Nishino I - Search Results

1

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. Among authors: nishino i. J Neurol Sci. 1999 Dec 1;171(1):31-7. doi: 10.1016/s0022-510x(99)00245-2. J Neurol Sci. 1999. PMID: 10567047

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. Neuromuscul Disord. 1998 Oct;8(7):453-8. doi: 10.1016/s0960-8966(98)00075-3. Neuromuscul Disord. 1998. PMID: 9829274 Free article.

3

Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.

Ikezawa M, Nishino I, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Among authors: nishino i. Hum Mutat. 1999;13(2):170. doi: 10.1002/(SICI)1098-1004(1999)13:2<170::AID-HUMU12>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10094556

4

Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.

Ozawa M, Nishino I, Horai S, Nonaka I, Goto YI. Ozawa M, et al. Among authors: nishino i. Muscle Nerve. 1997 Mar;20(3):271-8. doi: 10.1002/(SICI)1097-4598(199703)20:3<271::AID-MUS2>3.0.CO;2-8. Muscle Nerve. 1997. PMID: 9052804

5

A new congenital muscular dystrophy with mitochondrial structural abnormalities.

Nishino I, Kobayashi O, Goto Y, Kurihara M, Kumagai K, Fujita T, Hashimoto K, Horai S, Nonaka I. Nishino I, et al. Muscle Nerve. 1998 Jan;21(1):40-7. doi: 10.1002/(sici)1097-4598(199801)21:1<40::aid-mus6>3.0.co;2-g. Muscle Nerve. 1998. PMID: 9427222

6

Sarcolemmopathy: muscular dystrophies with cell membrane defects.

Ozawa E, Nishino I, Nonaka I. Ozawa E, et al. Among authors: nishino i. Brain Pathol. 2001 Apr;11(2):218-30. doi: 10.1111/j.1750-3639.2001.tb00394.x. Brain Pathol. 2001. PMID: 11303797 Free PMC article. Review.

7

[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: nishino i. Rinsho Shinkeigaku. 2001 Dec;41(12):1194-7. Rinsho Shinkeigaku. 2001. PMID: 12235836 Review. Japanese.

8

Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness.

Ishikawa H, Sugie K, Murayama K, Ito M, Minami N, Nishino I, Nonaka I. Ishikawa H, et al. Among authors: nishino i. Neurology. 2002 Sep 24;59(6):920-3. doi: 10.1212/wnl.59.6.920. Neurology. 2002. PMID: 12297580

9

A unique case of limb-girdle muscular dystrophy type 2A carrying novel compound heterozygous mutations in the human CAPN3 gene.

Matsubara E, Tsuchiya A, Minami N, Nishino I, Pappolla MA, Shoji M, Abe K. Matsubara E, et al. Among authors: nishino i. Eur J Neurol. 2007 Jul;14(7):819-22. doi: 10.1111/j.1468-1331.2007.01808.x. Eur J Neurol. 2007. PMID: 17594342

10

Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.

Okada M, Kawahara G, Noguchi S, Sugie K, Murayama K, Nonaka I, Hayashi YK, Nishino I. Okada M, et al. Among authors: nishino i. Neurology. 2007 Sep 4;69(10):1035-42. doi: 10.1212/01.wnl.0000271387.10404.4e. Neurology. 2007. PMID: 17785673

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