YK, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown RH Jr. Matsuda C, et al. Among authors: ogawa m. Hum Mol Genet. 2001 Aug 15;10(17):1761-6. doi: 10.1093/hmg/10.17.1761. Hum Mol Genet. 2001. PMID: 11532985

6

[A patient with dermatomyositis and systemic sclerosis with preferential facioscapulohumeral muscle involvement and fatal cardiomyopathy].

Oya Y, Toyama J, Ogawa M, Nonaka I, Kawai M. Oya Y, et al. Among authors: ogawa m. Rinsho Shinkeigaku. 2001 Jun;41(6):289-95. Rinsho Shinkeigaku. 2001. PMID: 11771157 Japanese.

7

[Adult form of acid maltase deficiency presenting with pattern of muscle weakness resembling facioscapulohumeral dystrophy].

Oya Y, Morita H, Ogawa M, Nonaka I, Tsujino S, Kawai M. Oya Y, et al. Among authors: ogawa m. Rinsho Shinkeigaku. 2001 Jul;41(7):390-6. Rinsho Shinkeigaku. 2001. PMID: 11808348 Japanese.

8

Mutations in the integrin alpha7 gene cause congenital myopathy.

Hayashi YK, Chou FL, Engvall E, Ogawa M, Matsuda C, Hirabayashi S, Yokochi K, Ziober BL, Kramer RH, Kaufman SJ, Ozawa E, Goto Y, Nonaka I, Tsukahara T, Wang JZ, Hoffman EP, Arahata K. Hayashi YK, et al. Among authors: ogawa m. Nat Genet. 1998 May;19(1):94-7. doi: 10.1038/ng0598-94. Nat Genet. 1998. PMID: 9590299

9

[Quantitative evaluation of the effect of 3,4-diaminopyridine in a patient with Lambert-Eaton myasthenic syndrome using dynamic dynamometry].

Oishi K, Oya Y, Yamamoto T, Shigeto H, Ogawa M, Kawai M. Oishi K, et al. Among authors: ogawa m. Rinsho Shinkeigaku. 2001 Aug;41(8):515-8. Rinsho Shinkeigaku. 2001. PMID: 11889838 Japanese.

10

[Therapeutic trial of beta 2-adrenergic agonist clenbuterol in muscular dystrophies].

Oya Y, Ogawa M, Kawai M. Oya Y, et al. Among authors: ogawa m. Rinsho Shinkeigaku. 2001 Oct;41(10):698-700. Rinsho Shinkeigaku. 2001. PMID: 11993192 Clinical Trial. Japanese.

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