Minami N - Search Results

1

Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis.

Ikezawa M, Minami N, Takahashi M, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Among authors: minami n. Brain Dev. 1998 Apr;20(3):165-8. doi: 10.1016/s0387-7604(98)00012-6. Brain Dev. 1998. PMID: 9628192

2

MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathy.

Nishino I, Minami N, Kobayashi O, Ikezawa M, Goto Y, Arahata K, Nonaka I. Nishino I, et al. Among authors: minami n. Neuromuscul Disord. 1998 Oct;8(7):453-8. doi: 10.1016/s0960-8966(98)00075-3. Neuromuscul Disord. 1998. PMID: 9829274 Free article.

3

Differences in evoked potential characteristics between DRPLA patients and patients with progressive myoclonic epilepsy: preliminary findings indicating usefulness for differential diagnosis.

Kasai K, Onuma T, Kato M, Kato T, Takeya J, Sekimoto M, Watanabe K, Minami N, Goto Y, Minabe Y. Kasai K, et al. Among authors: minami n. Epilepsy Res. 1999 Oct;37(1):3-11. doi: 10.1016/s0920-1211(99)00028-5. Epilepsy Res. 1999. PMID: 10515170

4

Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.

Minami N, Nishino I, Kobayashi O, Ikezoe K, Goto Y, Nonaka I. Minami N, et al. J Neurol Sci. 1999 Dec 1;171(1):31-7. doi: 10.1016/s0022-510x(99)00245-2. J Neurol Sci. 1999. PMID: 10567047

5

Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)(11) in PABP2 gene.

Nagashima T, Kato H, Kase M, Maguchi S, Mizutani Y, Matsuda K, Chuma T, Mano Y, Goto Y, Minami N, Nonaka I, Nagashima K. Nagashima T, et al. Among authors: minami n. Neuromuscul Disord. 2000 Mar;10(3):173-7. doi: 10.1016/s0960-8966(99)00104-2. Neuromuscul Disord. 2000. PMID: 10734263

6

A novel congenital myopathy with apoptotic changes.

Ikezoe K, Yan C, Momoi T, Imoto C, Minami N, Ariga M, Nihei K, Nonaka I. Ikezoe K, et al. Among authors: minami n. Ann Neurol. 2000 Apr;47(4):531-6. Ann Neurol. 2000. PMID: 10762169

7

[Molecular genetic diagnosis of muscle diseases].

Minami N, Nonaka I. Minami N, et al. Nihon Rinsho. 1999 Dec;57 Suppl:691-5. Nihon Rinsho. 1999. PMID: 10778221 Review. Japanese. No abstract available.

8

Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy.

Chae J, Minami N, Jin Y, Nakagawa M, Murayama K, Igarashi F, Nonaka I. Chae J, et al. Among authors: minami n. Neuromuscul Disord. 2001 Sep;11(6-7):547-55. doi: 10.1016/s0960-8966(01)00197-3. Neuromuscul Disord. 2001. PMID: 11525884

9

Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy.

Minami N, Ikezoe K, Kuroda H, Nakabayashi H, Satoyoshi E, Nonaka I. Minami N, et al. Neuromuscul Disord. 2001 Nov;11(8):699-702. doi: 10.1016/s0960-8966(01)00227-9. Neuromuscul Disord. 2001. PMID: 11595511

10

[Recent advances in limb-girdle muscular dystrophy research].

Nonaka I, Minami N, Chae J, Hayashi YK, Nishino I, Arahata K. Nonaka I, et al. Among authors: minami n. Rinsho Shinkeigaku. 2001 Dec;41(12):1194-7. Rinsho Shinkeigaku. 2001. PMID: 12235836 Review. Japanese.

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